van den Berg Irene, Fritz Sébastien, Rodriguez Sabrina, Rocha Dominique, Boussaha Mekki, Lund Mogens S, Boichard Didier
INRA, UMR1313 Génétique Animale et Biologie Intégrative, 78350 Jouy-en-Josas, France.
Genet Sel Evol. 2014 May 19;46(1):31. doi: 10.1186/1297-9686-46-31.
The present availability of sequence data gives new opportunities to narrow down from QTL (quantitative trait locus) regions to causative mutations. Our objective was to decrease the number of candidate causative mutations in a QTL region. For this, a concordance analysis was applied for a leg conformation trait in dairy cattle. Several QTL were detected for which the QTL status (homozygous or heterozygous for the QTL) was inferred for each individual. Subsequently, the inferred QTL status was used in a concordance analysis to reduce the number of candidate mutations.
Twenty QTL for rear leg set side view were mapped using Bayes C. Marker effects estimated during QTL mapping were used to infer the QTL status for each individual. Subsequently, polymorphisms present in the QTL regions were extracted from the whole-genome sequences of 71 Holstein bulls. Only polymorphisms for which the status was concordant with the QTL status were kept as candidate causative mutations.
QTL status could be inferred for 15 of the 20 QTL. The number of concordant polymorphisms differed between QTL and depended on the number of QTL statuses that could be inferred and the linkage disequilibrium in the QTL region. For some QTL, the concordance analysis was efficient and narrowed down to a limited number of candidate mutations located in one or two genes, while for other QTL a large number of genes contained concordant polymorphisms.
For regions for which the concordance analysis could be performed, we were able to reduce the number of candidate mutations. For part of the QTL, the concordant analyses narrowed QTL regions down to a limited number of genes, of which some are known for their role in limb or skeletal development in humans and mice. Mutations in these genes are good candidates for QTN (quantitative trait nucleotides) influencing rear leg set side view.
目前序列数据的可得性为从数量性状基因座(QTL)区域缩小到致病突变提供了新机会。我们的目标是减少QTL区域中候选致病突变的数量。为此,对奶牛的腿部形态性状进行了一致性分析。检测到了几个QTL,并推断出每个个体的QTL状态(QTL的纯合或杂合)。随后,将推断出的QTL状态用于一致性分析,以减少候选突变的数量。
使用贝叶斯C方法定位了20个后肢侧视图的QTL。在QTL定位过程中估计的标记效应用于推断每个个体的QTL状态。随后,从71头荷斯坦公牛的全基因组序列中提取QTL区域中存在的多态性。只有状态与QTL状态一致的多态性才被保留为候选致病突变。
20个QTL中的15个可以推断出QTL状态。一致多态性的数量在不同QTL之间有所不同,并且取决于可以推断出的QTL状态的数量以及QTL区域中的连锁不平衡。对于一些QTL,一致性分析是有效的,并缩小到位于一个或两个基因中的有限数量的候选突变,而对于其他QTL,大量基因包含一致的多态性。
对于可以进行一致性分析的区域,我们能够减少候选突变的数量。对于部分QTL,一致性分析将QTL区域缩小到有限数量的基因,其中一些基因在人类和小鼠的肢体或骨骼发育中的作用是已知的。这些基因中的突变是影响后肢侧视图的数量性状核苷酸(QTN)的良好候选者。