Ashish Kumar, Yogesh Dashrath Naik, Vedant Gautam, Sunanda Patil, Vinod Valluri, Sonal Channale, Jayant Bhatt, Stuti Sharma, R. S. Ramakrishnan, Radheshyam Sharma, Himabindu Kudapa, Rebecca S. Zwart, Somashekhar M. Punnuri, Rajeev K. Varshney, Mahendar Thudi
{"title":"Genome‐wide association mapping reveals novel genes and genomic regions controlling root‐lesion nematode resistance in chickpea mini core collection","authors":"Ashish Kumar, Yogesh Dashrath Naik, Vedant Gautam, Sunanda Patil, Vinod Valluri, Sonal Channale, Jayant Bhatt, Stuti Sharma, R. S. Ramakrishnan, Radheshyam Sharma, Himabindu Kudapa, Rebecca S. Zwart, Somashekhar M. Punnuri, Rajeev K. Varshney, Mahendar Thudi","doi":"10.1002/tpg2.20508","DOIUrl":null,"url":null,"abstract":"Root‐lesion nematodes (RLN) pose a significant threat to chickpea (<jats:italic>Cicer arietinum</jats:italic> L.) by damaging the root system and causing up to 25% economic losses due to reduced yield. Worldwide commercially grown chickpea varieties lack significant genetic resistance to RLN, necessitating the identification of genetic variants contributing to natural resistance. This study identifies genomic loci responsible for resistance to the RLN, <jats:italic>Pratylenchus thornei</jats:italic> Sher & Allen, in chickpea by utilizing high‐quality single nucleotide polymorphisms from whole‐genome sequencing data of 202 chickpea accessions. Phenotypic evaluations of the genetically diverse set of chickpea accessions in India and Australia revealed a wide range of responses from resistant to susceptible. Genome‐wide association studies (GWAS) employing Fixed and Random Model Circulating Probability Unification (FarmCPU) and Bayesian‐Information and Linkage‐Disequilibrium Iteratively Nested Keyway (BLINK) models identified 44 marker‐trait associations distributed across all chromosomes except Ca1. Crucially, genomic regions on Ca2 and Ca5 consistently display significant associations across locations. Of 25 candidate genes identified, five genes were putatively involved in RLN resistance response (glucose‐6‐phosphate dehydrogenase, heat shock proteins, MYB‐like DNA‐binding protein, zinc finger FYVE protein and pathogenesis‐related thaumatin‐like protein). One notably identified gene (<jats:italic>Ca_10016</jats:italic>) presents four haplotypes, where haplotypes 1–3 confer moderate susceptibility, and haplotype 4 contributes to high susceptibility to RLN. This information provides potential targets for marker development to enhance breeding for RLN resistance in chickpea. Additionally, five potential resistant genotypes (ICC3512, ICC8855, ICC5337, ICC8950, and ICC6537) to <jats:italic>P. thornei</jats:italic> were identified based on their performance at a specific location. The study's significance lies in its comprehensive approach, integrating multiple‐location phenotypic evaluations, advanced GWAS models, and functional genomics to unravel the genetic basis of <jats:italic>P. thornei</jats:italic> resistance. The identified genomic regions, candidate genes, and haplotypes offer valuable insights for breeding strategies, paving the way for developing chickpea varieties resilient to <jats:italic>P. thornei</jats:italic> attack.","PeriodicalId":501653,"journal":{"name":"The Plant Genome","volume":"62 1","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2024-09-13","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"The Plant Genome","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1002/tpg2.20508","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0
Abstract
Root‐lesion nematodes (RLN) pose a significant threat to chickpea (Cicer arietinum L.) by damaging the root system and causing up to 25% economic losses due to reduced yield. Worldwide commercially grown chickpea varieties lack significant genetic resistance to RLN, necessitating the identification of genetic variants contributing to natural resistance. This study identifies genomic loci responsible for resistance to the RLN, Pratylenchus thornei Sher & Allen, in chickpea by utilizing high‐quality single nucleotide polymorphisms from whole‐genome sequencing data of 202 chickpea accessions. Phenotypic evaluations of the genetically diverse set of chickpea accessions in India and Australia revealed a wide range of responses from resistant to susceptible. Genome‐wide association studies (GWAS) employing Fixed and Random Model Circulating Probability Unification (FarmCPU) and Bayesian‐Information and Linkage‐Disequilibrium Iteratively Nested Keyway (BLINK) models identified 44 marker‐trait associations distributed across all chromosomes except Ca1. Crucially, genomic regions on Ca2 and Ca5 consistently display significant associations across locations. Of 25 candidate genes identified, five genes were putatively involved in RLN resistance response (glucose‐6‐phosphate dehydrogenase, heat shock proteins, MYB‐like DNA‐binding protein, zinc finger FYVE protein and pathogenesis‐related thaumatin‐like protein). One notably identified gene (Ca_10016) presents four haplotypes, where haplotypes 1–3 confer moderate susceptibility, and haplotype 4 contributes to high susceptibility to RLN. This information provides potential targets for marker development to enhance breeding for RLN resistance in chickpea. Additionally, five potential resistant genotypes (ICC3512, ICC8855, ICC5337, ICC8950, and ICC6537) to P. thornei were identified based on their performance at a specific location. The study's significance lies in its comprehensive approach, integrating multiple‐location phenotypic evaluations, advanced GWAS models, and functional genomics to unravel the genetic basis of P. thornei resistance. The identified genomic regions, candidate genes, and haplotypes offer valuable insights for breeding strategies, paving the way for developing chickpea varieties resilient to P. thornei attack.