首页> 外文期刊>Theoretical and Applied Genetics: International Journal of Breeding Research and Cell Genetics >Joint linkage QTL analyses for partial resistance to Phytophthora sojae in soybean using six nested inbred populations with heterogeneous conditions.
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Joint linkage QTL analyses for partial resistance to Phytophthora sojae in soybean using six nested inbred populations with heterogeneous conditions.

机译:使用六个具有不同条件的嵌套近交种群,对大豆疫霉菌的部分抗性进行联合连锁QTL分析。

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摘要

Partial resistance to Phytophthora sojae in soybean is controlled by multiple quantitative trait loci (QTL). With traditional QTL mapping approaches, power to detect such QTL, frequently of small effect, can be limited by population size. Joint linkage QTL analysis of nested recombinant inbred line (RIL) populations provides improved power to detect QTL through increased population size, recombination, and allelic diversity. However, uniform development and phenotyping of multiple RIL populations can prove difficult. In this study, the effectiveness of joint linkage QTL analysis was evaluated on combinations of two to six nested RIL populations differing in inbreeding generation, phenotypic assay method, and/or marker set used in genotyping. In comparison to linkage analysis in a single population, identification of QTL by joint linkage analysis was only minimally affected by different phenotypic methods used among populations once phenotypic data were standardized. In contrast, genotyping of populations with only partially overlapping sets of markers had a marked negative effect on QTL detection by joint linkage analysis. In total, 16 genetic regions with QTL for partial resistance against P. sojae were identified, including four novel QTL on chromosomes 4, 9, 12, and 16, as well as significant genotype-by-isolate interactions. Resistance alleles from PI 427106 or PI 427105B contributed to a major QTL on chromosome 18, explaining 10-45% of the phenotypic variance. This case study provides guidance on the application of joint linkage QTL analysis of data collected from populations with heterogeneous assay conditions and a genetic framework for partial resistance to P. sojae.
机译:大豆对大豆疫霉的部分抗性受多重数量性状基因座(QTL)控制。使用传统的QTL映射方法,检测此类QTL(通常效果不大)的能力可能会受到总体规模的限制。巢式重组自交系(RIL)群体的联合连锁QTL分析通过增加群体规模,重组和等位基因多样性,提高了检测QTL的能力。但是,证明多个RIL种群的统一发育和表型鉴定很困难。在这项研究中,对两到六个嵌套的RIL群体的组合进行了评估,这些结合在近交世代,表型分析方法和/或基因分型中使用的标记集方面有所不同。与单个人群的连锁分析相比,一旦对表型数据进行标准化,通过联合连锁分析对QTL的识别仅受不同人群之间使用的不同表型方法的影响最小。相反,仅具有部分重叠标记集的人群的基因分型对通过联合连锁分析进行的QTL检测具有明显的负面影响。总共鉴定出16个具有QTL的部分抗大豆疫霉菌的QTL遗传区域,包括4、9、12和16号染色体上的四个新QTL,以及显着的基因型-分离株相互作用。来自PI 427106或PI 427105B的抗性等位基因促成了18号染色体上的主要QTL,解释了表型变异的10-45%。本案例研究为结合连锁QTL分析从具有不同检测条件和对大豆疫霉菌部分抗性的遗传框架的人群中收集的数据提供了指导。

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