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Cold Tolerance SNPs and Candidate Gene Mining in the Soybean Germination Stage Based on Genome-wide Association Analysis

Overview
Publisher Springer
Specialty Genetics
Date 2024 Jul 8
PMID 38976061
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Abstract

Three QTLs associated with low-temperature tolerance were identified by genome-wide association analysis, and 15 candidate genes were identified by haplotype analysis and gene expression analyses. Low temperature is a critical factor affecting the geographical distribution, growth, development, and yield of soybeans, with cold stress during seed germination leading to substantial productivity loss. In this study, an association panel comprising 260 soybean accessions was evaluated for four germination traits and four cold tolerance index traits, revealing extensive variation in cold tolerance. Genome-wide association study (GWAS) identified 10 quantitative trait nucleotides (QTNs) associated with cold tolerance, utilizing 30,799 single nucleotide polymorphisms (SNPs) and four GWAS models. Linkage disequilibrium (LD) analysis positioned these QTNs within three cold-tolerance quantitative trait loci (QTL) and, with QTL19-1, was positioned by three multi-locus models, underscoring its importance as a key QTL. Integrative haplotype analysis, supplemented by transcriptome analysis, uncovered 15 candidate genes. The haplotypes within the genes Glyma.18G044200, Glyma.18G044300, Glyma.18G044900, Glyma.18G045100, Glyma.19G222500, and Glyma.19G222600 exhibited significant phenotypic variations, with differential expression in materials with varying cold tolerance. The QTNs and candidate genes identified in this study offer substantial potential for marker-assisted selection and gene editing in breeding cold-tolerant soybeans, providing valuable insights into the genetic mechanisms underlying cold tolerance during soybean germination.

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References
1.
Benko P, Gemes K, Feher A . Polyamine Oxidase-Generated Reactive Oxygen Species in Plant Development and Adaptation: The Polyamine Oxidase-NADPH Oxidase Nexus. Antioxidants (Basel). 2022; 11(12). PMC: 9774701. DOI: 10.3390/antiox11122488. View

2.
Bradbury P, Zhang Z, Kroon D, Casstevens T, Ramdoss Y, Buckler E . TASSEL: software for association mapping of complex traits in diverse samples. Bioinformatics. 2007; 23(19):2633-5. DOI: 10.1093/bioinformatics/btm308. View

3.
Burroughs A, Allen K, Dunaway-Mariano D, Aravind L . Evolutionary genomics of the HAD superfamily: understanding the structural adaptations and catalytic diversity in a superfamily of phosphoesterases and allied enzymes. J Mol Biol. 2006; 361(5):1003-34. DOI: 10.1016/j.jmb.2006.06.049. View

4.
Cai W, Ma J, Guo J, Zhang L . Function of ROC4 in the efficient repair of photodamaged photosystem II in Arabidopsis. Photochem Photobiol. 2008; 84(6):1343-8. DOI: 10.1111/j.1751-1097.2008.00448.x. View

5.
Diao P, Chen C, Zhang Y, Meng Q, Lv W, Ma N . The role of NAC transcription factor in plant cold response. Plant Signal Behav. 2020; 15(9):1785668. PMC: 8550289. DOI: 10.1080/15592324.2020.1785668. View