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基因的上位相互作用影响小鼠身体活动性状的个体内变异。

Epistatic interactions of genes influence within-individual variation of physical activity traits in mice.

作者信息

Leamy Larry J, Pomp Daniel, Lightfoot J Timothy

机构信息

Department of Biology, University of North Carolina, Charlotte, NC 28223, USA.

出版信息

Genetica. 2011 Jun;139(6):813-21. doi: 10.1007/s10709-011-9586-9. Epub 2011 Jun 11.

Abstract

A number of quantitative trait loci (QTLs) recently have been discovered that affect various activity traits in mice, but their collective impact does not appear to explain the consistently moderate to high heritabilities for these traits. We previously suggested interactions of genes, or epistasis, might account for additional genetic variability of activity, and tested this for the average distance, duration and speed run by mice during a 3 week period. We found abundant evidence for epistasis affecting these traits, although, recognized that epistatic effects may well vary within individuals over time. We therefore conducted a full genome scan for epistatic interactions affecting these traits in each of seven three-day intervals. Our intent was to assess the extent and trends in epistasis affecting these traits in each of the intervals. We discovered a number of epistatic interactions of QTLs that influenced the activity traits in the mice, the majority of which were not previously found and appeared to affect the activity traits (especially distance and speed) primarily in the early or in the late age intervals. The overall impact of epistasis was considerable, its contribution to the total phenotypic variance varying from an average of 22-35% in the three traits across all age intervals. It was concluded that epistasis is more important than single-locus effects of genes on activity traits at specific ages and it is therefore an essential component of the genetic architecture of physical activity.

摘要

最近发现了一些影响小鼠各种活动性状的数量性状基因座(QTL),但它们的综合影响似乎并不能解释这些性状一直保持的中等至高遗传力。我们之前曾提出基因间的相互作用,即上位性,可能是活动额外遗传变异性的原因,并针对小鼠在3周时间内的平均跑动距离、持续时间和速度进行了测试。我们发现了大量影响这些性状的上位性证据,不过也认识到上位性效应可能会随个体时间变化而有所不同。因此,我们在七个为期三天的时间段内,对影响这些性状的上位性相互作用进行了全基因组扫描。我们的目的是评估每个时间段内影响这些性状的上位性程度和趋势。我们发现了一些影响小鼠活动性状的QTL上位性相互作用,其中大多数是之前未发现的,并且似乎主要在早期或晚期年龄段影响活动性状(尤其是距离和速度)。上位性的总体影响相当可观,其对所有年龄段三个性状总表型方差的贡献平均在22%至35%之间。得出的结论是,在特定年龄,上位性比基因的单基因座效应在活动性状上更为重要,因此它是身体活动遗传结构的一个重要组成部分。

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