Skip to main content

ORIGINAL RESEARCH article

Front. Plant Sci., 12 January 2018
Sec. Plant Breeding

Characterization of Linkage Disequilibrium and Population Structure in a Mungbean Diversity Panel

  • 1Centre for Tropical Crops and Biocommodities, Queensland University of Technology, Brisbane, QLD, Australia
  • 2Queensland Alliance for Agriculture and Food Innovation, University of Queensland, Warwick, QLD, Australia
  • 3Department of Agriculture and Fisheries, Hermitage Research Facility, Warwick, QLD, Australia

Mungbean [Vigna radiata (L.) R. Wilczek var. radiata] is an important grain legume globally, providing a high-quality plant protein source largely produced and consumed in South and East Asia. This study aimed to characterize a mungbean diversity panel consisting of 466 cultivated accessions and demonstrate its utility by conducting a pilot genome-wide association study of seed coat color. In addition 16 wild accessions were genotyped for comparison and in total over 22,000 polymorphic genome-wide SNPs were identified and used to analyze the genetic diversity, population structure, linkage disequilibrium (LD) of mungbean. Polymorphism was lower in the cultivated accessions in comparison to the wild accessions, with average polymorphism information content values 0.174, versus 0.305 in wild mungbean. LD decayed in ∼100 kb in cultivated lines, a distance higher than the linkage decay of ∼60 kb estimated in wild mungbean. Four distinct subgroups were identified within the cultivated lines, which broadly corresponded to geographic origin and seed characteristics. In a pilot genome-wide association mapping study of seed coat color, five genomic regions associated were identified, two of which were close to seed coat color genes in other species. This mungbean diversity panel constitutes a valuable resource for genetic dissection of important agronomical traits to accelerate mungbean breeding.

Introduction

Mungbean [Vigna radiata (L.) R. Wilczek var. radiata] is a grain legume originating from South Asia. It belongs to subgenus Ceratotropis of the Fabaceae family which comprises 23 species including the closely related wild mungbean [Vigna radiata var. sublobata (Roxb) Verdcourt]. As a summer legume species with a short growth duration (55–70 days from sowing to maturity) and the ability to fix atmospheric nitrogen, mungbean delivers economic, farming systems, and environmental benefits. The crop is vital to smallholder farmers in Asia with an annual production of 3.5–4.0 million tons where it represents an excellent cheap source of carbohydrates, high quality protein (dry seeds 27% protein), folate and iron (Day, 2013). Over the last three decades, the global consumption of mungbean has increased by 60% with a corresponding growth in production area up to 6 million hectares, concentrated mainly in South, East, and Southeast Asia (Kim et al., 2015). As an orphan crop of subsistence agriculture with limited genetic information available, mungbean improvement has relied on traditional plant breeding methodologies for most of its cultivated history (Fernandez et al., 1988; Humphry et al., 2002). In fact investment to-date in the development of new mungbean varieties has been low, resulting in a narrow genetic base of the crop leaving the crop vulnerable to many abiotic and biotic stresses. Additionally, progress in developing genomics tools to support molecular breeding activities for developing improved mungbean varieties has been very limited. However, the recent release of a reference genome for mungbean (Kang et al., 2014) provides new opportunities for mungbean genomic research (Kim et al., 2015).

Mungbean is a self-pollinated diploid species with a chromosome number of 2n = 22 with an estimated genome size of 543 mega bases (Mb) (Parida et al., 1990; Kang et al., 2014). The relatively small genome size makes it an attractive and valuable model for advancing the understanding of diversity and evolution of legume genomes. The domestication of mungbean is considered to have taken place approximately 3500 years ago (Kim et al., 2015) from a small number of elite founders. The domestication process has resulted in significant genetic bottlenecks in the cultivated mungbean genome (Lakhanpaul et al., 2000). Previous genetic diversity studies of cultivated and wild mungbean germplasm, using both morphological and molecular markers, have highlighted low levels of genetic diversity in cultivated mungbean compared to the broader diversity found in wild mungbean (Santalla et al., 1998; Saravanakumar et al., 2004; Sangiri et al., 2007).

Wild mungbean relatives are of critical importance to broaden the genetic diversity of cultivated mungbean given the important biotic and abiotic stress resistance genes they may contain, which have not yet been incorporated into cultivated material by breeding programs.

In fact the use of wild relatives to increase productivity has been successfully demonstrated in many other crops including sorghum (Jordan et al., 2011) and barley (Ellis et al., 2000). Previous studies of genetic variation in wild mungbean germplasm have reported valuable genes affecting important agronomical traits such as phenology (Rebetzke and Lawn, 2006a); growth, biomass, and seed yield (Rebetzke and Lawn, 2006b); root and shoot attributes (Rebetzke and Lawn, 2006c). These genes could be introgressed into cultivated mungbeans to increase the resilience of cultivated material and broaden the overall genetic base (Pandiyan et al., 2008). Introgression of traits from closely related wild relatives into cultivated mungbean has been reported to produce fertile progeny with favorable morphological characteristics (Lambrides et al., 1999). By contrast, Vigna mungo [V. mungo (L.) Hepper], or black gram, produces sterile progeny when hybridized to mungbean (Lambrides et al., 1999).

Dissecting the genetic basis of important agronomic traits, such as seed coat color, grain size, flowering time and disease resistance, are critical to manipulating and introgressing these traits precisely to achieve breeding goals. Traditionally, linkage mapping is the primary tool to identify genetic loci underlying traits of interest. A limited number of genetic linkage maps have been developed in mungbean (Lambrides et al., 2000; Humphry et al., 2002; Isemura et al., 2012), however, despite great efforts a comprehensive and saturated genetic linkage map of all 11 chromosomes has not been generated (Kim et al., 2015). Instead, high density maps developed from whole genome sequences (Kang et al., 2014) enable further advancement in alternative approaches to trait dissection, such as association mapping, also known as linkage disequilibrium (LD) mapping (Gupta et al., 2005; Abdurakhmonov and Abdukarimov, 2008). LD mapping takes advantage of historical recombination events in a diverse set of lines to identify the genetic basis of traits at a higher resolution than traditional genetic linkage mapping. The resolution of association mapping relies upon the extent of LD. The degree of LD has yet to be accurately determined in mungbean. In cultivated material of the closely related species soybean, high levels of LD have been reported (∼150 kb), potenitally caused by inbreeding, adaptation and human selection (Lam et al., 2010). By contrast LD in wild soybean species was considerably lower (∼75 kb), indicating wild germplasm could play a major role in influencing the dynamics of genome change.

This study aims to assess the genetic diversity, population structure, LD and mapping capabilities of a large and diverse mungbean germplasm panel using a high-throughput SNP genotyping platform. This study provides a unique genomic resource for genetic dissection of important agronomical traits to accelerate mungbean breeding.

Materials and Methods

Plant Materials

The mungbean diversity panel consists of 466 accessions representing the cultivated mungbean [Vigna radiata (L.) R. Wilczek var. radiata] germplasm held in Australia by the National Mungbean Improvement Program (Queensland, DAF). The material originated from various sources worldwide and represents the widest range of phenotypic traits observed and characterized by the mungbean breeding team over the past 50 years. These included seed coat color, seed size and weight, days to flower, days to maturity, plant habit, plant height, and reaction to key foliar diseases. Sixteen wild accessions [Vigna radiata var. sublobata (Roxb Verdcourt)] originating from Australia were also included in the study as a comparison to the diversty panel of cultivated mungbeans.

Genotyping

Total genomic DNA was extracted from bulked young leaves of a single plant per accession as described by DArT P/L (DArT1). The samples were genotyped following an integrated DArT and genotyping-by-sequencing (GBS) methodology involving complexity reduction of the genomic DNA to remove repetitive sequences using methylation sensitive restrictive enzymes prior to sequencing on next generation sequencing platforms (DArT2). The sequence data generated were then aligned to the mungbean reference genome sequence, Vradi_ver6 (Kang et al., 2014), to identify single nucleotide polymorphisms (SNPs) markers.

Phenotypic Data Collection

All 482 mungbean accessions were planted at Hermitage Research Facility, Warwick, QLD, Australia (28°12′ S, 152°5′ E), over the summer of 2015. The field trial design was unreplicated single field plots for each accession, 4.5 m2 in size containing an average of 130 plants. Seed coat color was qualitatively recorded based on five categories (green, black, brown, yellow, and speckled).

Analysis of Genetic Diversity

The polymorphism information content (PIC) of each DArTseq SNP marker was determined using the following formula: PIC = 1-Σ(Pi2)/n where Pi is the frequency of the i th allele and n is the total number of genotypes (Weir, 1990).

Estimation of Linkage Disequilibrium

The pairwise LD between SNPs genome-wide across the wild and cultivated mungbean genotypes was calculated based on the allele frequency correlations (r2) using the TASSEL program (v5.1.0) (Bradbury et al., 2007; Tao et al., 2013). Only r2 for SNPs with pairwise distance less than 500 kb of each chromosome were used to draw the average LD decay figure. The LD decay graph was drawn by fitting a smooth spline of averaged r2 over physical distance in R v3.3.1. The LD decay was calculated when the squared correlations of allele frequencies r2 decreased to half of its maximum value.

Analysis of Population Structure

Population structure of the 466 cultivated accessions was analyzed using a Structure-like Population Genetic Analyses in R package LEA (Falush et al., 2007). The number of subpopulations is determined using a cross-entropy criterion. The cross-entropy criterion is based on the prediction of a fraction of masked genotypes (matrix completion), and on the cross-validation approach. Smaller values of the cross-entropy criterion usually mean better runs. We perform runs for 9 values of K (K = 2:10), and choose the value of K for which the cross-entropy curve exhibits a plateau (K = 4).

Results of structure analysis were used to identify accessions representing the four sub-populations. An individual accession with more than 90% identity from a single sub-population was classified as representative of that sub-population. Genetic differentiation (Fixation index, FST) among the four sub-populations was calculated using R package PopGenome (Pfeifer et al., 2014).

Genetic relationships among cultivated accessions were also analyzed using principal coordinate analysis (PCA) performed in the software package DARwin v6.0 (Perrier and Jacquemoud-Collet, 2006).

Genome-Wide Association Mapping of Seed Coat Color

Association mapping was conducted using mixed linear model (MLM) controlling for Q and kinship (K) as fixed and random effects respectively in TASSEL 5.1.0. Minor allele frequency (MAF) > 0.01 was used to filter SNPs prior to analysis. Q was extracted from results of previous population structure analysis, which detected four sub-populations. K was calculated using Scaled IBS method implemented in TASSEL 5.1.0. Bonferroni correction was applied to set thresholds for P-value significant (0.05/n); n represented the number of SNPs used in trait-marker association analysis. The Manhattan plot was generated using the R package qqman (Turner, 2014).

Results

Germplasm Diversity Analysis

A total of 22,230 SNP markers were identified in the cultivated and wild mungbean populations, of those 16,462 were physically mapped across the 11 mungbean chromosomes (Supplementary Table S1). An average of 1,497 SNPs were identified per chromosome (from 903 SNPs on chromosome 3 to 2,306 on chromosome 7) with an average marker density of 57.81 SNPs/Mb (Table 1 and Figure 1). A total of 7,675 SNPs segregated within the cultivated population, with an average PIC value of 0.174. In contrast, 6,174 SNPs segregated within the wild population with an average PIC value of 0.305 (Supplementary Figure S1).

TABLE 1
www.frontiersin.org

TABLE 1. Genomic distribution of 22,230 single nucleotide polymorphisms (SNPs) physically mapped on 11 cultivated and wild mungbean chromosomes/unanchored scaffolds.

FIGURE 1
www.frontiersin.org

FIGURE 1. The distribution of polymorphism information content (PIC) genome-wide of 466 cultivated mungbean accessions. Heat maps on each chromosome represent SNP densities within a window of 500 kb.

Estimation of Linkage Disequilibrium

Linkage disequilibrium was estimated between all SNP markers over the 466 cultivated and 16 wild mungbean accessions. The squared correlations of allele frequencies r2 of the cultivated mungbean population decreased to half of its maximum value at approximately 100 kb physical distance compared to the wild mungbean population which had largely decayed by 60 kb (Figure 2). Additionally, individual chromosomes of the cultivated population were estimated, no substantial differences were observed (Supplementary Figure S2).

FIGURE 2
www.frontiersin.org

FIGURE 2. Linkage disequilibrium (LD) graph of cultivated and wild mungbean. LD is determined by squared correlations of allele frequencies (r2) against distance between polymorphic sites, color-coded as follows: cultivated accessions (green) and wild accessions (blue).

Population Structure of the Cultivated Population

Structure-like population genetic analysis was used to analyze the structure of the cultivated population (Figure 3). A range of sub-populations (K = 2:10) were tested and a K-value of 4 was determined to best capture the structure of the cultivated population based on minimal cross-entropy (Supplementary Figure S3). Representative accessions from the four sub-populations defined as being > 90% relationship to a single sub-population were further characterized using phenotypic data (Supplementary Table S2).

FIGURE 3
www.frontiersin.org

FIGURE 3. Population structure of 466 cultivated mungbean accessions at K = 4. Each vertical bar represents a single accession, the length of each bar represents the proportion contributed by each sub-population. Sub-population 1 (color-coded orange), sub-population 2 (color-coded pink), sub-population 3 (color-coded green), and sub-population 4 (color-coded red).

Sub-population 1 was made up of 25 accessions, there was limited passport data as the majority of lines are Australian commercial lines (Crystal, Jade-AU) or Australian breeding lines (e.g., M11122). Those accessions with passport data were mostly from Southern Asia, Taiwan, Thailand, Philippines, and Vietnam with uniformly green seed coats.

Sub-population 2 was comprised of 40 accessions and had the widest range of passport data, with the accessions predominantly from Middle Eastern countries including Afghanistan, Uzbekistan, Tajikistan, Kyrgyzstan and Iran, with single accessions from China, India, Netherlands, and Turkey. This sub-population also had the widest range of seed coat colors, although largely green with a number of speckled, a single yellow accession and additionally this was the only sub-population to contain brown seed coats.

Sub-population 3 contained the largest number of accessions (59) mainly derived from Southern Asian countries, Cambodia, Philippines and Thailand with single accessions from China, Hong Kong, India, Indonesia, and Vietnam. This sub-population also contained the highest number of accessions from Iran (6). Of the 59 accessions, 19 displayed yellow seed coats while the remaining accessions were green in color with two speckled seed coats.

Sub-population 4 contained the lowest number of accessions (22), and the majority of the accessions did not have passport data; those that did were from India and Pakistan with a single line from Taiwan. Seed coat colors were primarily green with three accessions displaying speckled seed coats.

Principal coordinate analysis was also used to visualize the relationships amongst the cultivated accessions in the panel. When the four sub-populations were plotted they clustered toward the extremities of the plot based on their genetic differences (Figure 4). The first two principal coordinates accounted for approximately 34.04% of the genotypic variance with coordinates one (x-axis) and two (y-axis) explaining 18.18 and 15.86%, respectively.

FIGURE 4
www.frontiersin.org

FIGURE 4. Principal coordinate analysis (PCA) of 466 cultivated mungbean genotypes. Color-coded according to membership (based on >90% identity) to sub-populations identified from structure analysis; sub-population 1 (color-coded red), sub-population 2 (color-coded yellow), sub-population 3 (color-coded green), and sub-population 4 (color-coded purple).

Genetic Diversity between Sub-populations

The genome-wide genetic differentiation between the four contrasting mungbean sub-populations identified in structure were calculated using fixation index (FST) using PopGenome. Sub-populations 1 and 3 were the most closely related with an overall FST value of 0.42, while sub-populations 1 and 2 show the highest degree of differentiation, with an FST value of 0.57 (Table 2). Sub-population 1 had uniform green seed coats, in contrast to sub-population 2 which had a wide variation of seed coat colors. Sub-populations 1 and 3 however, shared similar characteristics with many accessions originating from Southern Asia and uniform seed color.

TABLE 2
www.frontiersin.org

TABLE 2. Genome-wide genetic differentiation (FST) between cultivated mungbean sub-populations.

Genome-Wide Association Study of Seed Coat Color QTL

TASSEL v5.1.0 was used to conduct a pilot genome-wide association mapping (GWAS) for seed coat color to demonstrate the effectiveness of the diversity panel for trait dissection. Seed coat color was chosen because it’s an oligogenic trait which does not change based on the environment the plant is grown and is economically important to the mungbean industry. Using the MLM model, nine SNPs were identified as significantly associated with seed color based on P-value < 9.66E-06 (Bonferroni correction). These SNPs were located in five distinct genomic regions distributed across chromosomes 3, 4, 5, and 7 (Supplementary Figure S5 and Supplementary Table S3). Five significant SNPs, including the most highly significant SNP overall, clustered within an interval of 22 kb on chromosome 4 between positions 17,668,384 and 17,690,573. Identified within this region VrMYB113 is the homolog of the Arabidopsis gene MYB113 involved in anthocyanin biosynthesis (Gonzalez et al., 2008). Vrsf3′h1 is the homolog of a previously identified gene (sf3h1) controlling seed coat color through flavonoid 3′-hydroxylase in soybean (Toda et al., 2012) associated with a significant SNP on chromosome 5 at position 32413093. The most significant marker (6160927|F| 0–16:A > G-16:A > G) on chromosome 4 position 17679978 had a 97% association with lighter colored seed coats (green/yellow) on allele “1,” while allele “0” had a 91% association with darker pigmentation (black/speckled) (Supplementary Table S4).

Discussion

The replacement of traditional and local crops with elite varieties harboring superior agronomic traits has led to increased yields but also the gradual erosion of genetic diversity of cultivated varieties. Globally, plant breeders are addressing the threat to cultivated crops with narrow genetic diversity by establishing large collections of genetically diverse germplasm. In this study, we investigated the application of genome-wide SNP markers to analyze the genetic diversity of a large, diverse mungbean germplasm panel. The markers generated from this germplasm panel provide a new resource to conduct high-resolution analysis of genetic diversity, population structure, LD and the capacity to identify genes controlling important agronomic traits. Additionally, this is the first high-resolution quantification of LD decay in mungbeans, defining the extent of LD within and between cultivated and wild mungbeans. The genetic diversity analysis, population structure and LD analysis provide the foundation that can be used to broaden the genetic base of mungbean breeding material. The genome-wide association study provides an example of how the data can be used to identify genomic regions responsible for phenotypic traits. SNP markers provide a level of resolution to breeding programs far beyond traditionally used methods which relied solely on passport data such as geographical origin and pedigrees (Brown, 1989) or genetic markers and quantitative phenotypic data to conduct cluster analysis of core collections (Bretting and Widrlechner, 1995). Developing effective, informed strategies for the utilization and management of germplasm collections is critical to mine the ready available diversity in mungbean (Fernandez et al., 1988). Application of this resource as a breeding tool has the potential to transform the improvement of this globally significant yet orphan crop through informed trait introgression from exotic germplasm and wild species using marker assisted breeding.

Genetic Diversity of Cultivated Mungbean

The domestication syndrome, resulting from restricting the number of elite varieties used in breeding under selection for key traits such as larger grain size, has come at the expense of diminishing overall genetic diversity (Gepts, 2010). Low genetic diversity is impeding the rate of genetic gain that can be made in breeding programs through limiting the number of alleles available in breeding populations, severely restricting the ability of breeders to continue developing improved resistance and tolerance to biotic and abiotic stressors. Broadening the genetic base of mungbean and incorporating exotic alleles is essential to developing agile breeding programs that can respond to new threats and challenges faced by the crop (Nair et al., 2012). Over the last decade, limited research has been conducted to investigate the degree of genetic diversity within and between cultivated and wild mungbean. The first large-scale analysis of cultivated and wild mungbean germplasm using molecular markers was conducted by Sangiri et al. (2007) who analyzed the domestication of mungbean. Our study represents the first extensive mungbean germplasm diversity analysis using high-density SNP markers.

Highly informative PIC values as defined by Botstein et al. (1980) are values equal to or greater than 0.5 when considering multi-allelic markers whose values range from 0 to 1. PIC values for bi-allelic SNP markers range from 0 to 0.5, therefore we have regarded PIC values greater than or equal to 0.25 as highly informative. Within the cultivated population 34% of the SNPs had a PIC value greater than or equal to 0.25 compared to the wild population, which had 56%. The high PIC value derived from the wild population is consistent with our expectations that we would see a greater proportion of highly polymorphic markers in the wild population due to the selective breeding seen in the cultivated population.

The clear differentiation between cultivated and wild mungbean gene pools, as demonstrated in the PCA analysis (Supplementary Figure S4), was also reported by Sangiri et al. (2007), who noted close to double the gene diversity in the wild population in comparison to cultivated mungbeans and clear genetic differentiation among the cultivated accessions. Sangiri et al. (2007) observed that approximately 50% of the genetic variation present in the wild mungbean gene pool was found in the cultivated germplasm. In contrast, other cultivated cereals have been observed to contain only ∼30% of the genetic diversity present in wild species, indicating that mungbeans have experienced a weaker genetic bottle neck than that of the cereals, reflecting the difference in the domestication process of legumes compared with cereals (Buckler et al., 2001; Zhu et al., 2007).

LD in Mungbean Is Comparable to Closely Related Species

The number and density of markers required for an association mapping analysis is determined by the distance over which LD decays. The LD patterns of mungbean reflect its long history of domestication (Fuller, 2007) and as a self-pollinated species the extent of genome-wide recombination is expected to be less than that observed in cross pollinated species (Flint-Garcia et al., 2003). The r2 of cultivated mungbean decreased to half its maximum value at ∼100 kb compared to that of the wild species which decreased by ∼60 kb (Figure 2). Wild mungbean has retained a higher degree of allelic diversity providing an important source of material for increasing the genetic diversity of the cultivated gene pool.

Studies in closely related species report that LD largely decays by ∼150 kb in cultivated soybean; ∼75 kb in wild soybean (Lam et al., 2010) and in chickpea between 450 and 550 kb (Bajaj et al., 2015). In contrast, in Medicago truncatula, a leguminous plant used in genomic studies the LD decayed rapidly, dropping too approximately half of its initial value within ∼3 kb (Branca et al., 2011) similar to the model speices Arabidopsis thaliana: 3–4 kb (Kim et al., 2007). Cultivated and wild rice reported the highest variation between the highly cultivated varieties O. japonica at ∼200 kb and O. indica ∼65 kb in contrast to wild varieties O. rufipogon and O. nivara which exhibit rapid decay by ∼10 kb (Xu et al., 2011), similar to sorghum: improved inbreds ∼19.7 kb and land races ∼10.3 kb (Mace et al., 2013). These studies show the major influence domestication has had on changing genome dynamics and combined with PIC data, highlights the importance wild accessions and genetically diverse populations will have on providing access to new exotic alleles.

High-Resolution Association Mapping Pilot Study

QTL (quantitative trait loci) are identified through the establishment of association between genomic marker data and traits of interest. Previous studies revealed the genetic factors controlling important agronomic traits in mungbean using biparental populations such as, major QTLs for hard-seededness and seed weight (Fatokun et al., 1992; Maughan et al., 1996; Humphry et al., 2005); powdery mildew resistance (Young et al., 1993; Chaitieng et al., 2002; Humphry et al., 2003; Kasettranan et al., 2010); yellow mosaic Indian virus resistance (Chen et al., 2012; Kitsanachandee et al., 2013); bruchid resistance (Young et al., 1992; Mei et al., 2009); Cercospora leaf spot resistance (Chankaew et al., 2011). Due to the limited number of recombination events (Balasubramanian et al., 2009), QTLs were commonly mapped to wide-ranging intervals extending over a number of centiMorgans (cM), usually megabases (Mb) long in physical distance, potentially containing 100s of candidate genes. Thus, the understanding of specific genes controlling agronomic traits is still restricted and further fine-mapping is often required to identify the underlying genes involved.

The structure of our population, which captured vast historical recombination accumulated during mungbean cultivation, combined with the high density of markers genome-wide overcome barriers seen in previous studies. The GWAS performed in this study (Figure 5) is an example of how the features of this data set can provide high resolution mapping opportunities. A Nested Association Mapping (NAM) population in mungbean, currently being developed by the Queensland mungbean improvement team, will provide a powerful complementary population to the diversity panel described here. The structure of the mungbean NAM population encompasses 26 of the most genetically and phenotypically diverse accessions, backcrossed to one elite line adapted to the local production (Supplementary Figure S5). environment. Robust precise phenotyping and genotying of the NAM population will push mungbean breeding years ahead of its time accelerating genome research and molecular breeding.

FIGURE 5
www.frontiersin.org

FIGURE 5. Genome-wide association mapping (GWAS) results for seed coat color in mungbean. Nine SNPs identified as significantly associated with seed color located in five distinct genomic regions distributed across chromosomes 3, 4, 5, and 7. VrMYB113 is the homolog of Arabidopsis gene MYB113 located on chromosome 4 between position 17,668,384 and 17,690,573. Vrsf3′h1 is the homolog of soybean gene sf3′h1 located on chromosome 5 position 32,413,093.

Author Contributions

CD, DJ, and EM conceived and designed the experiments. TN collected the data. TN, EM, and YT analyzed data. TN, EM, and YT wrote the manuscript. SM, BW, DJ, and EM revised the manuscript. All authors read and approved the final manuscript.

Funding

This work was supported by the Queensland Government’s, Tropical Pulses for Queensland (TPFQ) initiative (2013000320) and an Australian Mungbean Association (AMA) Ph.D. scholarship (2017000885).

Conflict of Interest Statement

The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.

Acknowledgments

The authors acknowledge the Centre for Tropical Crops and Biocommodities, Queensland University of Technology, Brisbane, QLD, Australia and the Australian Mungbean Association for providing funding to complete this work under the Tropical Pulses for Queensland (TPFQ) initiative and the AMA Ph.D. scholarship. They would also like to thank the staff at the DAF Hermitage Research Facility, Warwick, QLD, Australia for their valuable support and contribution throughout the entire project and Prof. Robert Lawn from James Cook University in Townsville, QLD for providing the wild Australian mungbean accessions.

Supplementary Material

The Supplementary Material for this article can be found online at: https://www.frontiersin.org/articles/10.3389/fpls.2017.02102/full#supplementary-material

Footnotes

  1. ^ http://www.diversityarrays.com
  2. ^ http://www.diversityarrays.com

References

Abdurakhmonov, I. Y., and Abdukarimov, A. (2008). Application of association mapping to understanding the genetic diversity of plant germplasm resources. Int. J. Plant Genomics 2008:574927. doi: 10.1155/2008/574927

PubMed Abstract | CrossRef Full Text | Google Scholar

Bajaj, D., Das, S., Badoni, S., Kumar, V., Singh, M., Bansal, K. C., et al. (2015). Genome-wide high-throughput SNP discovery and genotyping for understanding natural (functional) allelic diversity and domestication patterns in wild chickpea. Sci. Rep. 5:12468. doi: 10.1038/srep12468

PubMed Abstract | CrossRef Full Text | Google Scholar

Balasubramanian, S., Schwartz, C., Singh, A., Warthmann, N., Kim, M. C., Maloof, J. N., et al. (2009). QTL mapping in new Arabidopsis thaliana advanced intercross-recombinant inbred lines. PLOS ONE 4:e4318. doi: 10.1371/journal.pone.0004318

PubMed Abstract | CrossRef Full Text | Google Scholar

Botstein, D., White, R. L., Skolnick, M., and Davis, R. W. (1980). Construction of a genetic-linkage map in man using restriction fragment length polymorphisms. Am. J. Hum. Genet. 32, 314–331.

Google Scholar

Bradbury, P. J., Zhang, Z., Kroon, D. E., Casstevens, R. M., Ramdoss, Y., and Buckler, E. S. (2007). TASSELL software for association mapping of complex traits in diverse samples. Bioinformatics 23, 2633–2635. doi: 10.1371/journal.pgen.0030004.4

PubMed Abstract | CrossRef Full Text | Google Scholar

Branca, A., Paape, T. D., Zhou, P., Briskine, R., Farmer, A. D., Mudge, J., et al. (2011). Whole-genome nucleotide diversity, recombination, and linkage disequilibrium in the model legume Medicago truncatula. Proc. Natl. Acad. Sci. U.S.A. 108, 864–870. doi: 10.1073/pnas.1104032108

PubMed Abstract | CrossRef Full Text | Google Scholar

Bretting, P. K., and Widrlechner, M. P. (1995). Genetic Markers and Plant Genetic Resource Management. New York, NY: John Wiley & Sons, 11–86.

Google Scholar

Brown, A. H. D. (1989). Core collections - a practical approach to genetic-resources management. Genome 31, 818–824. doi: 10.1139/g89-144

CrossRef Full Text | Google Scholar

Buckler, E. S. T., Thornsberry, J. M., and Kresovich, S. (2001). Molecular diversity, structure and domestication of grasses. Genet. Res. 77, 213–218. doi: 10.1017/S0016672301005158

CrossRef Full Text | Google Scholar

Chaitieng, B., Kaga, A., Han, O. K., Wang, X. W., Wongkaew, S., Laosuwan, P., et al. (2002). Mapping a new source of resistance to powdery mildew in mungbean. Plant Breed. 121, 521–525. doi: 10.1046/j.1439-0523.2002.00751.x

CrossRef Full Text | Google Scholar

Chankaew, S., Somta, P., Sorajjapinun, W., and Srinives, P. (2011). Quantitative trait loci mapping of Cercospora leaf spot resistance in mungbean, Vigna radiata (L.) Wilczek. Mol. Breed. 28, 255–264. doi: 10.1007/s11032-010-9478-1

CrossRef Full Text | Google Scholar

Chen, H.-M., Ku, H.-M., Schafleitner, R., Bains, T. S., George Kuo, C., Liu, C.-A., et al. (2012). The major quantitative trait locus for mungbean yellow mosaic Indian virus resistance is tightly linked in repulsion phase to the major bruchid resistance locus in a cross between mungbean [Vigna radiata (L.) Wilczek] and its wild relative Vigna radiata ssp. sublobata. Euphytica 192, 205–216. doi: 10.1007/s10681-012-0831-9

CrossRef Full Text | Google Scholar

Day, L. (2013). Proteins from land plants - Potential resources for human nutrition and food security. Trends Food Sci. Technol. 32, 25–42. doi: 10.1016/j.tifs.2013.05.005

PubMed Abstract | CrossRef Full Text | Google Scholar

Ellis, R. P., Forster, B. P., Robinson, D., Handley, L. L., Gordon, D. C., Russell, J. R., et al. (2000). Wild barley: a source of genes for crop improvement in the 21st century? J. Exp. Bot. 51, 9–17. doi: 10.1093/jexbot/51.342.9

PubMed Abstract | CrossRef Full Text | Google Scholar

Falush, D., Stephens, M., and Pritchard, J. K. (2007). Inference of population structure using multilocus genotype data: dominant markers and null alleles. Mol. Ecol. Notes 7, 574–578. doi: 10.1111/j.1471-8286.2007.01758.x

PubMed Abstract | CrossRef Full Text | Google Scholar

Fatokun, C. A., Menancio-Hautea, D. I., Danesh, D., and Young, N. D. (1992). Evidence for orthologous seed weight genes in cowpea and mung bean based on RFLP mapping. Genetics 132, 841–846.

PubMed Abstract | Google Scholar

Fernandez, G. C. J., Shanmugasundaram, S., and McLean, B. T. (1988). “The AVRDC mungbean improvement program: the past, present and future,” in Proceedings of the Second International Symposium, Bangkok, 58–70.

Google Scholar

Flint-Garcia, S. A., Thornsberry, J. M., and Buckler, E. S. T. (2003). Structure of linkage disequilibrium in plants. Annu. Rev. Plant Biol. 54, 357–374. doi: 10.1146/annurev.arplant.54.031902.134907

PubMed Abstract | CrossRef Full Text | Google Scholar

Fuller, D. Q. (2007). Contrasting patterns in crop domestication and domestication rates: recent archaeobotanical insights from the Old World. Ann. Bot. 100, 903–924. doi: 10.1093/aob/mcm048

PubMed Abstract | CrossRef Full Text | Google Scholar

Gepts, P. (2010). Crop domestication as a long-term selection experiment. Plant Breed. Rev. 24(Pt 2), 1–44. doi: 10.1093/jxb/erw006

PubMed Abstract | CrossRef Full Text | Google Scholar

Gonzalez, A., Zhao, M., Leavitt, J. M., and Lloyd, A. M. (2008). Regulation of the anthocyanin biosynthetic pathway by the TTG1/bHLH/Myb transcriptional complex in Arabidopsis seedlings. Plant J. 53, 814–827. doi: 10.1111/j.1365-313X.2007.03373.x

PubMed Abstract | CrossRef Full Text | Google Scholar

Gupta, P. K., Rustgi, S., and Kulwal, P. L. (2005). Linkage disequilibrium and association studies in higher plants: present status and future prospects. Plant Mol. Biol. 57, 461–485. doi: 10.1007/s11103-005-0257-z

PubMed Abstract | CrossRef Full Text | Google Scholar

Humphry, E., Konduri, V., Lambrides, J., Magner, T., McIntyre, L., Aitken, B., et al. (2002). Development of a mungbean (Vigna radiata) RFLP linkage map and its comparison with lablab (Lablab purpureus) reveals a high level of colinearity between the two genomes. Theor. Appl. Genet. 105, 160–166. doi: 10.1007/s00122-002-0909-1

PubMed Abstract | CrossRef Full Text | Google Scholar

Humphry, M. E., Lambrides, C. J., Chapman, S. C., Aitken, E. A. B., Imrie, B. C., Lawn, R. J., et al. (2005). Relationships between hard-seededness and seed weight in mungbean (Vigna radiata) assessed by QTL analysis. Plant Breed. 124, 292–298. doi: 10.1111/j.1439-0523.2005.01084.x

CrossRef Full Text | Google Scholar

Humphry, M. E., Magner, T., McIntyre, C. L., Aitken, E. A., and Liu, C. J. (2003). Identification of a major locus conferring resistance to powdery mildew (Erysiphe polygoni DC) in mungbean (Vigna radiata L. Wilczek) by QTL analysis. Genome 46, 738–744. doi: 10.1139/g03-057

PubMed Abstract | CrossRef Full Text | Google Scholar

Isemura, T., Kaga, A., Tabata, S., Somta, P., Srinives, P., Shimizu, T., et al. (2012). Construction of a genetic linkage map and genetic analysis of domestication related traits in mungbean (Vigna radiata). PLOS ONE 7:e41304. doi: 10.1371/journal.pone.0041304

PubMed Abstract | CrossRef Full Text | Google Scholar

Jordan, D. R., Mace, E. S., Cruickshank, A. W., Hunt, C. H., and Henzell, R. G. (2011). Exploring and exploiting genetic variation from unadapted sorghum germplasm in a breeding program. Crop Sci. 51, 1444–1457. doi: 10.2135/cropsci2010.06.0326

CrossRef Full Text | Google Scholar

Kang, Y. J., Kim, S. K., Kim, M. Y., Lestari, P., Kim, K. H., Ha, B. K., et al. (2014). Genome sequence of mungbean and insights into evolution within Vigna species. Nat. Commun. 5:5443. doi: 10.1038/ncomms6443

PubMed Abstract | CrossRef Full Text | Google Scholar

Kasettranan, W., Somta, P., and Srinives, P. (2010). Mapping of quantitative trait loci controlling powdery mildew resistance in Mungbean (Vigna radiata (L.) Wilczek). J. Crop Sci. Biotechnol. 13, 155–161. doi: 10.1007/s12892-010-0052-z

CrossRef Full Text | Google Scholar

Kim, S., Plagnol, V., Hu, T. T., Toomajian, C., Clark, R. M., Ossowski, S., et al. (2007). Recombination and linkage disequilibrium in Arabidopsis thaliana. Nat. Genet. 39, 1151–1155. doi: 10.1038/ng2115

PubMed Abstract | CrossRef Full Text | Google Scholar

Kim, S. K., Nair, R. M., Lee, J., and Lee, S. H. (2015). Genomic resources in mungbean for future breeding programs. Front. Plant Sci. 6:626. doi: 10.3389/fpls.2015.00626

PubMed Abstract | CrossRef Full Text | Google Scholar

Kitsanachandee, R., Somta, P., Chatchawankanphanich, O., Akhtar, K. P., Shah, T. M., Nair, R. M., et al. (2013). Detection of quantitative trait loci for mungbean yellow mosaic India virus (MYMIV) resistance in mungbean (Vigna radiata (L.) Wilczek) in India and Pakistan. Breed. Sci. 63, 367–373. doi: 10.1270/jsbbs.63.367

PubMed Abstract | CrossRef Full Text | Google Scholar

Lakhanpaul, S., Chadha, S., and Bhat, K. V. (2000). Random amplified polymorphic DNA (RAPD) analysis in Indian mung bean (Vigna radiata (L.) Wilczek) cultivars. Genetica 109, 227–234. doi: 10.1023/A:1017511918528

PubMed Abstract | CrossRef Full Text | Google Scholar

Lam, H. M., Xu, X., Liu, X., Chen, W., Yang, G., Wong, F. L., et al. (2010). Resequencing of 31 wild and cultivated soybean genomes identifies patterns of genetic diversity and selection. Nat. Genet. 42, 1053–1059. doi: 10.1038/ng.715

PubMed Abstract | CrossRef Full Text | Google Scholar

Lambrides, C. J., James, A. T., Lawn, R. J., and Williams, R. W. (1999). Cross fertility of Australian accessions of wild mungbean (Vigna radiata ssp. sublobata) with Green Gram (V. radiata ssp. radiata) and black gram (V. mungo). Aust. J. Bot. 47, 601–610. doi: 10.1071/BT97068

CrossRef Full Text | Google Scholar

Lambrides, C. J., Lawn, R. J., Godwin, I. D., Manners, J., and Imrie, B. C. (2000). Two genetic linkage maps of mungbean using RFLP and RAPD markers. Aust. J. Agric. Res. 51, 415–425. doi: 10.1071/Ar99052

PubMed Abstract | CrossRef Full Text | Google Scholar

Mace, E. S., Tai, S., Gilding, E. K., Li, Y., Prentis, P. J., Bian, L., et al. (2013). Whole-genome sequencing reveals untapped genetic potential in Africa’s indigenous cereal crop sorghum. Nat. Commun. 4:2320. doi: 10.1038/ncomms3320

PubMed Abstract | CrossRef Full Text | Google Scholar

Maughan, P. J., Maroof, M. A., and Buss, G. R. (1996). Molecular-marker analysis of seed-weight: genomic locations, gene action, and evidence for orthologous evolution among three legume species. Theor. Appl. Genet. 93, 574–579. doi: 10.1007/BF00417950

PubMed Abstract | CrossRef Full Text | Google Scholar

Mei, L., Cheng, X. Z., Wang, S. H., Wang, L. X., Liu, C. Y., Sun, L., et al. (2009). Relationship between bruchid resistance and seed mass in mungbean based on QTL analysis. Genome 52, 589–596. doi: 10.1139/G09-031

PubMed Abstract | CrossRef Full Text | Google Scholar

Nair, R. M., Schafleitner, R., Kenyon, L., Srinivasan, R., Easdown, W., Ebert, A. W., et al. (2012). Genetic improvement of mungbean. SABRAO J. Breed. Genet. 44, 177–190.

Google Scholar

Pandiyan, M., Ramamoorthi, N., Ganesh, S. K., Jebaraj, S., Pagarajan, P., and Balasubramanian, P. (2008). Research article broadening the genetic base and introgression of MYMV resistance and yield improvement through unexplored genes from wild relatives in mungbean. Plant Mutat. Rep. 2, 33–43.

Google Scholar

Parida, A., Raina, S. N., and Narayan, R. K. J. (1990). Quantitative DNA variation between and within chromosome complements of Vigna species (Fabaceae). Genetica 82, 125–133. doi: 10.1007/Bf00124642

CrossRef Full Text | Google Scholar

Perrier, X., and Jacquemoud-Collet, J. P. (2006). DARwin Software. Available at: http://darwin.cirad.fr/

Google Scholar

Pfeifer, B., Wittelsburger, U., Ramos-Onsins, S. E., and Lercher, M. J. (2014). PopGenome: an efficient Swiss army knife for population genomic analyses in R. Mol. Biol. Evol. 31, 1929–1936. doi: 10.1093/molbev/msu136

PubMed Abstract | CrossRef Full Text | Google Scholar

Rebetzke, G. J., and Lawn, R. J. (2006a). Adaptive responses of wild mungbean (Vigna radiata ssp sublobata) to photo-thermal environment. I. Phenology. Aust. J. Agric. Res. 57, 917–928. doi: 10.1071/Ar05357

CrossRef Full Text | Google Scholar

Rebetzke, G. J., and Lawn, R. J. (2006b). Adaptive responses of wild mungbean (Vigna radiata ssp. sublobata) to photo-thermal environment. II. Growth, biomass, and seed yield. Aust. J. Agric. Res. 57, 929–937. doi: 10.1071/Ar05377

CrossRef Full Text | Google Scholar

Rebetzke, G. J., and Lawn, R. J. (2006c). Root and shoot attributes of indigenous perennial accessions of the wild mungbean (Vigna radiata ssp. sublobata). Aust. J. Agric. Res. 57, 791–799. doi: 10.1071/Ar05363

CrossRef Full Text | Google Scholar

Sangiri, C., Kaga, A., Tomooka, N., Vaughan, D., and Srinives, P. (2007). Genetic diversity of the mungbean (Vigna radiata, Leguminosae) genepool on the basis of microsatellite analysis. Aust. J. Bot. 55, 837–847. doi: 10.1071/Bt07105

CrossRef Full Text | Google Scholar

Santalla, M., Power, J. B., and Davey, M. R. (1998). Genetic diversity in mung bean germplasm revealed by RAPD markers. Plant Breed. 117, 473–478. doi: 10.1111/j.1439-0523.1998.tb01976.x

CrossRef Full Text | Google Scholar

Saravanakumar, P., Kaga, A., Tomooka, N., and Vaughan, D. A. (2004). AFLP and RAPD analyses of intra- and interspecific variation in some Vigna subgenus Ceratotropis (Leguminosae) species. Aust. J. Bot. 52, 417–424. doi: 10.1071/Bt03091

CrossRef Full Text | Google Scholar

Tao, Y., Jiang, L., Liu, Q., Zhang, Y., Zhang, R., Ingvardsen, C. R., et al. (2013). Combined linkage and association mapping reveals candidates for Scmv1, a major locus involved in resistance to sugarcane mosaic virus (SCMV) in maize. BMC Plant Biol. 13:162. doi: 10.1186/1471-2229-13-162

PubMed Abstract | CrossRef Full Text | Google Scholar

Toda, K., Kuroiwa, H., Senthil, K., Shimada, N., Aoki, T., Ayabe, S., et al. (2012). The soybean F3’H protein is localized to the tonoplast in the seed coat hilum. Planta 236, 79–89. doi: 10.1007/s00425-012-1590-5

PubMed Abstract | CrossRef Full Text | Google Scholar

Turner, S. D. (2014). qqman: an R package for visualizing GWAS results using Q-Q and manhattan plots. bioRxiv bioRxiv:005165. doi: 10.1101/005165

CrossRef Full Text | Google Scholar

Weir, B. S. (1990). Genetic Data Analysis. Methods for Discrete Population Genetic Data. Sunderland MA: Sinauer Associates.

Google Scholar

Xu, X., Liu, X., Ge, S., Jensen, J. D., Hu, F., Li, X., et al. (2011). Resequencing 50 accessions of cultivated and wild rice yields markers for identifying agronomically important genes. Nat. Biotechnol. 30, 105–111. doi: 10.1038/nbt.2050

PubMed Abstract | CrossRef Full Text | Google Scholar

Young, N. D., Danesh, D., Menancio-Hautea, D., and Kumar, L. (1993). Mapping oligogenic resistance to powdery mildew in mungbean with RFLPs. Theor. Appl. Genet. 87, 243–249. doi: 10.1007/BF00223772

PubMed Abstract | CrossRef Full Text | Google Scholar

Young, N. D., Kumar, L., Menancio-Hautea, D., Danesh, D., Talekar, N. S., Shanmugasundarum, S., et al. (1992). RFLP mapping of a major bruchid resistance gene in mungbean (Vigna radiata, L. Wilczek). Theor. Appl. Genet. 84, 839–844. doi: 10.1007/BF00227394

PubMed Abstract | CrossRef Full Text | Google Scholar

Zhu, Q., Zheng, X., Luo, J., Gaut, B. S., and Ge, S. (2007). Multilocus analysis of nucleotide variation of Oryza sativa and its wild relatives: severe bottleneck during domestication of rice. Mol. Biol. Evol. 24, 875–888. doi: 10.1093/molbev/msm005

PubMed Abstract | CrossRef Full Text | Google Scholar

Keywords: mungbean, Vigna radiata, genetic diversity, linkage disequilibrium, population structure, genome-wide association mapping, SNP

Citation: Noble TJ, Tao Y, Mace ES, Williams B, Jordan DR, Douglas CA and Mundree SG (2018) Characterization of Linkage Disequilibrium and Population Structure in a Mungbean Diversity Panel. Front. Plant Sci. 8:2102. doi: 10.3389/fpls.2017.02102

Received: 29 August 2017; Accepted: 27 November 2017;
Published: 12 January 2018.

Edited by:

Roberto Papa, Università Politecnica delle Marche, Italy

Reviewed by:

Andrea Ariani, University of California, Davis, United States
Giovanna Attene, University of Sassari, Italy

Copyright © 2018 Noble, Tao, Mace, Williams, Jordan, Douglas and Mundree. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.

*Correspondence: Yongfu Tao, y.tao1@uq.edu.au Sagadevan G. Mundree, sagadevan.mundree@qut.edu.au Colin A. Douglas, col.douglas@daf.qld.gov.au

Disclaimer: All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article or claim that may be made by its manufacturer is not guaranteed or endorsed by the publisher.