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小鼠下颌骨大小波动不对称的上位遗传基础。

An epistatic genetic basis for fluctuating asymmetry of mandible size in mice.

作者信息

Leamy Larry J, Routman Eric J, Cheverud James M

机构信息

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

出版信息

Evolution. 2002 Mar;56(3):642-53. doi: 10.1111/j.0014-3820.2002.tb01373.x.

Abstract

The genetic basis of fluctuating asymmetry (FA), or nondirectional variation in the subtle differences between left and right sides of bilateral characters, continues to be of considerable theoretical interest. FA generally has been thought to arise from random noise during development and therefore to have a largely or entirely environmental origin. Whereas additive genetic variation for FA generally has been small and often insignificant, a number of investigators have hypothesized that interactions between loci, or epistasis, significantly influence FA. We tested this hypothesis by conducting a whole-genome scan to detect any epistasis in FA of centroid size in the mandibles of more than 400 mice from an F2 intercross population formed from crossing the Large (LG/J) and Small (SM/J) inbred strains. Genotypic deviations were imputed at each site 2 cM apart on all 19 autosomes, and these and centroid size asymmetry values were used in canonical correlation analyses for each of the 171 possible pairs of 19 autosomes to identify the most probable sites for epistasis. Epistasis for centroid size asymmetry was abundant, occurring far more often than was expected by chance alone (there were 30 separate instances of epistasis at the 0.001 significance level, when only two were expected by chance alone). The contributions of epistasis from 30 pairwise combinations of loci tended to suppress the additive and dominance genetic variance, but greatly increased the epistatic genetic variance for FA in centroid size given the intermediate allele frequencies of an F2 intercross population.

摘要

波动不对称性(FA),即双侧性状左右两侧细微差异中的非定向变异,其遗传基础一直备受理论关注。一般认为FA源于发育过程中的随机噪声,因此在很大程度上或完全由环境因素导致。虽然FA的加性遗传变异通常较小且往往不显著,但一些研究人员推测基因座之间的相互作用,即上位性,会对FA产生显著影响。我们通过全基因组扫描来检验这一假设,以检测由大(LG/J)和小(SM/J)近交系杂交形成的F2杂交群体中400多只小鼠下颌骨质心大小FA中的任何上位性。在所有19条常染色体上,每隔2厘摩的位点进行基因型偏差估算,并将这些数据和质心大小不对称值用于19条常染色体的171对可能组合中的每一对的典型相关分析,以确定最可能存在上位性的位点。质心大小不对称的上位性很丰富,其出现频率远远高于仅由随机因素预期的频率(在0.001显著水平下有30个独立的上位性实例,而仅由随机因素预期只有两个)。鉴于F2杂交群体的中间等位基因频率,30个基因座对组合的上位性贡献倾向于抑制加性和显性遗传方差,但大大增加了质心大小FA的上位性遗传方差。

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