Transcription factors involved in abiotic stress responses in Maize (Zea mays L.) and their roles in enhanced productivity in the post genomics era

View article
Plant Biology
Note that a Preprint of this article also exists, first published February 23, 2019.


Abiotic stresses, for instance drought, salinity, cold, high temperatures, and mineral toxicity, are the main cause of major crop yield reductions worldwide, reducing expected average yields of the major crops by more than 50% (Prasad et al., 2011; Mahalingam, 2015). Plants are sessile beings that are continuously exposed to various changes in the environmental conditions. Variations in the environment involving both biotic and abiotic stresses have negative effects on economically important crops like maize (Ramegowda & Senthil-Kumar, 2015). Evolutionary changes have helped many plants adapt to different adverse conditions. Some species show a marked increase in tolerance to various abiotic stresses compared to others (Phukan et al., 2014). Due to global warming and the climatic abnormalities accompanying it, the frequencies of combined biotic and abiotic stresses have significantly increased, leading to reduced growth and yield of the major crops worldwide (Mittler, 2006; Pandey, Ramegowda & Senthil-Kumar, 2015; Ramegowda & Senthil-Kumar, 2015). Moreover, continuous manifestations of abiotic stresses such as heat and drought together, has led to severe reductions in crop yields as opposed to when these stresses occur separately during the different growth stages (Mittler, 2006; Prasad et al., 2011).

Maize (Zea mays ssp. Mays L.) is one of the most important cereal crops cultivated worldwide (particularly in Africa and South America). Global maize production increased from 255 million tons in 1968 to 1,134 million tons in 2017 representing an average annual growth of 3.46% ( Maize production has significantly increased in both the developing countries and the developed countries (Wang et al., 2013).

Maize is a staple food in many parts of the world; it is consumed directly by humans, used for animal feed, and in other maize products such as corn syrup and corn starch. In the last century, maize has been utilized as a model system in the study of various biological events and systems including paramutation, transposition, allelic diversity, and heterosis (Bennetzen & Hake, 2009). Recently, maize has been identified as a potential sustainable feedstock, as well as a model system for research in the bioenergy and biofuel industries (Perlack et al., 2005). Continuous studies in maize genetics has led to further understanding of other related C4 grasses such as Elephant grass (Miscanthus gigantus) and switchgrass (Panicum virgatum) as scientists aim to develop and domesticate these plants (Perlack et al., 2005). However, maize belts around the world which range from the latitude 40° South to the latitude 58° North are exposed to continuous effects of both biotic and abiotic stresses (Gong et al., 2014). Abiotic stresses, like salinity, drought, nutrient deficiency, and high and low temperatures are the major environmental factors that negatively influence maize production. In particular, intense waterlogging, extreme temperatures, and drought have significantly affected maize yields (Ahuja et al., 2010).

Plants must cope with a variety of abiotic stresses including extreme temperatures, heavy metals, osmotic stresses, and high light intensity. Under stress, accumulation of some metabolites positively regulates plants response to both abiotic and biotic stresses thus protecting plants from multiple stresses (Rasmussen et al., 2013; Suzuki et al., 2014). Changes in ions fluxes, callose accumulation, phytohormones, and reactive oxygen species (ROS) are the first responses induced to tackle the stresses, leading to metabolic reprogramming in the plants defenses (Bartoli et al., 2013).

Reactive oxygen species such as hydrogen peroxide (H2O2) and superoxide (•O−2) which are produced due to oxidative stresses, inhibit photosynthesis and cause vast cellular destruction (Allan & Fluhr, 2007). ROS are normally removed rapidly by antioxidative mechanisms, although this removal can be hindered by the stresses leading to an increase in ROS concentration inside the cells, and further increasing the damage caused (Allan & Fluhr, 2007).

Another pathway involved in abiotic stress responses in plants is the mitogen-activated protein kinase (MAPK) cascades. MAPK cascades are activated following the recognition and perception of stress stimuli and control the stress response pathways (Wurzinger et al., 2011). They are highly conserved in eukaryotes and are responsible for signal transduction in various cellular processes under different biotic and abiotic stress responses. Because MAPKs are involved in various stress responses, they play a main role in the combination of biotic and abiotic stresses (Amajová et al., 2013).

Additionally, hormone signaling in plants is another important pathway involved in biotic and abiotic stress responses and the primary hormone involved is abscisic acid (ABA). An increase in ABA concentration in plants under abiotic stress modulates the abiotic stress-regulation network (Xiong, Schumaker & Zhu, 2002), while biotic stress is mediated by antagonism in other stress hormones such as jasmonic-acid (JA)/ethylene (ET) and salicylic acid (SA; Liu et al., 2008). The role of ABA in abiotic stress responses has been widely described throughout this review.

Plants do not respond to multiple stresses by way of a linear pathway. The responses are complex circuits involving various pathways in tissues, cellular specific compartments, and the interactions of signaling molecules in controlling a particular response to a stimulus (Dombrowski, 2003). Due to abiotic stresses, numerous proteins, and gene transcripts are altered through the regulation of protein turnover and gene expression (Jiang et al., 2007; Wong et al., 2006).

In this review, we will briefly describe the main transcription factor (TF) families and the interactions of these TFs with the cis-acting elements (CREs) which are present in the promoter regions of stress responsive genes. Even though TF regulons have been described recently by (Gahlaut et al., 2016; Joshi et al., 2016), this review will focus on TFs involved in abiotic stress tolerance with a specific focus on maize. We will also focus on new ways of increasing production of maize by utilizing currently available genomic information, tools, and data.

Survey methodology

All published manuscripts cited in this review were obtained from different databases including Pubmed, Web of Science, EBSCO, Google Scholar, research gate, Science Direct, SCOPUS, JSTOR, SciELO, and Semantic Scholar. Keywords such as “maize stress tolerance,” “TFs involved in abiotic stress responses,” “abiotic stress,” “TF downstream genes,” and “regulons involved in abiotic stress” were searched between January 10 and October 25, 2018. We have critically analyzed articles to provide an in-depth and comprehensive research trend focusing on the TFs involved in abiotic stress tolerance in maize. Furthermore, we have provided perspectives on the latest research as well as previous findings with focus on TF families involved in abiotic stress responses in maize.

Functions of transcription factors

Abiotic stress-induced genes are generally classified into two main groups based on their protein products. One type includes the genes coding for products which directly allow cells to resist environmental stresses for instance osmotic regulatory protein, late embryogenesis abundant (LEA) protein, enzymes synthesizing proline, betamine, malondialdehyde (MDA), and other osmotic regulators and anti-freezing proteins (Ciarmiello et al., 2011). The second type of genes are regulatory proteins which operate in the signal transduction networks, for example, molecular chaperones, functional proteins, and TFs or kinases (Song, Li & Hou, 2013; Ciarmiello et al., 2011).

Networks of TFs together with transcription factor binding sites (TFBS) directly control transcriptional regulation of plant genes (Chaves & Oliveira, 2004). TFs are proteins usually consisting of two domains, namely (1) the DNA binding domain (DB) and (2) an activation domain (AD). A TF binds to the cis-acting element (TF binding site) located in the promoter region of a stress-induced gene with the support of a DB domain (Yamasaki et al., 2013). This event brings the AD close to the target gene leading to repression or activation of this gene. A large percentage of genes in the plant genome (nearly 10%) essentially encode for TFs (Franco-Zorrilla et al., 2014). TFs activate or repress the activity of RNA polymerase, leading to gene regulation. TFs can be categorized into various families based on their DNA DBs (Riechmann et al., 2000). Since abiotic stresses are quantitative traits that might require regulation of several genes including the TF genes, and since a single TF may regulate several genes that are involved in abiotic stress tolerance. A detailed study of all TFs associated with abiotic stress regulatory mechanisms in maize will be significantly rewarding. For example, Xu et al. (2006) successfully converted flood sensitive rice genotypes into flood-tolerant varieties by introgression of the sub1 locus which encodes an (ET response factor) TF, leading to the induction of about 900 stress-responsive genes.

Transcription factor DNA-DBs are strongly conserved between species, to the extent of using these characteristics to classify the TFs into various families (Fig. 1). These families differ among plant species in that different plant systems have between 26 and 83 TFs families (Jin et al., 2014). In Arabidopsis, for instance, approximately 34 families consisting of 1,533 TFs have so far been classified (Riechmann et al., 2000). Additionally, in Arabidopsis and many other plants, transcriptome data revealed a number of pathways which respond to abiotic stresses independently, pointing to the possibility that susceptibility or tolerance of both biotic and abiotic stresses are controlled by a sophisticated gene regulatory network (GRN) at the transcriptome level (Umezawa et al., 2006).

Gene expression and abiotic stress signal perception in plants.

Figure 1: Gene expression and abiotic stress signal perception in plants.

A diagrammatic representation of gene expression and abiotic stress signal perception in plants via ABA-independent and ABA-dependent pathways (modified from Gahlaut et al., 2016; Khan et al., 2018). Abbreviations: Abscisic acid (ABA), Reactive oxygen species (ROS), myeloblastosis oncogene (MYB), myelocytomatosis oncogene (MYC), Zinc-finger homeodomain (ZF-HD) regulon, ABA-responsive element binding protein (AREB), ABA-independent regulons include the NAC (CUC, NAM, and ATAF), The cis-acting element (DRE), ABA-binding factor (ABF), The cis-acting element (CRE), Dehydration responsive element binding proteins (DREBs), C-repeat (CRT), (ZFR) zinc finger RNA binding protein, (NARC) NAC recognition site, (MYBRS) MYB recognition site, (MYCRS) MYC recognition site, Nuclear transcription factor Y (NF-Y), Heat Shock Factors (HSFs), Inducer of CBF Expression (ICE).

Abscisic acid is the principal hormone involved in the coordination of abiotic stress in plants (Fig. 1). This hormone regulates a complex gene regulatory system that enables plants to handle decreased moisture availability (Cutler et al., 2010). ABA-dependent gene activation pathways were identified as pathways which determine stress tolerance by the induction of at least two separate regulons: the first one is the myeloblastosis oncogene (MYB)/myelocytomatosis oncogene (MYC) regulon, and the second one is the ABA-responsive element binding protein/ABA-binding factor (AREB/ABF) (Abe et al., 1997; Saibo, Lourenço & Oliveira, 2009) (Fig. 1). ABA-independent regulons include the NAC (CUC, NAM, and ATAF) and the zinc-finger homeodomain (HD) regulon (Nakashima, Ito & Yamaguchi-Shinozaki, 2009; Saibo, Lourenço & Oliveira, 2009) (Fig. 1).

The different stress tolerance responsive TFs normally function independently, although there is a possibility that some level of cross-link occurs between these TFs (Fig. 2). Many studies have shown that ABA-independent and ABA-dependent pathways might converge at several unexpected points. This points of convergence represent transcriptional repressors and enhancers interacting indirectly or directly with DRE/C repeat and ABA-responsive element (ABRE) and hence initiate synergistic interactions between the ABA response and osmotic stress (Fig. 2).

Cross-talk network among cis-acting elements and transcription factors.

Figure 2: Cross-talk network among cis-acting elements and transcription factors.

Cross-talk network between cis-acting elements and TFs in the ABA-independent and ABA-dependent pathways during abiotic stress. Broken arrows indicate the protein-protein interactions. Thick green arrows show the major pathways which regulate many downstream genes (modified from Yamaguchi-Shinozaki & Shinozaki, 2006).

The above mentioned TF families have been studied in detail in a number of important food crops and also in model plant systems including; Arabidopsis thaliana, Oryza sativa, Triticum aestivum, Sorghum bicolor, Vitis vinifera, Hordeum vulgare, Solanum tuberosum, and Brassica napus. Recent studies have shown the functions of abiotic stress-responsive TFs, and their potential roles to be used in future for purposes of molecular breeding and improvement of different crop varieties.

Much progress has been achieved in our understanding of transcriptional regulation, signal transduction, and gene expression in plant responses to abiotic stresses (Zhu et al., 2010). In rice, for example, overexpression of a NAC TF encoding gene, SNAC1, resulted in increased yields and increased tolerance to drought in transgenic plants (Hu et al., 2006). Overexpression of a Glycine soja NAC TF designated as GsNAC019 in transgenic Arabidopsis resulted in plants that were tolerant to alkaline stress at both the seedling and mature stages although the transgenic plants had reduced sensitivity to ABA (Cao et al., 2017). Similarly, functional analysis of a Pyrus betulifolia NAC TF gene designated as PbeNAC1, revealed that this gene is involved in the regulation of cold and drought stress tolerance (Jin et al., 2017). Additionally, a chickpea (Cicer arietinum) stress associated TF, CarNAC4 was linked with reduced MDA content and water stress rates in response to salinity and drought stress respectively (Yu et al., 2016).

Ramakrishna et al. (2018) showed that overexpression of a finger millet bZIP TF gene EcbZIP17 in tobacco plants resulted in higher germination rate, increased biomass, and increased survival rate in the transgenic plants. Furthermore, the transgenic tobacco plants also showed increased seed yields compared to the control plants. Likewise, Xu et al. (2006) showed that transgenic Arabidopsis and soybean seedlings overexpressing a soybean bZIP TF designated as GmbZIP110 had improved salt tolerance, suggesting that GmbZIP110 functions as a positive regulator involved in salt stress tolerance. Functional analysis of GmbZIP110 in transgenic Arabidopsis revealed that this gene could bind to the ACGT motif and regulate many downstream target genes (Cao et al., 2017). Elsewhere, overexpression of an Arabidopsis bZIP TF designated as ABF3 in transgenic alfalfa (Medicago sativa) under the command of a sweet potato oxidative stress-inducible promoter SWPA2, resulted in improved growth under drought stress (Wang et al., 2016c). In hot pepper (Capsicum annuum), overexpression of a bZIP encoding gene CaBZ1 in transgenic potato significantly improved dehydration stress tolerance without any detrimental effects on plant growth or yield (Moon et al., 2015).

Overexpression of OsMYB55, a rice MYB encoding gene in transgenic maize resulted in improved plant growth as well as decreased negative effects of drought and high temperature (Casaretto et al., 2016). Wei et al. (2017) demonstrated that CiMYB3 and CiMYB5 cloned from Cichorium intybus were both involved in the fructan pathway degradation in response to various abiotic stresses. In banana (Musa paradisiaca), overexpression of an MYB TF gene designated as MpMYBS3 significantly improved tolerance to cold stress in transgenic plants (Dou et al., 2015). Elsewhere, a MYB TF gene designated as MtMYBS from Medicago truncatula was able to enhance salt and drought tolerance in transgenic Arabidopsis by improving the primary root growth (Dong et al., 2017). Likewise, overexpression of GaMYB62L from cotton (Gossypium arboreum) in transgenic Arabidopsis resulted in enhanced drought tolerance (Butt et al., 2017).

The exogenous expression of AtDREB1A (dehydration responsive element binding proteins (DREB)) gene from Arabidopsis in transgenic Salvia miltiorrhiza resulted in plants with higher antioxidant activities and photosynthetic rates under drought stress (Wei et al., 2016). Elsewhere, overexpression of SbDREB2A from Salicornia brachita in transgenic tobacco resulted in improved growth and seed germination under hyperionic and hyperosmotic stresses (Gupta, Jha & Agarwal, 2014). Zhang et al. (2015) cloned SsDREB protein from Suaeda salsa and showed that this protein enhances the photosynthesis rate in transgenic tobacco plants under drought and salt stresses.

In the WYKY TF gene family, OsWRKY71 from rice was found to act as a positive regulator to cold stress tolerance by regulating several downstream genes like WSI76 and OsTGFR (Kim et al., 2016). Virus-induced gene silencing of the GhWRKY6 gene from cotton (Gossypium hirsutum) led to increased sensitivity to various abiotic stresses in the silenced plants (Ullah et al., 2017). Elsewhere, SIDRW1 and SLWRKY39 which are WRKY TFs were found to confer both abiotic and biotic stress tolerance in tomato (Solanum lycopersicum) by activating both abiotic stress and pathogenesis-related downstream genes (Liu et al., 2014a; Sun et al., 2015).

Transcription factors and regulons involved in abiotic stress regulation from other TF families have also been identified and described. For instance, in Populus euphratica, exogenous expression of PeHLH35 belonging to the bHLH TF family resulted in significant improvement in water deficit tolerance through changes in several physiological processes such as stomatal density and transcription rate (Dong et al., 2014). In tomato, overexpression of a cycling Dof factor (CDF) TF designated as CDF3 resulted in increased biomass production and higher yields in transgenic tomato plants under salt stress (Renau-Morata et al., 2017).

TFs and the specific target genes involved in abiotic stress tolerance in maize

MYC/MYB regulon

The MYC/MYB families of TF proteins have diverse functions and are found in both animals and plants (Abe et al., 2003). Both MYB/MYC TFs participate in the ABA-dependent pathway involved in abiotic stress signaling (Fig. 1). The first MYB TF gene in plants was identified in Maize and was designated as C1, it codes for a c-MYB like TF that is involved in the biosynthesis of anthocyanin (Paz-Ares et al., 1987). In the MYB family, each TF consists of an MYB domain containing 1–3 imperfect repeats and is made up of around 52 amino acid residues with a helix-turn-helix conformation which interposes inside the major grooves of DNA (Yanhui et al., 2006). Both MYB and MYC TFs are usually involved in making up the common regulons known as the MYB/MYC regulons (Gahlaut et al., 2016).

In the maize genome, Du et al. (2013) reported 72 MYB related proteins. Chen et al. (2017) analyzed the expression profiles of 46 MYB genes from maize, in response to various abiotic stresses and found 22 genes that responded to the different stress conditions. Additionally, 16 of these genes were induced in response to a minimum of two stresses. These results suggesting that these genes could take part in signal transduction pathways involved in abiotic stress responses. Additionally, the function of ZmMYB30 which was significantly up-regulated under drought, salt, and ABA stresses was further analyzed (Chen et al., 2017) (Table 1). Exogenous expression of ZmMYB30 in Arabidopsis stimulated tolerance to salt and elevated the expression of eight abiotic stress corresponding genes (ABF3, ATGolS2, AB15, DREB2A, RD20, RD29B, RD29A, and MYB2) enabling transgenic plants to be more tolerant to adverse environmental conditions (Chen et al., 2017) (Table 1). Moreover, another six genes (RD22, RbohD, P5CS1, RAB18, RbohF, and LEA14) were either unchanged or slightly elevated in the transgenic Arabidopsis plants.

Table 1:
Abiotic stress-related TF families, together with the specific TFs in Maize.
Family TFs in maize Cis-element recognition Stress response Downstream genes References
DREB/CBF ZmDREB2A (DRE) TACCGACAT Salt, heat, drought, cold rd29A, rd29B, ZmGOLS2 Qin et al. (2007)
ZmDBP3 (DRE) TACCGACAT Cold, salt U Wang & Dong (2009) and Chang & Yin (2009)
ZmDREB1A (DRE/CRT) G/ACCGAC Drought, cold KIN1, KIN2, COR15A, etc Qin et al. (2004)
ZmDBF3 N/A Salt, drought, freezing U Zhou et al. (2016)
ZmDBP4 (DRE/CRT) G/ACCGAC Cold, drought U Wang, Yang & Yang (2011)
ZmDREB2.7 (DRE) A/GCCGAC Drought U Liu et al. (2013)
MYB/MYC ZmMYB30 (MYBR) TAACNA/G Salt, drought, ABA RD20, RD29A, RbohD, etc Chen et al. (2017)
ZmMYB36 N/A Salt, drought, ABA U Chen et al. (2017)
ZmMYB95 N/A Salt, drought, ABA U Chen et al. (2017)
ZmMYB53 N/A Cold U Chen et al. (2017)
ZmMYB31 N/A Sensitivity to UV radiation ZmF5H, ZmCOMT, C3H, and ZmActin Fornalé et al. (2010)
ZmMYB-R1 N/A Cold, high salinity, drought, ABA, and heat U Liu et al. (2012)
bZIP ZmbZIP60 (ABRE) ACGTGGC Dehydration, high salinity, ABA U Wang et al. (2012)
Heat stress U Li et al. (2018)
ZmbZIP17 N/A Drought, ABA, heat, salt U Jia et al. (2009)
ZmbZIP54 and ZmbZIP107 (ABRE) ACGTGGC Lead (Pb) U Zhang et al. (2017a)
mlip15 (ABRE) ACGTGGC Low temperature, salt, ABA U Kusano et al. (1995)
ZmbZIP72 (ABRE) ACGTGGC ABA, drought, high salinity Rab18, rd29B, HIS1-3, etc Ying et al. (2012)
ABP9 (ABRE) (C/T) ACGTGGC ABA, drought, H2O2, salt KIN1, COR15A, PP2C, AZF2, etc Zhang et al. (2011)
ZmbZIP4 (ABRE) (C/T) ACGTGGC Heat, cold, salinity, and ABA ZmLEA2, ZmRD20, ZMRab18, ZmGEA6, etc Ma et al. (2018)
NAC ZmSNAC1 N/A Low temperature, ABA, high salinity, drought U Lu et al. (2012)
ZmNAC55 N/A High salinity, cold, drought, ABA RD29B, LEA14, RD17, ZAT10, etc Mao et al. (2016)
Zma006493 N/A Drought U Lu et al. (2015)
Zma000584 N/A Drought, cold U Lu et al. (2015)
Zma001259 N/A Drought, salt, cold U Lu et al. (2015)
ZmSNAC052 N/A Drought, cold U Lu et al. (2015)
Zma029150 N/A Drought, salt U Lu et al. (2015)
WRKY ZmWRKY17 (W-box) TTGACC/T Drought, salt, ABA bHLH92, KIN1, DREB1F, etc Cai et al. (2017)
ZmWRKY33 (W-box) TTGACC/T High salinity, dehydration, cold, ABA RD29A and DREB1B Li et al. (2013)
ZmWRKY44 (W-box) TTGACC/T Salt, high temperature, ABA, H2O2 U Wang (2014)
ZmWRKY58 (W-box) TTGACC/T Drought, ABA, salt U Cai et al. (2014)
ZmWRKY106 (W-box) TTGACC/T Drought, high temperature, ABA, salt CuZnSOD, DREB2A, NCED6, and RD29A Wang et al. (2018c)
ZmWRKY40 (W-box) TTGACC/T Drought, high salinity, high temperature, ABA DREB2B, STZ, and RD29A Wang et al. (2018a)
HD-Zip Zmhdz10 CAATAATTG Salt, ABA ABI1, RD22, P5CS1, etc Zhao et al. (2018)
ZmHDZ4 CAATAATTG Drought U Wu et al. (2016)
HSP ZmERD2 N/A Heat, salinity, cold, PEG, dehydration U Song et al. (2016)
NF-Y ZmNF-YB16 CCAAT Dehydration, Drought P5CS, Atj3, AtDJC82, HSP70, etc Wang et al. (2018b)
ZmNF-YB2 CCAAT Drought U Nelson et al. (2007)
ZmNF-YA3 CCAAT Drought, high temperature ZmbHLH92, ZmMYC4, and ZmFAMA Su et al. (2018)
DOI: 10.7717/peerj.7211/table-1


Abiotic stress-related TF families, together with the specific TFs, their characteristics, the regulons they control and their regulatory functions in the abiotic stress responses in Maize.

N/A-The cis-acting element is unknown, U-unknown.

Another maize MYB TF, ZmMYB31 was found to repress the biosynthesis of sinopoylmalate leading to increased sensitivity to UV irradiation and dwarfism in transgenic plants (Fornalé et al., 2010). Furthermore, ZmMYB31 activated a number of stress-responsive genes (ZmF5H, C3H, ZmActin, and ZmCOMT) in vivo in maize, and 4CL1 and COMT genes in transgenic Arabidopsis. The roles of maize MYB related genes in response to drought stress were examined based on microarray data (Dash et al., 2012; Du et al., 2013). On the maize 18k GeneChip, 26 probe sets were shown to correspond to 32 MYB-related genes (whereby five probes represented one gene). Further analysis of this highly similar sequence data revealed that the majority of the MYB-related genes were expressed at low levels, although their expression was in response to a specific stress. Elsewhere, gene expression analysis between two maize varieties, a drought sensitive (Ye478) variety, and a drought tolerant (Han21) variety was found to be very similar (Du et al., 2013). For instance, four CCA1-like/R–R genes (ZmMYBR49, ZmMYBR19, ZmMYBR56, and ZmMYBR28), six TBP-like genes (ZmMYBR55, ZmMYBR45, ZmMYBR47, ZmMYBR31, ZmMYBR26, and ZmMYBR07) and a single TRF-like gene (ZmMYBR41) were all elevated in response to drought stress. Expression analysis of ZmMYBR37 an I-box-like gene, and five CCA1-like/R–R genes (ZmMYBR63, ZmMYBR44, ZmMYBR27, ZmMYBR18, and ZmMYBR03), showed that these genes were highly down-regulated in response to drought stress. Although recovery of all these genes above was observed after re-watering (Table 1). Similarly, a maize R1-type TF that is encoded by ZmMYB-R1 gene was activated by cold, exogenous ABA, drought, heat and high salinity (Liu et al., 2012). Functional analysis of ZmMYB-R1 in different tissues revealed it first reached its maximum levels in the leaves and later it was detected in the roots and stems.

In the model plant Arabidopsis, MYB and MYC TFs were found to accumulate in plant tissues following the accumulation of ABA (Lata, Yadav & Prasad, 2007). Seven Arabidopsis MYB TF genes namely AtMYBCDC5, AtMYB77, AtMYB73, AtMYB44, AtMYB6, AtMYB7, and AtMYB4 were all strongly expressed in all organs, in response to several abiotic stresses (Yanhui et al., 2006). Functional analysis of two MYB/MYC genes (AtMYC2 and AtMYB2), in transgenic Arabidopsis revealed that the TF proteins encoded by these two genes can bind to the promoter regions of several ABA or JA inducible genes. For example, AtADH1 and RD22 thus making the transgenic Arabidopsis plants ABA-responsive and more tolerant to both drought and osmotic stress (Abe et al., 2003).

Taken together, all the above findings suggest that MYB genes could be engineered in crops leading to activation of general pathways involved in abiotic stress responses in plants. For instance, overexpression of OsMYB55, a rice R2R3-MYB TF significantly improved rice plants tolerance to extreme temperatures, and this was directly linked with improved amino acid metabolism (El-kereamy et al., 2012). Additionally, these findings will facilitate our understanding of gene regulation by MYB TFs, thus leading to the development of new abiotic stress tolerant crop varieties. Finally, phylogenetic, functional, and structural analyses revealed that most homologous MYB proteins that possess conserved domains have similar activities and functions in divergent plant species. Although a lot of information is available on the molecular functioning of MYB TFs in abiotic stress responses, deciphering the downstream and upstream events in MYB TFs in abiotic stress responses remains an immense undertaking.

The AP2/EREBP regulons

The AP2/EREBP (ET-responsive element binding protein) family is made up of a large group of plant specific TFs that are characterized by the presence of a highly conserved AP2/ET-responsive element binding factor (ERF). The ERF interacts directly with GCC box and/or DRE/C-repeat element (CRT) at the promoter site of downstream target genes (Riechmann & Meyerowitz, 1998). AP2/EREBP TFs play vital roles in stress responses and developmental processes such as cell proliferation, plant hormone responses, and biotic and abiotic stress responses (Sharoni et al., 2011). Based on the similarity and number of AP2/ERF domains, AP2/EREBP TFs are grouped into four main subfamilies: ERF, RAV (related to AB13/VP1), DREB and AP2 (Apetala 2) (Sharoni et al., 2011). Among these four, the DREB subfamily has been extensively studied due to the roles its TFs play in plant biotic and abiotic stress responses.

Dehydration responsive element binding proteins play a significant role in the ABA-independent pathways that are responsible for the activation of abiotic stress-regulatory genes (Lata, Yadav & Prasad, 2007). DREB TFs are made up of one AP2/ERF DNA binding region, which binds to the cis-acting element DRE composed of TACGACAT (a nine bp core sequence) and is present in the promoters of abiotic stress-responsive genes (Gahlaut et al., 2016). The existence of this cis-acting element (CRE) has been recorded in several abiotic stress-responsive genes, for example, RD29B and RD29A in Arabidopsis (Yamaguchi-Shinozaki & Shinozaki, 1994). CRT cis-acting element consisting of the A/GCCGAC motif and which are similar to DREBs, have been identified in the promoter regions of cold-responsive genes in Arabidopsis, whereby the CRT elements bind to the TF CBF (CRT binding factor) in response to cold stress (Saleh, Lumreras & Pages, 2005). In Arabidopsis, for example, exogenous overexpression of AtDREB1/CBF led to cold, drought, and high salinity tolerance in transgenic plants. These findings clearly suggest that DREBs/CBFs TFs have the potential to target multiple stress-responsive candidate genes in the plant genomes (Jaglo-Ottosen et al., 1998; Kasuga et al., 1999).

In maize, the role of DREB TFs has been investigated by adopting both molecular and genetic analyses (Zhuang et al., 2010). For example, ZmDREB1A was activated by cold stress and moderately elevated by high-salinity stress in maize seedlings (Qin et al., 2004) (Table 1). Overexpression of ZmDREB1A in transgenic Arabidopsis led to induced overexpression of abiotic stress-activated genes giving rise to plants with enhanced tolerance to extreme drought and freezing stresses (Table 2). Investigations were done to ascertain whether ZmDREB1A could induce other genes in the dehydration and/or cold pathways of wild-type plants. The results revealed that expression levels of KIN1, KIN2, and COR15A were all highly up-regulated in the 35S:ZmDREB1Aa transgenic line under normal conditions when compared to the wild-type plants. Expression analysis of RD17, ERD10, and RD29A showed that these genes were slightly up-regulated in the 35S:ZmDREB1Aa transgenic line. The above results showed that ZmDREB1A induces both ABA-independent genes like COR15A, KIN1, and KIN2 and ABA-dependent genes like RD17, ERD10, and RD29A. Therefore, it was concluded that this gene might affect the expression of dehydration and cold-responsive genes in both the ABA-independent and ABA-dependent pathways. Likewise, another DREB TF gene ZmDBP3 was highly induced by cold and moderately induced by salinity stress (Wang & Dong, 2009) (Table 1). Overexpression of this gene in transgenic Arabidopsis led to improved tolerance to both cold and drought stresses (Chang & Yin, 2009) (Table 2).

Table 2:
Abiotic stress responses of overexpressing Maize TFs in transgenic plants.
Family Gene Stress tolerance Transgenic plant References
MYB/MYC ZmMYB30 Salt Arabidopsis Chen et al. (2017)
ZmMYB31 Sensitivity to UV irradiation Arabidopsis Fornalé et al. (2010)
DREB/CBF ZmDREB2A Drought, heat Arabidopsis Qin et al. (2007)
ZmDBP3 Cold, salt Arabidopsis Wang & Dong (2009) and Chang & Yin (2009)
ZmDBF3 Salt, freezing Yeast (Saccharomyces cerevisiae) Zhou et al. (2016)
ZmDREB1A Drought, Freezing Arabidopsis Qin et al. (2004)
ZmDREB2.7 Drought Arabidopsis Liu et al. (2013)
ZmDBP4 Drought, cold Arabidopsis Wang, Yang & Yang (2011)
bZIP ZmbZIP60 Dithiothreitol (DDT) Arabidopsis Wang et al. (2012)
ZmbZIP72 Drought, partial salinity Arabidopsis Ying et al. (2012)
Abp9 Salt, osmotic stress Cotton (Gossypium hirsutum) Wang et al. (2017)
Drought, ABA, salt Arabidopsis Zhang et al. (2011)
NAC ZmSNAC1 Sensitivity to ABA, osmotic stress Arabidopsis Lu et al. (2012)
Tolerance to dehydration
ZmNAC55 Sensitivity to ABA Arabidopsis Mao et al. (2016)
Tolerance to drought
ZmNAC111 Drought Maize (Zea mays) Mao et al. (2015)
WRKY ZmWRKY17 Sensitivity to salt Arabidopsis Cai et al. (2017)
Tolerance to ABA
ZmWRKY33 Salt Arabidopsis Li et al. (2013)
ZmWRKY44 Sensitivity to salt Arabidopsis Wang (2014)
ZmWRKY58 Enhanced tolerance to drought, salt Rice (Oryza sativa) Cai et al. (2014)
ZmWRKY106 Drought, heat stress Arabidopsis Wang et al. (2018c)
ZmWRKY40 drought Arabidopsis Wang et al. (2018a)
HSF ZmHsf06 Drought, thermotolerance Arabidopsis Li et al. (2015)
HD-Zip Zmhdz10 Drought, salt sensitivity to ABA Rice (Oryza sativa) Zhao et al. (2018)
Drought, salt Arabidopsis
ZmHDZ4 Drought Rice (Oryza sativa) Wu et al. (2016)
Zmhdz12 Drought Arabidopsis Qing & Wei (2018)
NF-Y ZmNF-YB2 Drought Maize (Zea mays) Nelson et al. (2007)
ZmNF-YB16 Drought, dehydration Maize (Zea mays) Wang et al. (2018b)
DOI: 10.7717/peerj.7211/table-2


Represents the abiotic stress responses of overexpressing Maize TFs in transgenic plants.

Natural variations present in the promoter region of another maize DREB TF gene ZmDREB2, lead to drought tolerance in maize (Liu et al., 2013) (Table 1). In transgenic Arabidopsis, overexpression of ZmDREB2 resulted in plants with enhanced tolerance to drought. Elsewhere, qRT-PCR analysis of maize leaves revealed that expression of ZmDREB2A was induced by dehydration, heat and cold stress (Qin et al., 2007). Overexpression of ZmDREB2A in transgenic Arabidopsis resulted in dwarf plants with enhanced tolerance to drought and heat stresses. Microarray analysis of these transgenic Arabidopsis plants identified a number of genes associated with detoxification and heat shock (HS) for example RD29B and At5G03720. Moreover, five genes coding for LEA proteins (LEA14, At1g52690, At3G53040, At3G15670, and At2G36640) in addition to a metabolism associated gene AtGoIS3, were all up-regulated under different stress treatments in the transgenic lines (Table 1). Elsewhere, functional analysis of ZmDBF3 showed that this TF gene was activated by drought, high temperature, salt, cold, and ABA. However, no significant difference was noted under methyl jasmonate and SA (Zhou et al., 2016). Ectopic expression of ZmDBF3 in yeast (Saccharomyces cerevisiae) resulted in a higher survival rate during exposure to KCI, Na2CO3, NaHCO3, NaCl, PEG 6000, sorbitol, and freezing temperatures. Moreover, exogenous expression of ZmDBF3 in transgenic Arabidopsis considerably improved tolerance to drought, freezing, and salt stresses (Table 2). These findings, suggest that ZmDBF3, a novel maize DREB TF may have similar functions to a regulatory factor taking part in abiotic stress response pathways. Similarly, overexpression of ZmDBP4 in Arabidopsis resulted in transgenic plants with improved cold and drought stress tolerance (Wang, Yang & Yang, 2011) (Table 2). Analysis of the promoter region of ZmDBP4 identified cis-acting elements which responded to abiotic stresses, suggesting that ZmDBP4 encodes a functional factor that plays an important role in the control of multiple abiotic stress responses in maize. Elsewhere, mRNA accumulation analysis profiles of two DRE-binding proteins (DBF1 and DBF2) in maize seedlings revealed that DBF1 was induced during embryogenesis and in response to drought, ABA, and NaCl treatments (Kizis & Pages, 2002).

Dehydration responsive element binding TFs are versatile when it comes to abiotic stress regulation. Recently, numerous studies have been done to understand the roles DREB TFs play in abiotic stress responses and to reveal the mechanisms involved in their transcription and post transcriptional regulation. Collectively, these studies suggest that DREB TFs can be potential candidates for abiotic stress tolerance, although these studies have not addressed the vital question of whether DREB TFs can improve the yield of engineered crops under stress. Many DREB homologues have been identified and isolated from different plant species, especially from plant species with exceptional tolerance to different abiotic stresses. Thus, the focus now is to evaluate the existing methods of yield analyses under different stress conditions and to assess transgenic plants in actual field conditions.

NAC TFs and regulons

The TF members in the NAC family, (ATAF, CUC, and NAM) represent one of the largest plant-specific TFs (Ooka et al., 2003). In the main crop species, a large number of NAC TFs have been analyzed and sequenced at the genome-wide level. These include 151 members in rice and 117 in Arabidopsis (Nuruzzaman et al., 2010), 204 members in the Chinese cabbage (Liu et al., 2014b), and 152 members in maize (Shiriga et al., 2014). The TFs belonging to the NAC family share a greatly conserved N-terminus made up of 150–160 amino acid residues, constituting a DNA-DB that carries five sub-domains (A–E) and a varying C-terminal (Hu et al., 2008; Ooka et al., 2003). The NAC genes and their constituent cis-acting elements make up the NAC regulons, which further provide vital examples of finely characterized collaboration between a single TF and one or more cis-acting elements that associate in response to multiple stresses (Christianson et al., 2010). The roles of NAC TFs in plants have been extensively studied in rice and Arabidopsis. In Arabidopsis, for example, an ERD1 (early dehydration stress 1) gene was activated by a number of NAC TFs including ANAC055, ANAC019, and ANAC072 (Tran et al., 2007). A rice NAC TF designated as OsNAM, was found to regulate the activation of five genes (OsAH, OsCESA, OsMtN3, OsGdpD, and OsGDP) in response to drought (Dixit et al., 2015). Several NAC TFs utilize the NACRS motif in plants, for instance SNAC2 and ENAC1 found in rice (Sun et al., 2012) and ANAC055, ANAC072, and ANAC019 found in Arabidopsis (Tran et al., 2004).

In maize, several NAC TFs involved in abiotic stress regulatory pathways have been isolated, cloned, and characterized. Recently, expression analysis of ZmSNAC1 in maize seedlings revealed that this TF gene was strongly induced by high salinity, drought, ABA treatment, and low temperature, although it was down-regulated in response to SA treatment (Lu et al., 2012). Overexpression of ZmSNAC1 in transgenic Arabidopsis led to increased hypersensitivity to osmotic stress and ABA as well as enhanced tolerance to dehydration stress at the germination phase (Table 2). These results suggest that ZmSNAC1 acts as a multiple stress responsive TF, positively modulating abiotic stress tolerance in maize. Elsewhere, Shiriga et al. (2014) identified 11 NAC TF genes in maize that were induced by various abiotic stresses. This prediction was confirmed when these genes were differentially expressed in response to drought stress. Four genes, ZmNAC45, ZmNAC72, ZmNAC18, and ZmNAC51 were all up regulated in the drought-tolerant maize genotypes and down-regulated in the drought susceptible genotypes. Recently, seven ZmNTL, NAC TFs genes (ZmNTL1, ZmNTL2, ZmNTL3, ZmNTL4, ZmNTL5, ZmNTL6, and ZmNTL7) were analyzed in maize seedlings and all seven genes were found to be strongly expressed in the stem and roots and down-regulated in the leaves when the plants were exposed to H2O2 and/or ABA treatments. Exogenous expression of ZmNTL1, ZmNTL2, and ZmNTL5 in transgenic Arabidopsis led to increased tolerance to H2O2 in transgenic plants (Wang et al., 2016a). Overexpression of ZmNAC55 in transgenic Arabidopsis resulted in plants which were hypersensitive to ABA at the seedling stage but showed enhanced resistance to drought when compared to the wild-type control seedlings (Mao et al., 2016). Additionally, 12 stress-responsive genes (RD20, NCED3, ZAT10, ANAC019, LEA14, RD29B, RD29A, DREB2A, RD17, RD26, RAB18, and PP2CA) were all up regulated in response to drought stress in the transgenic lines (Table 1). Expression profiles of ZmNAC55 in maize revealed that this gene was induced by high salinity, drought, ABA, and cold stress.

Elsewhere, seven NAC TF genes analyzed in maize seedlings (Zma001259, Zma000584, Zma029150, ZmSNAC052, Zma003086, Zma054594, and Zma006493) were all found to be up regulated in response to salt stress in all tissues (Lu et al., 2015). In response to PEG treatment, three of the above-mentioned genes, namely Zma006493, Zma003086, and Zma000584 were significantly up regulated in the roots only, while Zma001259, Zma029150, Zma000584, and Zma054594 were all strongly expressed in both the roots and shoots. Five genes, Zma054594, Zma000584, Zma001259, Zma003086, and ZmSNAC052 were activated by cold stress although in varying degrees. In conclusion, due to the strong expression in response to ABA treatments, these seven genes could play a vital role in the ABA-dependent signaling network in maize.

Numerous advancements in NAC TFs functional studies have been achieved over the past few years. However, most of these studies are related to the involvement of NAC TFs in biotic stress responses. To achieve a deeper understanding of NAC TFs in abiotic stress responses, it is of vital importance to identify the main components of signal transduction pathways that interact with these TFs. Utilizing data obtained from microarray analyses could help in the direct determination of specific NAC DNA-binding sites on a global scale under different abiotic stress conditions.

Finally, numerous studies have demonstrated the use of stress-responsive NAC TFs in the improvement of abiotic stress tolerance in crops by genetic engineering. In view of the specificity of NAC TF in multiple stress responses, NAC TFs that are induced by multiple abiotic stresses are promising candidates in the engineering of plant varieties with improved multiple stress tolerance (Shao, Wang & Tang, 2015). Moreover, field evaluation of engineered crops containing NAC TF genes and efficient promoters, for reducing detrimental effects triggered by overexpression of some NAC genes must be considered (Rushton et al., 2008).

bZIP TFs: AREB/ABF regulon

The ABRE (PyACGTGG/TC), is a conserved cis-acting element bound by the basic Leucine Zipper Domain (bZIP) TFs (Ciarmiello et al., 2011). The ABRE was first established on the promoter region of ABA-activated genes by Giraudat et al. (1994). The bZIP TFs belong to one of the largest and diversified TF families in plants. They are categorized into ten subfamilies based on the presence of extra conserved motifs and the basic region sequence similarities (Pérez-Rodríguez et al., 2010). AREB/ABF TFs are characterized by a strongly conserved bZIP domain made up of two structural components (a leucine (Leu) zipper and a basic region), the Leu zipper is composed of heptad repeats of Leu and/or other heavy hydrophobic amino acid residues and controls hetero- and or homodimerization of the bZIP proteins. The basic region is composed of 16 amino acids with the indistinguishable N-x7-R/K-x9 motif and is responsible for DNA binding and nuclear localization (Jakoby et al., 2002). The bZIP TFs, which are part of the AREB/ABF regulons, give an excellent example of interactions involving stress-responsive genes and TFs carrying the cis-acting element (ABRE). In maize, a bZIP TF gene ABP9 that has the ability to bind to the AREB2 motif located in the Cat1 promoter region was activated by drought, salt, H2O2, and ABA (Zhang et al., 2011). Exogenous expression of ABP9 in Arabidopsis led to significant tolerance to freezing, salt, oxidative stress, and drought in transgenic plants. Transgenic Arabidopsis plants also showed enhanced sensitivity to exogenously supplied ABA during stomatal closure, seed germination, and root growth. Furthermore, transgenic plants expressing ABP9 showed reduced levels of oxidative cellular damage, reduced cell death, and reduced levels of ROS.

More recently, Wang et al. (2017) demonstrated that ABP9 enhanced salt and osmotic stress tolerance in transgenic cotton plants. Overexpression of ABP9 resulted in elevated transcripts of several stress responsive-genes (GhNCED2, GhDBP2, GhZFP1, GhHB1, GhSAP1, and GhERF1) in the transgenic cotton plants in response to salt stress (Table 2). Additionally, transgenic plants were shown to have higher germination rates, and improved root systems in a greenhouse setting and reduced stomatal density and stomatal aperture in a growth room. Finally, the relative water content and survival rate of the transgenic plants was significantly higher compared to the control plants in response to drought. Wang et al. (2012) demonstrated that expression of ZmbZIP60 was highly activated by a wide range of stresses including ABA, high salinity, tunicamycin treatment, and dehydration (Table 1). In the wild-type Arabidopsis, overexpression of ZmbZIP60 resulted in plants with enhanced tolerance to dithiothreitol stress. Furthermore, Li et al. (2018) discovered a major QTL governing heat-induced ZmbZIP60 expression and deduced that the upstream region of ZmbZIP60 plays a vital role in regulating responses to heat stress in maize.

Similarly, Ying et al. (2012) cloned and characterized a maize bZIP TF gene designated as ZmbZIP72, which was induced by drought, ABA, and high salinity stress (Table 1). ZmbZIP72 was differentially expressed in various organs in maize. Overexpression of ZmbZIP72 in transgenic Arabidopsis led to enhanced tolerance to drought, partial tolerance to salinity and hypersensitivity to osmotic stress and ABA treatment. Furthermore, the transgenic Arabidopsis plants also showed enhanced expression of several ABA-inducible genes including (RAB18, HIS1-3, and RD29B). Elsewhere, microarray analysis of two specific maize inbred lines, a drought-sensitive Ye478 line, and a drought tolerant Han21 line revealed that 22 ZmbZIP genes might play a critical role in drought tolerance (Wei et al., 2012a). In the same report, ZmbZIP37 an orthologous gene of two rice genes OsbZIP72 and OsbZIP23 that both play vital roles in drought tolerance and ABA response in rice, was found to be up-regulated in response to drought stress in maize. Similarly, cloning and characterization of a bZIP TF gene ZmbZIP17 from the Han21 maize inbred line revealed that this gene was up regulated in response to drought (Jia et al., 2009). Real-time PCR analysis revealed that ZmbZIP17 was highly up regulated in response to heat, salinity, drought, and ABA stresses immediately, suggesting that this gene represents an early responsive gene that reacts to various abiotic stresses. Elsewhere, expression analysis of two maize bZIP TF genes ZmbZIP107 and ZmbZIP54 revealed that these two genes were highly elevated in a lead tolerant maize line when compared to a lead sensitive line in response to different treatments of lead (Zhang et al., 2017a) (Table 1). Recently, Ma et al. (2018) demonstrated that ZmbZIP4 was induced by drought, cold, high salinity, ABA, and heat in maize seedlings. Overexpression of ZmbZIP4 led to an improved root system, increase in the number of lateral roots, and longer primary roots in transgenic maize. Additionally, genome-wide analysis of ZmbZIP4 target genes by immunoprecipitation sequencing, unearthed a number of downstream stress response genes that were positively regulated by ZmbZIP4. These downstream target genes included ZmRD21, ZmLEA2, ZmRD20, ZmGEA6, ZmNHX3, and ZmRAB18. Collectively, these results suggested that ZmbZIP4 is a positive regulator of abiotic stress response that takes part in root development in maize.

In conclusion, the promoter region of each abiotic stress responsive gene might carry a single or several proximal or distal coupling elements (CE) for instance, CE 3 and CE1 which activate the expression of abiotic stress-responsive genes. In addition, Shen, Zhang & Ho (1996) identified CEs in Hordeum vulgare that form an abscisic acid response complex, which could be a necessary component in triggering ABA-mediated gene expression. Collectively, the above reports confirmed the participation of bZIP TFs in the ABA signaling pathway. These findings could be useful in the future development of better genotypes with improved tolerance to various abiotic stresses (Todaka, Shinozaki & Yamaguchi-Shinozaki, 2015). An accurate understanding of the functions of bZIP TFs in crops will require an accurate mapping of the location of bZIP genes in the different plant organs.

WRKY TFs and WRKY regulons

WRKY proteins represent the largest superfamily of TFs, which are specific to plants. WRKY TFs control plant growth and development and spur tolerance against both abiotic and biotic stresses (Tripathi, Rabara & Rushton, 2014). WRKY TFs are usually identified by a WRKY domain made up of 60 amino acid residues, and contains a highly conserved WRKYGQK sequence followed-up by a zinc-finger motif. The WRKY domain shows a strong binding affinity for a cis-acting element known as W-box (TTGACC/T), which is present in a number of abiotic stress responsive genes (Rushton et al., 2010; Ulker & Somssich, 2004).

Several WRKY TFs involved in abiotic stress tolerance have recently been reported in maize. For example, functional analysis of ZmWRKY33 under different abiotic stresses, revealed that this gene was activated by cold, dehydration, ABA, and salt treatments (Li et al., 2013). Overexpression of ZmWRKY33 in transgenic Arabidopsis led to the activation of two stress-activated genes (RD29A and DREB1B), which were both up-regulated resulting in enhanced salt tolerance in the transgenic plants (Table 1). The above-mentioned results strongly suggest that this maize WRKY TF plays a vital role in abiotic stress regulation in maize. Elsewhere, Wang (2014) demonstrated that exogenous overexpression of ZmWRKY44 in transgenic Arabidopsis resulted in plants that were moderately sensitive to NaCl stress. In maize seedlings, ZmWRKY44 was induced by high temperature, salt stress, ABA, and H2O2 treatments. Recently, ZmWRKY17 was cloned, characterized and its expression was analyzed in maize seedlings (Cai et al., 2017) (Table 1). The results showed ZmWRKY17 was induced by ABA, salt, and drought stresses. Additionally, constitutive expression of this gene in transgenic Arabidopsis led to a striking reduction in tolerance to salt stress, as confirmed by the physiological assays performed on relative electrical leakage, MDA content, cotyledons greening rate and root growth. Still in the same study, RNA-Seq analysis showed that eight stress-related genes (DREB1F, KIN1, bHLH92, RD29A, RD29B, NAC019, RD22, and MYB101) were significantly up-regulated in the wild-type plants when compared to the transgenic plant lines in response to salt stress. However, expression of NCED5 was higher in transgenic plants under the same stress. Together, these results give a strong indication that ZmWRKY17 may function as a negative regulator in response to drought stress in maize. This could be due to elevated levels of ABA ensuing as a direct response to salt stress through the ABA signaling system. Wei et al. (2012b) compared the expression profiles of 31 WRKY genes in two maize lines, a drought-sensitive Ye478 line and a drought tolerant Han21 line. The results showed that the expression of the WRKY genes in the drought-tolerant Han21 line changed less, and the seedlings recovered faster when re-watered, as opposed to the drought-sensitive Ye478 seedlings. In the same study, the expression of ZmWRKY115 was decreased as a direct result of drought stress. Elsewhere, qRT-PCR expression analysis showed that ZmWRKY58 was activated by salt, drought and ABA treatments (Cai et al., 2014) (Table 1). Constitutive expression of ZmWRKY58 in transgenic rice led to delayed germination and constrained post-germination growth and development. However, transgenic seedlings overexpressing ZmWRKY58 reported increased tolerance to both salt and drought stresses (Table 2). Similarly, Wang et al. (2018a) identified a WRKY TF gene named ZmWRKY40 (Table 1). A number of stress-related transcriptional regulatory factors were located in the promoter region of this gene. In maize, ZmWRKY40 was induced by high salinity, drought, ABA, and high temperature. Overexpression of ZmWRKY40 in Arabidopsis led to enhanced drought tolerance in the transgenic plants. Additionally, overexpression of ZmWRKY40 induced the expression of three stress-responsive genes DREB2A, STZ, and RD29A in transgenic Arabidopsis. Recently, the expression of ZmWRKY106, a member of the WRKYII group was found to be induced by high temperature, drought, and exogenous ABA treatment, but was weakly induced by salinity (Wang et al., 2018c). Overexpression of ZmWRKY106 in transgenic Arabidopsis led to improved tolerance to heat and drought. Additionally, ZmWRKY106 positively regulated the expression of several stress response genes including RD29A, CuZnSOD, DREB2A, and NCED6. The above results strongly indicate ZmWRKY106 may play an important role in the abiotic stress response pathways in maize by regulating stress-related genes.

In the model plant Arabidopsis, two WRKY genes WRKY 60 and WRKY 18 were found to regulate ABA signaling positively while one WRKY gene WRKY40 negatively regulated ABA signaling. These three WRKY genes mentioned above, bind to the promoter region of several genes including some TFs genes like (DREB1A/CBF3, ABI5, and DREB2A), and several stress-regulated genes like (COR47 and RD29A) in the process controlling their expression (Shang et al., 2010; Chen et al., 2010).

WRKY TFs have been identified as promising candidates for crop improvement due to the strict regulations involved in the identification and binding of these TFs to the downstream target promoter regions (Phukan, Jeena & Shukla, 2016). Taken together, all the above insights highlight the multiple stress responses and diverse regulation of WRKY TFs in maize and other crops.

Other TFs and their regulons

Apart from the five main TF families described above, other TF families take part in diverse roles in plants including, regulating responses to both abiotic and biotic stresses, and various growth and development processes. Recently, extensive research has uncovered stress-mitigating roles of a number of TFs whose responses to abiotic stressors were previously unknown in maize. Three of these TF families are briefly described below.

Homeodomain-leucine zipper I

Homeodomain-leucine zipper (HD-Zip) proteins represent a large TF family that is specific to plants. HD-Zip proteins have been cloned and characterized in several important crops and some model plants such as rice, Arabidopsis, tomato, and sunflower (Johannesson et al., 2003; Lin et al., 2008; Agalou et al., 2008; Manavella et al., 2006). HD-Zip proteins are characterized by a DNA-binding HD and a neighboring leucine zipper (Zip) motif whose function is to mediate protein dimerization (Ariel et al., 2007). HD-Zip proteins belonging to the subfamily I are believed to take part in the majority of plant responses to abiotic stresses (Ariel et al., 2007). In Arabidopsis for example, analysis of four HD-Zip TFs (ATHB6, ATHB7, ATHB5, and ATHB12) revealed that these genes were up-regulated or repressed by either ABA or drought stress (Soderman, Mattsson & Engstrom, 1996; Soderman et al., 1999; Lee et al., 2001; Johannesson et al., 2003). These results suggest that these four genes may play a vital role in the regulation of abiotic stress regulatory networks in plants.

In maize, Zmhdz10 was the first HD-Zip TF to be isolated and characterized (Zhao et al., 2014). Expression of this gene was activated by ABA treatment and salinity stress (Table 1). Exogenous overexpression of Zmhdz10 in transgenic rice resulted in improved tolerance to salt and drought stress and enhanced sensitivity to ABA. Furthermore, the transgenic plants had elevated levels of proline and reduced MDA content when compared to the wild-type plants (Table 2). Transgenic Arabidopsis plants overexpressing Zmhdz10 exhibited strong tolerance to salt and drought stresses, at the same time, expression patterns of several ABA-responsive genes namely (ABI1, RD29B, P5CS1, and RD22) were altered. The above results give a strong indication that Zmhdz10 serves as a transcriptional regulator that can positively regulate both salt and drought stress tolerance in the ABA-dependent pathway in plants. Recently, Qing & Wei (2018) isolated and characterized a maize HD-ZIP TF designated as Zmhdz12. Tissue expression analysis revealed that this TF was strongly expressed in the leaves compared to other tissues. In transgenic Arabidopsis, Zmhdz12 was activated by drought as observed when the drought resistant transgenic lines were compared to the wild-type lines. Similarly, expression status of 17 Zmhdz I genes from maize (Zmhdz1 to Zmhdz17) revealed that all these genes were either repressed or up-regulated due to drought stress (Zhao et al., 2011). Additionally, many of the genes above belonging to the same subgroup in the phylogenetic tree, showed similar patterns of expressions. Elsewhere, ZmHDZ4 was isolated and characterized in maize for its role in drought stress tolerance (Wu et al., 2016). Overexpression of ZmHDZ4 in transgenic rice resulted in plants with enhanced tolerance to drought.

In conclusion, it is worth noting that HD-Zip proteins play crucial roles in cuticle formation, so they might be involved in abiotic stress tolerance and protection against plant pathogens (Chew, Hrmova & Lopato, 2013). In addition, the roles described above make HD-Zip TFs ideal candidates for genetic engineering in maize and other major crops. Although more in-depth studies are needed in order to ascertain the function of individual HD-Zip family members in response to various abiotic stresses.

Heat shock proteins

All organisms are composed of an evolutionarily conserved, fast cellular defense system known as HS response, which regulates various reactions associated with heat stress and a variety of chemical stressors (Lin et al., 2011). Heat shock proteins (HSPs) were first discovered in the salivary glands of Drosophila in response to HS (Ashburner & Bonner, 1979). HSFs family members function by binding to the promoter of chaperones referred to as HSPs. HSF TFs have a three N-terminal section and a C-terminal section in addition to leucine amino acid (Schuetz et al., 1991). HSPs can be categorized into six main families, (Hsp90, Hsp40, Hsp90, Hsp60, Hsp70, and Hsp110) based on their molecular sizes (Wang et al., 2004). HSPs in plants were first characterized in tomato (Scharf et al., 1990), and since then more HSFs have been reported in other plants such as Arabidopsis, rice, sunflower, and wheat (Hübel & Schöffl, 1994; Yamanouchi et al., 2002; Almoguera et al., 2002; Shim et al., 2009). A survey recently reported that there are at least 24 HSFs in Brachypodium, 21 in Arabidopsis, 30 in maize, 25 in rice, 52 in soybeans, and 27 in tomatoes (Scharf et al., 2012). In the model plant Arabidopsis, a HsfA2 mutant displayed tolerance to osmotic stress, salt, and heat stresses, suggesting that this gene is involved in several abiotic stress response networks and pathways (Ogawa, Yamaguchi & Nishiuchi, 2007).

Few HSPs gene have been isolated and characterized in maize. Song et al. (2016) isolated and characterized a Hsp70 gene named ZmERD2 (Early Responsive to Dehydration 2) from maize (Table 1). Expression patterns of ZmERD2 revealed that this gene was induced by cold, high salinity, dehydration, heat stress, and PEG but was not induced by ABA. Further expression analysis revealed ZmERD2 was instantly activated at 42 °C and its peak was reached after 1 h of exposure to heat stress. Elsewhere, expression patterns of 22 Hsf genes from maize showed that these genes were differentially expressed when subjected to heat stress (Lin et al., 2011). Further analyses from this study revealed that ZmHsfA2 subclass in maize has close relations with HS response. This is after three HsfA2 genes (ZmHsf-17, ZmHsf-01, and ZmHsf-04) were strongly expressed in response to heat stress. In addition, six more genes were highly up-regulated in response to heat stress (ZmHsf-03, ZmHsf-01, ZmHsf-23, ZmHsf-24, ZmHsf-04, and ZmHsf-25). These results pointing to the specific roles these genes play in maize in response to heat stress. Li et al. (2015) recently cloned a maize HSF designated as ZmHsf06 from maize and transformed it in Arabidopsis thaliana. Expression analysis of the transgenic plants overexpressing ZmHsf06 revealed that this gene was induced by drought and heat stress (Table 2). The above results were confirmed by biochemical and physiological evidence that showed that the transgenic plants displayed longer axial root length, higher seed germination rate, elevated levels of chlorophyll in leaves as well as reduced osmotic potential and MDA content when compared to the wild-type plants. Based on the above results, it’s evident ZmHsf06 could have future potential use in molecular breeding in maize as well as other crops for improved drought and heat stress tolerance.

Collectively, it is important to mention that HSPs have been shown to have a close association with ROS, meaning that plants have gained a stronger level of ROS regulation throughout the course of evolution (Banti et al., 2010). Therefore, understanding the roles played by HSPs in plant responses to abiotic stresses will be useful in the engineering of abiotic stress tolerant crop varieties. HSP have been studied and characterized in a number of important crop varieties as mentioned above, although their functional plasticity, and genome sequence data is still limited (Echevarría-Zomeño et al., 2016).

NF-Y transcription factors

Nuclear factor Y also referred to as CBF (CCAAT binding factor) or heme activator protein (HAP), is a complex made up of three subunits NF-YB (CBF-A or HAP3), NF-YA (CBF-B or HAP2) and NF-YC (CBF-C or HAP5) (Nardini et al., 2013; Wang et al., 2018b). The NF-Y TF family has been comprehensively studied in animal systems, and it was found that each subunit is encoded by a single gene in yeast and mammals (Mantovani, 1999). NF-Y TFs interact with other factors in the regulatory network to induce or inhibit the expression of downstream target genes (Benatti et al., 2008). Unlike mammals and yeast, plants have many NF-Y subunit genes (Wang et al., 2018b). For example, in Arabidopsis 13 genes encoding NF-YB, 10 genes encoding NF-YA, and 13 genes encoding NF-YC have been reported (Siefers et al., 2009). Additionally, individual NF-Y subunits have been shown to play vital roles in plant abiotic stress tolerance (Sato et al., 2014; Ma et al., 2015).

Even though maize has numerous NF-Y subunits, very few studies have been done to investigate the roles these subunits play in response to abiotic stress (Wang et al., 2018b). Nelson et al. (2007) demonstrated that transgenic maize with elevated levels of ZmNF-YB2 showed improved tolerance to drought stress based on responses from various stress-related parameters which included stomatal conductance, chlorophyll content, reduced wilting, and leaf temperature (Table 2). Recently, overexpression of a NF-YB TF complex member designated as ZmNF-YB16 resulted in improved drought and dehydration resistance in transgenic inbred maize line B104 during reproductive and vegetative stages (Wang et al., 2018b) (Table 1). Analysis of gene expression in the photosynthesis system between the WT and transgenic plants revealed that several genes were up-regulated in the transgenic plants when compared to the WT plants. Examples of genes up-regulated included GRMZM2G117572 (encoding the photosystem II PsbZ protein), GRMZM2G414660 (encoding the photosystem II cytochrome b599 subunit) and GRMZM5G831399 (encoding the photosystem II PsbH protein) among others.

Analysis of the co-expression between miR169, miRNA family, and ZmNF-YA TFs in transgenic Nicotiana bethamiana revealed that mutations in deletion sites terminate the regulation of zma-miR169 (Luan et al., 2014). The expression levels of zma-miR169l, zma-miR169i, and zma-miR169a were all inversely correlated with ZmNF-YA11, ZmNF-YA6, and ZmNF-YA7 over the short term. However, over the long term, the expression levels of all the NF-YA genes and miR169s decreased, revealing that ZmNF-YA11, ZmNF-YA6, and ZmNF-YA7 could not have been regulated by zma-miR169 in response to PEG stress after 15 days. Majority of the zma-miR169s were up-regulated by external ABA and down-regulated by drought stress but showed an early increase in expression and later a decline in response to salinity stress. Recently, Su et al. (2018) identified a NF-Y TF designated as ZmNF-YA3. Genome-wide analysis revealed that ZmNF-YA3 was linked to more than 6,000 sites in the maize genome, 2,259 of which are linked with genic sequences. Moreover, it was shown that ZmNF-YA3 could significantly improve high temperature and drought tolerance in maize by binding to the promoter region of three downstream genes (ZmMYC4, ZmbHLH92, and ZmFAMA).

In conclusion, all of the insights obtained above suggest NF-Y TFs play an important role in abiotic stress tolerance in maize by regulating several vital downstream genes involved in important aspects of abiotic stress responses, and plant growth and development, for instance, photosynthesis and ER stress response. Therefore, NF-Y TF genes could be engineered in maize and other crops in order to improve their abiotic stress tolerance, leading to improved production.

Engineering of TFs

The recent discovery of TFs as potential tools in the manipulation and engineering of quantitative traits such as drought and salinity has ignited the development of novel technologies based on TFs and benefiting not only gene discovery but also crop improvement. Engineering of TF activity has been a major target in these efforts, a direction that offers future promises in modulating metabolic pathways. For example, overexpression of DREB2 resulted in no stress tolerance improvement because proteins are composed of domains that limit the induction of their target genes downstream (Liu et al., 1998). Sakuma et al. (2006) obtained drought-tolerant plants by removing this repressor function through the engineering of point mutations. An undesirable effect of overexpressing stress-related TFs is that sometimes it negatively affects the growth and development of a plant leading to stunted growth or toxicity (Hussain, Amjad & Amjad, 2011). Elsewhere, overexpression of ZmDREB2A under a stress-activated promoter in the transgenic plants led to significant improvement in drought tolerance (Qin et al., 2007).

Transcriptional down regulators that repress gene expression in response to various abiotic stresses are also important tools in manipulating drought tolerance. For example, overexpression of a yeast transcription repressor CaZPF1 in Arabidopsis led to drought tolerance in transgenic plants (Kim et al., 2004). In the model plant Arabidopsis, systematic analysis of TF families resulted in the discovery of target genes that have the potential to enhance abiotic stress tolerance in major crops (Riechmann et al., 2000). A good example is the discovery of AtNF-YB1 gene that belongs to the Nuclear factor Y TF family (Nelson et al., 2007). The orthologue of (AtNF-YB1) gene in maize (ZmNF-YB2), when overexpressed in transgenic maize, resulted in drought-tolerant crops (Table 2). These findings emphasized the significance of TFs, especially when used in the engineering of plants.

The abiotic stress response networks in plants are very complex due to the large number of gene families involved and the complicated associations between the cis-acting elements and the TFs. In addition, a single TF may regulate a large number of target genes with similar cis-elements whereas TFs from different families may regulate a single target gene with different types of cis-acting elements (Hussain, Amjad & Amjad, 2011). Therefore, abiotic stresses regulating TFs not only function independently but also co-regulate abiotic stress responses between each other (Wang, Shao & Tang, 2016b) (Fig. 2). As mentioned throughout this review, genetic engineering of TF genes will be much more significant than manipulating a single functional gene. Thereafter, validation of the identified genes should be performed in model crops as well as the main crops by utilizing a stress-inducible promoter to reduce the detrimental effects brought about because of overexpression of certain TFs (Hoang et al., 2017). Moving forward, all of these advances will help elucidate the detailed regulatory channels taking part in multiple abiotic stress responses in plants, leading to the acquisition of target TF genes for enhanced breeding of abiotic stress-tolerant plants with improved desirable qualities and yields.

Current and post genomics approaches

Abiotic stresses represent a combination of various distinct traits consisting of a quantitative pattern of inheritance. Therefore, in order to efficiently understand the plants response to the different abiotic stresses at the molecular level, a deeper understanding of the systems involved in transcription regulation is required. Trait mapping, functional characterization, genomic selection, rapid RNA, and DNA high-throughput SNP genotyping tools, sequencing technologies, and other platforms are currently used to analyze the genetic mechanisms of different abiotic stresses including drought, salinity, and cold in an effort to speed up the breeding process in maize (Nepolean et al., 2018).

Genome editing techniques are the most recent technologies applied in gene function analyses and manipulations. RNA interference is a rapid and inexpensive technique utilized to analyze gene function in targeted gene knockdown analyses (Rabara, Tripathi & Rushton, 2014). However, a disadvantage of this technique is that the inhibition of gene function is not complete and this could lead to unintended off-target effects leading to misinterpretation of results (Gaj, Gersbach & Barbas, 2013). Of the targeted genome editing approaches currently available, clustered regulatory interspaced short palindromic repeats “CRISPR” is the most effective system used in editing plant genomes (Cong et al., 2013). CRISPR artificial transcription factors (CRISPR-ATFs) are gaining popularity as an effective system for regulating in vivo plant gene expression (Lowder et al., 2018). For instance, two novel systems (CRISPR-Act2.0 and mTALE-Act) were developed that could be used to study GRNs and the control mechanisms involved in plants (Lowder et al., 2018).

The other systems are transcription activator-like effectors nucleases (Boch et al., 2009) and Zinc-finger nuclease (Kim, Cha & Chandrasegaran, 1996). Another approach with huge potentials in functional genomics in plants is targeting-induced local lesions in genomes (TILLING). For example, a TILLING approach known as ecotilling, which was used to identify variations in natural populations, was successfully used to identify TFs in rice associated with drought tolerance (Yu et al., 2012). These techniques are vital in the selection of better quality genotypes and target genes in the abiotic stress tolerance research in maize.

Another approach currently being explored is the use of machine learning in the study of TFs GRN. Predictions of TFBSs and their corresponding transcription factor target genes (TFTGs) using machine learning approaches has made substantial contributions to the study of GRNs (Cui et al., 2014). Understanding the interplay between TFs, TFBSs, and TFTGs is vital in understanding the mechanisms involved in the gene regulatory processes taking place during biotic and abiotic stress responses in plant (Shinozaki & Yamaguchi-Shinozaki, 2006). Various computational algorithms are available in form of software packages. Additionally, expansive use of these software packages has revealed that even though some techniques were developed for one species, the same techniques can be used to analyze the dataset from other species (Cui et al., 2014). For example, a combination of Context Likelihood of Relatedness algorithm analyzed on Escherichia coli (Faith et al., 2007), Double two-way t-tests algorithms analyzed on Escherichia coli and Learning Module Networks algorithm tested on yeast (Joshi et al., 2009) was used to identify the presence of oxidative stress regulatory TFs in Arabidopsis (Vermeirssen et al., 2014). Moreover, The algorithm for the reconstruction of GRNs (Margolin et al., 2006) was established to deduce transcriptional regulations in human immune B cells, but was later used to deduce transcriptional interactions regulating root physiological and developmental processes in Arabidopsis (Chávez Montes et al., 2014).

Gene regulatory networks provide insights into the relationships between TFs and their corresponding target genes (Koryachko et al., 2015). For instance, network component analysis (NCA), a computational method developed for analysis of TF-gene interactions in microbial TF-GRNs, was employed to quantitatively analyze TF-GRNs critical in floral development in Arabidopsis (Misra & Sriram, 2013; Ni et al., 2016). The results showed that the NCA model adequately accounted for the total gene expression analysis in a TF-GRN of seven TFs (AG, HY5, SEPALLATA3, AP3/P1, AG, AP2, and AGL15) and 55 genes. Strong interactions were present between different TF-gene pairs, such as, LFY and MYB17, AG and CRC, AP2 and RD20, AGL15 and RAV2, and finally HY5 and HLH1. In maize, a machine learning algorithm GENIE3 was used together with numerous RNA-Seq expression data to establish a four tissue (root, SAM, seed, and leaf) specific GRNs (Huang et al., 2018). The results showed that even though many TFs were expressed in multiple tissues, a multi-level examination predicted regulatory roles for many TFs. Additionally, 76.6% (30,028/39,479) of the genes were found to be expressed in all the maize tissues. Out of the total of 2,587 TFs annotated by GRASSIUS in maize (Chen et al., 2013), 54.46% were expressed in all the four tissues while 86.63% of the total TFs were expressed in at least one of the four tissues.

Understanding the mechanisms of GRNs is vital in gaining insights on how TFs control gene expression in response to various abiotic stresses. Wet lab experiments are technically demanding, time-consuming and financially demanding (Penfold & Wild, 2011). Many machine-learning approaches have been proposed with an aim of reducing costs and time spent in the prediction of GRNs. For instance, recent development of a publicly accessible maize TF ORF collection (TFome) consisting of 2,034 clones that correspond to 2,017 unique maize TFs and co-regulators (CoREGs), has vastly contributed to the better understanding of GRNs (Burdo et al., 2014). The TFome was generated from a set of full cDNAs obtained from the Arizona Genomics Institute. The synthesis information, generated sequences, and request links for the maize TFome information are publicly available through GRASSIUS ( In conclusion, adaptation of available crop databases such as Gramene (Tello-Ruiz et al., 2018), and GRASSIUS for maize in machine learning approaches, as well as developing and adopting new databases, for example, the Wheat Information System (Hu, Scheben & Edwards, 2018) will help in the storage of data at the same time making it more accessible to scientists.

Traditional breeding techniques for selecting desirable traits depend on the observed phenotypic traits which can be misleading sometimes during selection, and this has led to low success in such strategies. Genomic selection is an accurate and efficient approach when it comes to the prediction of genotypic performance in crops. In maize, utilization of genomic techniques in the manipulation and analyses of TFs has been reported in a few studies. For instance, Shikha et al. (2017) utilized genomic selection techniques on 240 subtropical maize lines during exposure to drought by selecting 29,619 SNPs. The study found that 77 out of 1,053 SNPs were linked with 10 drought associated TFs located inside a 150 kb area. For example, MYB (149 kb), WRKY (125 kb), NAC (149 kb), bZIP (92 kb), and AP-ERF (148 kb) among others. Similarly, transcriptome analysis of two maize inbred lines using RNA-Seq showed that a total of 2,558 and 555 genes responded to drought in both the sensitive and the tolerant lines, respectively (Zhang et al., 2017a). TFs were found to be enriched in the genotype-specific responsive genes, and the genotypic differentially expressed genes (DEGs). It was postulated that the differential expression of 22 TF genes and the genotype-specific response of 20 TFs in the tolerant line might play an important role in drought tolerance enhancement in maize. Zhang et al. (2017b) utilized RNA-Seq platform to analyze the expression of TFs in response to lead stress in a maize 178 lead-tolerant line. In this study, a total of 464 genes were expressed, among which 262 differentially expressed TFs which responded to Pb treatment were identified. More recently, (Zhao et al., 2018) mapped several abiotic stress responsive TFs to QTLs. The results showed that MYB78 and hsp70 were mapped to mQTL1-5. On chromosome 6, pep7 and mlip15 were both mapped on mQTL6-1. Kusano et al. (1995) demonstrated that mlip15 was a low-temperature activated gene that encodes a bZIP protein made up of 135 amino acid. Elsewhere, global transcriptome profiling using RNA-seq on B73 maize seedlings exposed to heat, drought, cold stress, and salinity revealed 5,330 DEGs (Li et al., 2017). Functional annotations of these DEGs suggested that the pathways involving TFs, hormone metabolism and signaling among others controlled the stress responses. Among the 5,330 DEGs obtained, 167 genes were common to the four abiotic stresses; these included two down-regulated TFs (one MYB related and one b-ZIP) and 10 up-regulated TFs (one ARF, five ERFs, one MYB, one HD-ZIP, and two NAC). This study significantly contributes to a deeper understanding of molecular mechanisms involved in maize leaf responses to different abiotic stresses and could eventually contribute to the development of maize cultivars that are tolerant to various abiotic stresses.

Approaches involving genome-editing techniques create possibilities allowing for gene knockouts, point mutations, epigenetic changes, and the activation or repression of genes (Kamburova et al., 2017). Svitashev et al. (2016) reported the use of biolistic delivery of Cas9-gRNA ribonucleoproteins in maize cells, and this approach resulted in plants with both edited and mutated alleles. Recently (Cox et al., 2017), reported the use of single-effector programmable RNA guided RNases Cas13. This marks a major leap in plant transformation opening new opportunities in accelerated breeding in other main crops such as wheat, soybeans, sorghum, and rice. By using the RNA editing tools, the DNA structure is left intact but the function of the TF genes is manipulated. Utilization of genome editing techniques is still in its infancy and it is yet to be fully explored for abiotic stress tolerance in maize.

Future outlook

Recent advances in genomics, molecular biology, metabolomics and proteomics have yielded fresh insights into the plant GRN, composed mainly of regulatory elements (trans-elements and cis-elements), inducible genes (developmental and environmental cues), varying signal factors, and complementary biochemical pathways (Tang, Harris & Newton, 2003; Wang et al., 2003; Zhu, 2002). Sequencing of the whole maize genome has provided a basis for the functional characterization and identification of genetic networks and genes for maize improvement (Schnable et al., 2009). Moreover, recent availability of transcriptome profiling technologies, including genome sequencing and DNA microarrays, has opened new doors for understanding the patterns of transcription in the area of plant growth and development (Sekhon et al., 2011).

Understanding the genetic architecture of the molecular networks involved in maize, by utilizing current “OMICS” technologies is urgently needed to unravel the drought, heat and salt tolerance mechanisms in maize. Numerous genetic studies have shown that abiotic stress tolerance traits are usually polygenic making the selection of such traits extremely difficult (Ciarmiello et al., 2011). With the recent whole-genome sequencing of the B73 maize line, it’s now feasible to identify most maize TFs and systematically estimate their contribution to abiotic stress tolerance. Maize has an increased level of genetic disequilibrium linkage (LD) and genetic diversity making it an ideal plant species since the LD and genetic diversity have been predicted to be within a number of kilobases (kbs) in maize landraces (Tenaillon et al., 2001). This characteristic makes genome-wide association studies (GWAS) at the gene level more accurate when compared to self-pollinated plant species as long as genome-wide and high-density DNA markers are present (Yan, Warburton & Crouch, 2011; Li et al., 2012). For example, using a Bayesian-based genome-wide association method in which RNA-seq-based systems of transcript buildup were utilized as explanatory variables (eRD-GWAS), genes linked to 13 traits were discovered from a group of 369 inbred maize lines (Lin et al., 2017). Additionally, TFs were found to be considerably enriched among the trait-associated genes discovered with eRD-GWAS. Similarly, genome-wide analyses carried out on the maize B73 inbred line to identify all the Hsf genes identified 25 non-redundant Hsf genes designated as ZmHsfs (Lin et al., 2011). In soybean, an all-inclusive phylogenetic study revealed 58 dehydration responsive genes from the GmNAC TF family (Le et al., 2011). RNA sequencing performed on 14-day old maize seedlings of inbred lines Mo17, B73, PH207, B37, and Oh43 under heat, cold, and control treatments, revealed a large number of genes that responded differentially between parental inbred lines (Waters et al., 2017). Moreover, 20 of the 57 annotated TF families in maize were enriched for elevated genes in heat and/or cold stress in at least three of the five inbred genotypes. Finally, TF families with TFs that were enriched for up-regulated genes in response to heat stress included MYB and HSF TF families, while 18 TF families with TFs enriched for up-regulated genes in response to cold stress included APETALA2/(AP2/EREB).

A new approach currently gaining rapid popularity is the field of phenomics. By utilizing high-throughput phenotyping, various physiological parameters such as biomass, internode length, leaf area, chlorophyll content, plant width and height, and growth rate can be accurately determined in real time, and noninvasively (Rabara, Tripathi & Rushton, 2014). Large amounts of quality phenomics data can be generated for many transgenic plants. Currently, field phenotyping systems are being developed with the capacity to determine whether the engineering of TFs in plants can improve abiotic stress tolerance (Rabara, Tripathi & Rushton, 2014). For instance, Awlia et al. (2016) demonstrated that the phenotyping of polygenic traits in one experimental study could provide new insights into the mechanisms of plant responses to different abiotic stresses. The establishment of new phenomics technologies will further strengthen the use of forward genetics in the identification of novel TF genes regulating plant responses to different abiotic stresses.

Since TFs tend to regulate multiple pathways as opposed to a majority of the structural genes, they offer a powerful and unique system for use in the control of complex regulatory networks in plants. Overexpression of genes regulating the transcription of several down-stream abiotic/drought stress regulatory genes is a much better approach in the engineering of drought tolerant/resistant plants as opposed to the development of specific functional genes (Bartels & Hussain, 2008). Development of transgenic plants with enhanced abiotic stress tolerance by regulating TFs has become an important aspect of abiotic stress tolerance. Members of the WRKY, MYB, AREB, and bZIP, TF families have recently been utilized in the regulation of abiotic stress responses in major crops (Singh, Foley & Oñate-Sánchez, 2002). Many of the members belonging to these TF families have been identified and characterized in Arabidopsis, whose genome has been analyzed using microarray analysis, thus leading to the discovery of potential genes (Shinozaki, Yamaguchi-Shinozaki & Seki, 2003; Bray, 2004; Denby & Gehring, 2005). Thus, TF families offer important targets for use in gene manipulation and regulation which could be vital in understanding responses involved in abiotic stress tolerance. An increasing trend has seen the engineering of TFs involved in stress-signaling networks using biotechnology tools to generate transgenic stress tolerant plants. (Abe et al., 2003; Sakuma et al., 2006).


The population in our planet is projected to rise to nine billion by the year 2050 (Hussain, 2006), together with the rapid changes in climate there is an urgent need to speed up the productivity of major crops. Understanding molecular mechanisms and mining stress-responsive genes that control plant responses to different abiotic stresses is a major prerequisite in the development of stress-resistant and high yielding crop varieties (Khan et al., 2018). To safeguard the global food production, crops (like maize) that are well adapted to adverse environmental conditions should be established (Vinocur & Altman, 2005; M’mboyi et al., 2010).

Maize is highly affected by abiotic stresses especially drought throughout its growth cycle, with the most damage being seen during the developmental stage and prior to flowering (Claassen & Shaw, 1970). TF mediated research in plants has recently shown progressive improvement since most of the TF encoding genes are early stress-responsive genes which control the expression of various downstream target genes (Hoang et al., 2017). This has in turn led to a deeper understanding of the involvement and functions of TFs in plant responses to different abiotic stresses (Bartels & Sunkar, 2005).

This review emphasizes on the main TF families and their potential in abiotic stress tolerance in maize. The majority of the TF genes in the literature are reported to play major roles in multiple abiotic stress tolerances. Among the target genes for engineering, the utilization of TFs has been recommended as they have potential to revolutionize biotechnology upon which novel crops with improved tolerance to abiotic stresses could be successfully generated. There is absence of literature available on abiotic stress responsive TFs with agronomic traits that have been utilized in maize in field conditions. Although Monsanto has developed, a biotechnology-derived inbred maize line that expresses HB17 (ATHB17), a TF from Arabidopsis (Park et al., 2013; Hymus et al., 2013). Expression of ATHB17 in the inbred line is linked with increased ear biomass at the silking stage compared to the near-isogenic controls (Rice et al., 2014). Increased ear biomass at the early stage of plant development is associated with increased silk size and greater grain yield from hybrid maize (Borrás & Westgate, 2006; Lee & Tollenaar, 2007).

Transcription factors are excellent candidates for the development of transgenic crops because of their roles in plant growth and development. Incorporation of abiotic stress response pathways in the vital reproductive and vegetative development stages in crops is an efficient strategy to improve productivity in field conditions (Nelson et al., 2007). TFs can be used to simulate a variety of developmental and biochemical networks that take part in the regulation of abiotic stresses, thus increasing the performance of crops in response to multiple plant abiotic stresses. Joshi et al. (2016) noted that overexpression of several TF genes significantly enhanced abiotic stress tolerance but at the same time caused a number of negative effects including lower yields, late flowering, and dwarfing in transgenic plants. This should be considered in future studies to maximize the effectiveness of TF engineering in responses to different abiotic stresses.

Moving forward, identification and characterization of multiple stress regulatory genes should be given more focus not only in maize but also in other major crops to target the most effective genes that can be universally used to develop abiotic stress tolerant crop varieties. Machine learning algorithms can be integrated with transcriptome data and high-throughput phenotyping data to further increase the automation of the gene discovery processes such as genome annotation and GRNs predictions.

Genetic engineering of multiple stress regulatory TF genes is a strong candidate for the enhancement of stress tolerance in plants when compared to focusing on a single individual gene. Nevertheless, recent advances in maize breeding, genomics, and functional analysis of genes combined with high-throughput sequencing technologies have significantly increased the chances of achieving multiple stress tolerances. The identification of commercial transgenic plants with enhanced crop performance under stress conditions is a tedious, expensive, and lengthy process. However, the successful genetic engineering of maize for improved abiotic stress tolerance using TFs as reviewed herein confirms this approach is feasible.

Since maize is a major crop in many countries, there is need for more collaboration in both applied and theoretical genomics in order to improve the production of maize. The rapid advancements in TFs genome analysis currently being witnessed are mostly on temperate maize varieties. It is hoped that these technologies can be transferred to subtropical and tropical maize varieties that serve as essential food security crops in developing countries.

64 Citations   Views   Downloads