Department of Organismic and Evolutionary Biology, Harvard University, Cambridge, Massachusetts 02138
Department of Organismic and Evolutionary Biology, Harvard University, Cambridge, Massachusetts 02138.
Genetics. 2020 Dec;216(4):985-994. doi: 10.1534/genetics.120.303680. Epub 2020 Oct 27.
The genomic proportion that two relatives share identically by descent-their genetic relatedness-can vary depending on the history of recombination and segregation in their pedigree. Previous calculations of the variance of genetic relatedness have defined genetic relatedness as the proportion of total genetic map length (cM) shared by relatives, and have neglected crossover interference and sex differences in recombination. Here, we consider genetic relatedness as the proportion of the total physical genome (bp) shared by relatives, and calculate its variance for general pedigree relationships, making no assumptions about the recombination process. For the relationships of grandparent-grandoffspring and siblings, the variance of genetic relatedness is a simple decreasing function of [Formula: see text], the average proportion of locus pairs that recombine in meiosis. For general pedigree relationships, the variance of genetic relatedness is a function of metrics analogous to [Formula: see text] Therefore, features of the aggregate recombination process that affect [Formula: see text] and analogs also affect variance in genetic relatedness. Such features include the number of chromosomes and heterogeneity in their size, the number of crossovers and their spatial organization along chromosomes, and sex differences in recombination. Our calculations help to explain several recent observations about variance in genetic relatedness, including that it is reduced by crossover interference (which is known to increase [Formula: see text]). Our methods further allow us to calculate the neutral variance of ancestry among Fs in a hybrid cross, enabling precise statistical inference in F-based tests for various kinds of selection.
两个亲属通过同源遗传共享的基因组比例——他们的遗传相关性——可能因他们系谱中的重组和分离历史而异。先前计算遗传相关性的方差时,将遗传相关性定义为亲属共享的总遗传图谱长度 (cM) 的比例,并忽略了交叉干扰和重组中的性别差异。在这里,我们将遗传相关性视为亲属共享的总物理基因组 (bp) 的比例,并针对一般的系谱关系计算其方差,不假设重组过程。对于祖孙和兄弟姐妹的关系,遗传相关性的方差是[公式:见文本],即减数分裂中重组的基因座对的平均比例的简单递减函数。对于一般的系谱关系,遗传相关性的方差是类似于[公式:见文本]的度量的函数。因此,影响[公式:见文本]和类似物的总重组过程的特征也会影响遗传相关性的方差。这些特征包括染色体的数量及其大小的异质性、交叉的数量及其在染色体上的空间组织,以及重组中的性别差异。我们的计算有助于解释最近关于遗传相关性方差的几个观察结果,包括交叉干扰会降低遗传相关性(这已被证明会增加[公式:见文本])。我们的方法还使我们能够计算杂种杂交中 Fs 之间的中性祖先方差,从而能够在基于 F 的各种选择测试中进行精确的统计推断。