Genetic variation and forensic efficiency of 30 indels for three ethnic groups in Guangxi: relationships with other populations

Aim In this study, we used a series of diallelic genetic marker insertion/deletion polymorphism (indel) to investigate three populations of Yao, Kelao, and Zhuang groups in the Guangxi region of China and to evaluate their efficiency in forensic application. Result No deviations for all 30 loci were observed from the Hardy–Weinberg equilibrium after Bonferroni correction (p > 0.05/30 = 0.0017). The allele frequencies of the short allele (DIP-) for the above three populations were in the range of 0.0520–0.9480, 0.0950–0.8780, and 0.0850–0.915, respectively. The observed heterozygosity of the 30 loci for the three populations was in the ranges 0.0802–0.5802, 0.1908–0.6053, and 0.1400–0.5600, respectively. The cumulative power of exclusion and combined discrimination power for Yao, Kelao, and Zhuang groups were (0.9843 and 0.9999999999433), (0.9972 and 0.9999999999184), and (0.9845 and 0.9999999999608), respectively. The DA distance, principal component analysis, and cluster analysis indicated a clear regional distribution. In addition, Zhuang groups had close genetic relationships with the Yao and Kelao populations in the Guangxi region. Conclusion This study indicated that the 30 loci were qualified for personal identification; moreover, they could be used as complementary genetic markers for paternity testing in forensic cases for the studied populations.


INTRODUCTION
Autosomal short tandem repeat (STR) is a standard marker for DNA analysis in forensic practice. However, STR mutations have always troubled the paternity testing. Compared to the mutation rates of STR (about 10 -3 ), Insertion/deletion polymorphism (indel) markers have significantly lower mutation rates (less than 10 -8 ) (Sobrino & Carracedo, 2005). However, single nucleotide polymorphisms (SNPs) have a low mutation rate, it is based on the sequence polymorphism rather than length polymorphism that is difficult to achieve simple and rapid genotyping in the routine forensic lab (Weber et al., 2002). Insertion/deletion polymorphisms are prospective genetic markers and spread widely throughout the genome (Nachman & Crowell, 2000); moreover, they also combine the desirable characteristics of both STRs and SNPs. Insertion/deletion polymorphism is a length polymorphism marker and it can be easily analyzed with capillary electrophoresis (Pereira et al., 2009). In totality, indels are considered to be promising markers in forensic application.
The Investigator DIPplex kit was the first commercial kit developed by Qiagen (Qiagen, Hilden, Germany) for the indel marker. This kit contains 30 autosomal indels and amelogenin, and it has been used to perform systematic investigations on worldwide populations of African (Hefke, Davison & D'Amato, 2015), Asian (Wang et al., 2014;Liang et al., 2013;Meng et al., 2015;Seong et al., 2014;Wei et al., 2014;Yang et al., 2017), European (Friis et al., 2012;Kis et al., 2012;Martin et al., 2013), and American (Saiz et al., 2014) origins. However, very few studies have reported about how indels can be used in comprehending the genetic variation of ethnic minority groups (Zhuang, Yao, and Kelao) in the Guangxi Zhuang Autonomous Region, China. Therefore, we used the kit to understand population polymorphism of Yao, Kelao, and Zhuang ethnic groups in the Guangxi region and to evaluate the efficacy of this kit. Moreover, the genetic differentiation in the various populations was analyzed by comparing the results of the studied populations with those of other reported populations.
Guangxi Zhuang Autonomous Region is located in southwest China and adjacent to Guangdong, Guizhou, Yunnan, and Hunan provinces. One of the settlements of Chinese ethnic minorities is located in this region; moreover, the immigration and symbiosis of multiple ethnic groups have witnessed a fine balance in this region. Among the 11 ethnic minorities in the Guangxi region, the Zhuang group is the native inhabitant of Guangxi region; the tribe members are descendants of the Xi'ou and Luo'Yue clans that have been distributed in Guangxi since ancient times (Sun et al., 2013). The Zhuang is the largest ethnic minority group in China, about 87.77% of the Zhuang population is concentrated in the Guangxi region. Furthermore, the Kelao group migrated to the Guangxi region from Guizhou province, and the exodus of this tribe happened hundreds of years ago as this population group was fleeing from the famine-affected region of Guizhou in those times (Sun et al., 2013). During the reign of the erstwhile Sui and Tang dynasties, the Yao group moved to Guangxi from the present-day provinces of Hunan and Guangdong in China (Sun et al., 2013). According to the data released in 2010 census, the populations of the ethnic groups, Zhuang, Yao, and Kelao, are about 14.82 million, 1.349 million, and 2,900 people in the Guangxi region, respectively; the Yao is second only to the Zhuang group in terms of population sizes, while the population of the Kelao group is the lowest among the 11 ethnic groups of Guangxi region. (http://www.stats.gov.cn/ english/statisticaldata/censusdata/rkpc2010/indexch.htm). Moreover, the Zhuang language, Yao language, and Kelao language all belong to the Sino-Tibetan language.
In this study, the genetic data of these myriad types of populations based on 30 indels was investigated, and the results were further analyzed to evaluate whether they could be used in forensic applications and population genetic studies.

Sample collections and DNA extraction
Bloodstain samples were collected from unrelated volunteers living in the Guangxi Zhuang Autonomous Region of China. The population sample sizes were as follows: Yao (N ¼ 162), Kelao (N ¼ 152), and Zhuang (N ¼ 200). As described earlier by Walsh, Metzger & Higushi (2013), the Chelex-100 method was used for the extraction of genomic DNA from bloodstain samples. Informed consent was obtained from all the individuals and this study was approved by School of Forensic Medicine, Southern Medical University.

Genotyping and amplification
In this study, PCR amplification was performed using the Investigator DIPplex kit handbook in accordance with the manufacturer's instructions (http://www.qiagen.com/ products/investigatordipplexkit.aspx) in a GeneAmp PCR system 9700 thermal cycler (Applied Biosystems, Foster City, CA, USA). The PCR products were detected with ABI 3130XL Genetic Analyzer (Applied Biosystems, Foster City, CA, USA). Genotypes were determined by GeneMapper ID-X software v1.3 (Applied Biosystems, Foster City, CA, USA). In addition, 9948 DNA (Promega, Fitchburg, WI, USA) was employed as a positive control in amplification.

Quality control
We performed the study in accordance with the ISFG recommendations for DNA polymorphism analysis, and the procedure was described by Schneider (2007).

Forensic parameters
The allele frequencies and forensic parameters of 30 indel loci in the three ethnic populations are presented in Table S1. The allele frequencies of the short allele for Yao, Kelao, and Zhuang ethnicities were in the range of 0.0520-0.9480, 0.0950-0.8780, and 0.0850-0.9150, respectively. The PE for the 30 indels was less than 0.3 with respect to Yao, Kelao, and Zhuang groups; thus, the PE value was much lower than those of most STRs (Deng et al., 2007;Guo, 2017;Jin et al., 2004). This implies that more loci are needed in indels to achieve the same value of the cumulative power of exclusion (CPE) than that for STR. The highest DP was observed at the following positions for the three groups: HLD48 (DP ¼ 0.6520) for Yao, HLD48 (DP ¼ 0.6111) for Kelao, and HLD56 (DP ¼ 0.6494) for Zhuang. The polymorphism information content (PIC) was in the range of 0.0945-0.3750, and 67% of PIC values (20 out of 30) was over 0.3 in Yao samples. Then, the PIC values were in the range of 0.1577-0.3750, and more than 77% (23 out of 30) was over 0.3 in Kelao samples. Finally, the PIC values were in the range of 0.1435-0.3750, and more than 70% (21 out of 30) was over 0.3 in Zhuang samples. The above data indicate that polymorphism of indels is lower than STR; this occurs because an indel is a diallele with only two alleles per locus. The Ho for Yao, Kelao, and Zhuang samples are in the ranges 0.0802-0.5802, 0.1908-0.6053, and 0.1400-0.5600, respectively. The Ho of the seven loci in Yao samples, six loci in Kelao samples, and eight loci in Zhuang samples were less than 0.3 per experimental observations. The results indicate that some indel markers are relatively polymorphic while some indels exhibit rather low levels of polymorphism in the studied populations, such as HLD39, HLD64, HLD99, HLD111, and HLD118.
In the three populations, the departures from the HWE were observed at the HLD125 locus in Yao population, whereas the same parameter was observed at HLD45, HLD83, HLD114, HLD124, and HLD136 loci in Kelao population. After applying the Bonferroni correction (p > 0.05/30 ¼ 0.0017), we could not observe any deviation from HWE. As displayed in Table S2, the CPE and CDP for the Yao, Kelao, and Zhuang samples were (0.9843 and 0.9999999999433), (0.9972 and 0.9999999999184), and (0.9845 and 0.9999999999608), respectively. A high level of DP was observed in the three sample populations (CDP > 0.9999), indicating the sufficient potential of 30 indels in forensic individual identification. However, the CPE was less than 0.9999, which indicates that 30 indels were not effective enough for paternity testing. Therefore, the DIPplex kit can serve as a supplement to the current STR system for paternity testing.

Linkage disequilibrium analysis
An analysis of linkage disequilibrium that occurs between 30 indels was performed by SNPAnalyzer software. As is shown in Fig. 1, the pattern of linkage disequilibrium was revealed in a reverse triangle, and the intensity of red color in the plot is a measure of whether the linkage disequilibrium is strong in magnitude. The level of LD between 30 indel loci was estimated using r 2 tested by the SNPs Analyzer program. With only HLD88 and HLD92 (r 2 ¼ 1) as exceptions, the r 2 values of all loci were less than 0.8 in Yao samples. This means that HLD88 were linked with HLD92 in the Guangxi Yao samples. This probably occurs because the sample size of Yao individuals is too small.

Population comparisons
The genetic distances (D A distance) were calculated among Yao, Kelao, and Zhuang samples, and the 20 referenced groups included Beijing Han (Wei et al., 2014)

Principal component analysis
To perform PCA, we used MATLAB 2007a software (Tan et al., 2014); the analysis was completely based on the allele frequencies of Yao, Kelao, Zhuang, and 20 referenced groups. The proportions of first and second components were 59.66% and 16.69%, respectively. In addition, the two components occupied 76.35% of the total variance. As shown in Fig. 3, the result indicated a clear regional distribution. In addition, Yao, Kelao, Zhuang, and the other 11 East Asian groups were located on the left midline of the distribution, whereas Kazak and Uighur were located on the right middle section. Four European groups were located on the upper right quadrant near the midline and close to the Uruguayan group, whereas Jalisco Mexican group was located on the right upper quadrant. In addition, Nigeria was located on the lower right quadrant.

Population STRUCTURE analysis
Population structure analysis was performed using the STRUCTURE program with 10,000 burn-in period and additional 10,000 Markov Chain Monte Carlo replication; and the K values were set to 2-7 and each K was run in 15 replicates (Falush, Stephens & Pritchard, 2003). As shown in Fig. 4, the 28 groups were clarified clearly into distinct geographic patterns. When K at 2 and 3, East Asian groups, North American groups and European groups could be differentiated by distinct discrepancy of color compositions. Statistically, K ¼ 4 is the best K value. When K at 4, the constituents of three populations of Guangxi region and the other 11 East Asian groups exhibited a mixture of red and green, whereas the six components of North American group are almost entirely blue. Meanwhile, the four European groups and Uruguayan group exhibited a mixture of yellow, blue, and green components. Meanwhile, Eurasia populations (Kazak and Uigur groups) also exhibited a mixture of yellow, blue, and green components, where in the proportion of green component was higher. In addition, the main constituent is yellow in the African groups. At K > 4, we did not observe any further substructure. Hence, the

Alleic polymorphisms and forensic statistical parameter analysis
The allele frequencies of 30 indel loci could distinguish different populations to a certain degree, and the results revealed that Guangxi three ethnic groups were similar to the East Asians, especially with most Chinese populations in allele frequency distributions.
In the forensic application field, CPE and CPD values are common indicators to estimate the forensic efficiency. In this study, the CPE and CPD values for the Yao, Kelao, and Zhuang samples were 0.9843 and 0.9999999999433, 0.9972 and 0.9999999999184, and 0.9845 and 0.9999999999608, respectively. The high CPD value clarified that these 30 indel loci could be regarded as efficient genetic markers in forensic identification cases, while the relatively lower CPE value indicated that the 30 loci could only be used as complementary genetic markers for paternity testing.

Linkage disequilibrium analysis
The indel loci are suitable for forensic applications as independent loci if no relevance exists between two loci from the same chromosome or two random chromosomes (Slatkin, 2008). The LD analysis indicated no significant LD among the 30 loci in Zhuang and Kelao groups, while HLD88 were linked with HLD92 in Yao sample. This probably occurs because the sample size of Yao individuals is too small. Beyond that, there was no significant LD among the loci which indicated independence from the other 30 indels in the Guangxi Zhuang and Kelao groups. Nonetheless, it is worth noting that the sample size is limited, and further studies are needed to help us to confirm our findings.

Population differentiations
Genetic distance reflected by D A distance is considered an effective analysis method to reveal the genetic divergences between populations within a species (Nei, Tajima & Tateno, 1983). Detailed data were shown in Dataset S4, and the genetic distance between Yao and Zhuang, Yao and Kelao, and Zhuang and Kelao were 0.0042, 0.0042, and 0.0011, respectively; thus, the genetic distances between Yao, Kelao, and Zhuang groups were very close. The results show the Kelao groups had closer relationships with Zhuang groups, indicating that Kelao groups in the Guangxi region might have been subjected to intensive gene exchange with Zhuang groups in ancient times (He et al., 2019). As shown in Fig. 2, the three Guangxi groups have a close genetic distance with most Asian populations, the values of D A genetic distance were consistent with the geographic locations of these populations. Compared with East Asian groups, Eurasian groups, European groups, Mexican groups, and Nigeria groups were found had more differences with Guangxi three ethnic groups. The results of the STRUCTURE analysis were roughly in line with population differentiation. From this analysis, 28 populations were classified into geographic patterns.

Principal component analysis
According to Fig. 3 (Li et al., 2003). Moreover, the distribution of the other populations was in accordance with geographical patterns.

CONCLUSION
In conclusion, we obtained the allele frequencies and forensic parameters of 30 autosomal indels loci for Yao, Kelao, and Zhuang groups in Guangxi. The set of 30 indels showed high efficiency in individual identification of these samples. The results of D A distance, PCA, and cluster analysis all showed that Zhuang groups had very close genetic relationships with Yao and Kelao groups in the Guangxi region. Furthermore, studies were performed in order to compare the three ethnic groups in Guangxi with more reference groups. All these results were helpful in providing a better understanding of the genetic background of people in the Guangxi region.