Department of Biology and Biochemistry, University of Bath, Bath, BA2 7AY, United Kingdom.
Genetics. 2012 May;191(1):261-77. doi: 10.1534/genetics.111.136440. Epub 2012 Feb 29.
Great progress has been made in understanding the genetic architecture of phenotypic variation, but it is almost entirely focused on how the genotype of an individual affects the phenotype of that same individual. However, in many species the genotype of the mother is a major determinant of the phenotype of her offspring. Therefore, a complete picture of genetic architecture must include these maternal genetic effects, but they can be difficult to identify because maternal and offspring genotypes are correlated and therefore, partially confounded. We present a conceptual framework that overcomes this challenge to separate direct and maternal effects in intact families through an analysis that we call "statistical cross-fostering." Our approach combines genotype data from mothers and their offspring to remove the confounding effects of the offspring's own genotype on measures of maternal genetic effects. We formalize our approach in an orthogonal model and apply this model to an experimental population of mice. We identify a set of six maternal genetic effect loci that explain a substantial portion of variation in body size at all ages. This variation would be missed in an approach focused solely on direct genetic effects, but is clearly a major component of genetic architecture. Our approach can easily be adapted to examine maternal effects in different systems, and because it does not require experimental manipulation, it provides a framework that can be used to understand the contribution of maternal genetic effects in both natural and experimental populations.
在理解表型变异的遗传结构方面已经取得了很大的进展,但几乎完全集中在个体的基因型如何影响同一个体的表型。然而,在许多物种中,母亲的基因型是决定其后代表型的主要因素。因此,遗传结构的完整图景必须包括这些母系遗传效应,但由于母系和后代的基因型是相关的,因此部分是混淆的,所以它们很难识别。我们提出了一个概念框架,通过我们称之为“统计交叉寄养”的分析来克服这一挑战,从而在完整的家庭中分离直接效应和母系效应。我们的方法结合了来自母亲及其后代的基因型数据,以消除后代自身基因型对母系遗传效应度量的混杂影响。我们在正交模型中形式化了我们的方法,并将该模型应用于一个实验小鼠群体。我们确定了一组六个母系遗传效应位点,这些位点解释了在所有年龄段的体型上的大部分变异。如果只关注直接遗传效应,这种变异就会被忽略,但它显然是遗传结构的一个主要组成部分。我们的方法可以很容易地适应于研究不同系统中的母系效应,而且由于它不需要实验操作,因此提供了一个可以用于理解自然和实验种群中母系遗传效应贡献的框架。