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全基因组关联研究(GWAS)。

Genome-Wide Association Studies (GWAS).

机构信息

Soybean Research Institute, Nanjing Agricultural University, Nanjing, China.

出版信息

Methods Mol Biol. 2023;2638:123-146. doi: 10.1007/978-1-0716-3024-2_9.

Abstract

Most of the breeding targets are quantitative traits. In exploring the quantitative trait locus (QTL) system of a trait, linkage mapping was established using sparse polymerase chain reaction (PCR) markers. With the genome-wide sequencing technology advanced, genome-wide association study (GWAS) was developed for natural (germplasm) populations using dense genomic markers, which facilitates the identification of the complete QTL system with their multiple alleles on genomic locations. GWAS makes use of the linkage disequilibrium (LD) due to historical saturate recombination and high-density genomic markers to detect QTLs through statistical test for the association between molecular markers and phenotypes. However, due to inbreeding and mixture of source populations, the germplasm population often has complex and unknown structure, which leads to false positives/negatives in GWAS. Various GWAS methods have been proposed to reduce false positives/negatives, including those of the general linear model and the mixed linear model, which focused mainly on finding a handful of major QTLs under single-locus model for major gene cloning and could not detect directly the multiple alleles using bi-allelic single-nucleotide polymorphism (SNP) marker. As a relatively thorough detection of QTLs with their multiple alleles is required for germplasm population, the restricted two-stage multi-locus multi-allele GWAS (RTM-GWAS) procedure was proposed for identifying the QTL system with varying multiple alleles. From the RTM-GWAS results, a QTL-allele matrix is constructed as a compact form of the population genetic constitution, which can be further used for crop genetic and breeding studies, including major gene mining, population evolution, and breeding by genetic design.

摘要

大多数的育种目标是数量性状。在探索一个性状的数量性状基因座(QTL)系统时,使用稀疏的聚合酶链反应(PCR)标记建立了连锁图谱。随着全基因组测序技术的进步,利用密集的基因组标记对自然(种质)群体进行了全基因组关联研究(GWAS),这有助于识别基因组位置上具有多个等位基因的完整 QTL 系统。GWAS 利用由于历史上饱和重组和高密度基因组标记导致的连锁不平衡(LD),通过对分子标记与表型之间的关联进行统计检验来检测 QTL。然而,由于近亲繁殖和来源群体的混合,种质群体通常具有复杂和未知的结构,这导致 GWAS 中出现假阳性/假阴性。已经提出了各种 GWAS 方法来减少假阳性/假阴性,包括一般线性模型和混合线性模型,这些方法主要集中在单基因座模型下寻找少数主要 QTL 以进行主要基因克隆,并且不能直接使用双等位单核苷酸多态性(SNP)标记检测多个等位基因。由于需要对种质群体进行相对彻底的多个等位基因 QTL 检测,因此提出了受限两阶段多基因座多等位基因 GWAS(RTM-GWAS)程序,用于识别具有不同多个等位基因的 QTL 系统。从 RTM-GWAS 结果中,构建了一个 QTL-allele 矩阵,作为群体遗传构成的紧凑形式,可进一步用于作物遗传和育种研究,包括主要基因挖掘、群体进化和遗传设计的育种。

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