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在具有渐渗矮化基因的高粱关联群体中对株高数量性状位点进行高效定位。

Efficient mapping of plant height quantitative trait loci in a sorghum association population with introgressed dwarfing genes.

作者信息

Brown Patrick J, Rooney William L, Franks Cleve, Kresovich Stephen

机构信息

Institute for Genomic Diversity, Cornell University, Ithaca, New York 14853, USA.

出版信息

Genetics. 2008 Sep;180(1):629-37. doi: 10.1534/genetics.108.092239. Epub 2008 Aug 30.

Abstract

Of the four major dwarfing genes described in sorghum, only Dw3 has been cloned. We used association mapping to characterize the phenotypic effects of the dw3 mutation and to fine map a second, epistatic dwarfing QTL on sorghum chromosome 9 (Sb-HT9.1). Our panel of 378 sorghum inbreds includes 230 sorghum conversion (SC) lines, which are exotic lines that have been introgressed with dwarfing quantitative trait loci (QTL) from a common parent. The causal mutation in dw3 associates with reduced lower internode length and an elongation of the apex, consistent with its role as an auxin efflux carrier. Lines carrying the dw3 mutation display high haplotype homozygosity over several megabases in the Dw3 region, but most markers linked to Dw3 do not associate significantly with plant height due to allele sharing between Dw3 and dw3 individuals. Using markers with a high mutation rate and the dw3 mutation as an interaction term, significant trait associations were detected across a 7-Mb region around Sb-HT9.1, largely due to higher detection power in the SC lines. Conversely, the likely QTL interval for Sb-HT9.1 was reduced to approximately 100 kb, demonstrating that the unique structure of this association panel provides both power and resolution for a genomewide scan.

摘要

在高粱中描述的四个主要矮化基因中,只有Dw3已被克隆。我们利用关联作图来表征dw3突变的表型效应,并对高粱第9号染色体(Sb-HT9.1)上的第二个上位性矮化数量性状位点(QTL)进行精细定位。我们的378个高粱自交系群体包括230个高粱转换(SC)系,这些是从一个共同亲本导入了矮化数量性状位点(QTL)的外来系。dw3中的因果突变与下部节间长度缩短和顶端伸长有关,与其作为生长素输出载体的作用一致。携带dw3突变的品系在Dw3区域的几个兆碱基上表现出高单倍型纯合性,但由于Dw3和dw3个体之间的等位基因共享,大多数与Dw3连锁的标记与株高没有显著关联。使用具有高突变率的标记和dw3突变作为交互项,在Sb-HT9.1周围7兆碱基的区域检测到显著的性状关联,这主要是由于SC系中检测能力更高。相反,Sb-HT9.1可能的QTL区间缩小到约100 kb,表明该关联群体的独特结构为全基因组扫描提供了能力和分辨率。

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