Ethylene inhibits stem trichome formation in Arabidopsis
- Published
- Accepted
- Subject Areas
- Cell Biology, Developmental Biology, Plant Science
- Keywords
- trichome, ethylene, CTR1, Arabidopsis, cellular differentiation, pattern formation, glucose, stem trichome, trichome branching
- Copyright
- © 2018 Gibson
- Licence
- This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, reproduction and adaptation in any medium and for any purpose provided that it is properly attributed. For attribution, the original author(s), title, publication source (PeerJ Preprints) and either DOI or URL of the article must be cited.
- Cite this article
- 2018. Ethylene inhibits stem trichome formation in Arabidopsis. PeerJ Preprints 6:e27047v1 https://doi.org/10.7287/peerj.preprints.27047v1
Abstract
Trichomes, specialized cells that form on the above ground parts of plants, are useful model systems for studying cell differentiation. In this study, the plant hormone ethylene was found to strongly inhibit formation of trichomes on stems of Arabidopsis thaliana. Plants grown in the presence of high concentrations of the ethylene precursor 1-aminocyclopropane-1-carboxylic acid fail to form trichomes on their primary inflorescences. In addition, plants carrying mutations in CTR1 that confer a constitutive response to ethylene exhibit severe reductions in stem trichome numbers. In contrast, plants carrying mutations that confer ethylene insensitivity, and plants grown in the presence of an ethylene biosynthesis inhibitor, produce normal numbers of stem trichomes. Together, these results suggest that either excess ethylene or a constitutive ethylene response prevents the normal differentiation of cells that would otherwise form stem trichomes. Reduced ethylene levels and decreased ethylene response, in constrast, appear insufficient to cause cells that do not normally form trichomes to form trichomes. In contrast to ethylene, application of exogenous Glc results in increased stem trichome numbers. Besides affecting stem trichome numbers, ethylene may also affect branching of stem trichomes. In Arabidopsis thaliana, the vast majority of stem trichomes are unbranched. When wild-type Arabidiopsis thaliana of the Col-0 ecotype are grown in the presence of an ethylene biosynthesis inhibitor, the percentage of stem trichomes that are branched increases significantly. However, growth in the presence of an ethylene biosynthesis inhibitor does not affect stem branching in wild-type Arabidopsis thaliana of the Ler-0 ecotype. Plants carrying the etr1-1 and ein2-1 mutations, which cause ethylene insensitivity, have an increased percentage of branched stem trichomes. In contrast, plants carrying the ctr1-1 and ctr1-12 mutations have a decreased percentage of branched stem trichomes. Growth in the presence of a precursor of ethylene biosynthesis also causes a substantial reduction in branching of Arabidopsis leaf trichomes, suggesting that ethylene has a negative effect on branching of both leaf and stem trichomes in Arabidopsis.
Author Comment
This is a submission to PeerJ for review.
Supplemental Information
Raw data for stem trichome numbers on ctr1 and wild-type lines
This file contains the raw data depicted in Figure 1.
Raw data for stem trichome numbers for wild-type plants grown in the presence and absence of ACC
This file contains the raw data depicted in Figure 2.
Raw data for effects of AVG on wild-type stem trichome numbers
This file contains the raw data depicted in Figure 4.
Raw data for stem trichome numbers for etr1-1 and ein2-1 plants
This file contains the raw data depicted in Figure 5.
Raw data for the effects of exogenous Glc on stem trichome numbers
This file contains the raw data depicted in Figure 6.
Raw data for effects of altering ethylene biosynthesis on stem trichome branching
This file contains the raw data depicted in Figure 7.
Raw data for effects of altering ethylene response on stem trichome branching
This file contains the raw data depicted in Figure 8.