Xu Jiale, Dai Xiongtao, Ramasamy Ramesh K, Wang Le, Zhu Tingting, McGuire Patrick E, Jorgensen Chad M, Dehghani Hamid, Gulick Patrick J, Luo Ming-Cheng, Müller Hans-Georg, Dvorak Jan
Department of Plant Sciences, University of California, Davis, California.
Department of Statistics, Iowa State University, Iowa.
G3 (Bethesda). 2019 Mar 7;9(3):841-853. doi: 10.1534/g3.118.200921.
Numerous quantitative trait loci (QTL) have been mapped in tetraploid and hexaploid wheat and wheat relatives, mostly with simple sequence repeat (SSR) or single nucleotide polymorphism (SNP) markers. To conduct meta-analysis of QTL requires projecting them onto a common genomic framework, either a consensus genetic map or genomic sequence. The latter strategy is pursued here. Of 774 QTL mapped in wheat and wheat relatives found in the literature, 585 (75.6%) were successfully projected onto the pseudomolecules. QTL mapped with SNP markers were more successfully projected (92.2%) than those mapped with SSR markers (66.2%). The QTL were not distributed homogeneously along chromosome arms. Their frequencies increased in the proximal-to-distal direction but declined in the most distal regions and were weakly correlated with recombination rates along the chromosome arms. Databases for projected SSR markers and QTL were constructed and incorporated into the JBrowse. To facilitate meta-QTL analysis, eight clusters of QTL were used to estimate standard deviations ([Formula: see text]) of independently mapped QTL projected onto the genome sequence. The standard deviations [Formula: see text] were modeled as an exponential decay function of recombination rates along the chromosomes. We implemented four hypothesis tests for determining the membership of query QTL. The hypothesis tests and estimation procedure for [Formula: see text] were implemented in a web portal for meta-analysis of projected QTL. Twenty-one QTL for head blight resistance mapped on wheat chromosomes 3A, 3B, and 3D were analyzed to illustrate the use of the portal for meta-QTL analyses.
许多数量性状位点(QTL)已在四倍体和六倍体小麦及其近缘种中定位,大多使用简单序列重复(SSR)或单核苷酸多态性(SNP)标记。进行QTL的荟萃分析需要将它们投影到一个共同的基因组框架上,即共识遗传图谱或基因组序列。本文采用后一种策略。在文献中发现的774个定位在小麦及其近缘种中的QTL中,有585个(75.6%)成功投影到了假分子上。用SNP标记定位的QTL比用SSR标记定位的QTL更成功地投影(92.2%对66.2%)。QTL并非沿染色体臂均匀分布。它们的频率从近端到远端方向增加,但在最远端区域下降,并且与沿染色体臂的重组率弱相关。构建了投影SSR标记和QTL的数据库,并将其整合到JBrowse中。为便于进行元QTL分析,使用了八个QTL簇来估计投影到基因组序列上的独立定位QTL的标准差([公式:见原文])。标准差[公式:见原文]被建模为沿染色体的重组率的指数衰减函数。我们实施了四个假设检验来确定查询QTL的归属。标准差[公式:见原文]的假设检验和估计程序在一个用于投影QTL荟萃分析的网络门户中实现。对定位在小麦3A、3B和3D染色体上的21个抗赤霉病QTL进行了分析,以说明该门户在元QTL分析中的应用。