Lenormand Thomas
CEFE-Centre National de la Recherche Scientifique, 34293 Montpellier, France.
Genetics. 2003 Feb;163(2):811-22. doi: 10.1093/genetics/163.2.811.
Sex dimorphism in recombination is widespread on both sex chromosomes and autosomes. Various hypotheses have been proposed to explain these dimorphisms. Yet no theoretical model has been explored to determine how heterochiasmy--the autosomal dimorphism--could evolve. The model presented here shows three circumstances in which heterochiasmy is likely to evolve: (i) a male-female difference in haploid epistasis, (ii) a male-female difference in cis-epistasis minus trans-epistasis in diploids, or (iii) a difference in epistasis between combinations of genes inherited maternally or paternally. These results hold even if sources of linkage disequilibria besides epistasis, such as migration or Hill-Robertson interference, are considered and shed light on previous verbal models of sex dimorphism in recombination rates. Intriguingly, these results may also explain why imprinted regions on the autosomes of humans or sheep are particularly heterochiasmate.
重组中的性别二态性在性染色体和常染色体上普遍存在。人们提出了各种假说来解释这些二态性。然而,尚未探索出理论模型来确定常染色体二态性——异交叉现象是如何进化的。本文提出的模型显示了异交叉现象可能进化的三种情况:(i)单倍体上位性中的雌雄差异,(ii)二倍体中顺式上位性减去反式上位性的雌雄差异,或(iii)母系或父系遗传的基因组合之间上位性的差异。即使考虑到除上位性之外的连锁不平衡来源,如迁移或希尔-罗伯逊干扰,这些结果仍然成立,并为先前关于重组率性别二态性的文字模型提供了启示。有趣的是,这些结果也可能解释为什么人类或绵羊常染色体上的印记区域特别具有异交叉现象。