Medical Research Council (MRC) Human Genetics Unit, MRC Institute of Genetics and Cancer, University of Edinburgh, Edinburgh, United Kingdom; email:
Wellcome Centre for Cell Biology, Institute of Cell Biology, University of Edinburgh, Edinburgh, United Kingdom; email:
Annu Rev Genomics Hum Genet. 2023 Aug 25;24:35-61. doi: 10.1146/annurev-genom-110122-090239. Epub 2023 May 9.
In meiosis, homologous chromosome synapsis is mediated by a supramolecular protein structure, the synaptonemal complex (SC), that assembles between homologous chromosome axes. The mammalian SC comprises at least eight largely coiled-coil proteins that interact and self-assemble to generate a long, zipper-like structure that holds homologous chromosomes in close proximity and promotes the formation of genetic crossovers and accurate meiotic chromosome segregation. In recent years, numerous mutations in human SC genes have been associated with different types of male and female infertility. Here, we integrate structural information on the human SC with mouse and human genetics to describe the molecular mechanisms by which SC mutations can result in human infertility. We outline certain themes in which different SC proteins are susceptible to different types of disease mutation and how genetic variants with seemingly minor effects on SC proteins may act as dominant-negative mutations in which the heterozygous state is pathogenic.
在减数分裂中,同源染色体的联会是由一个超分子蛋白质结构介导的,这个结构被称为联会复合体(SC),它在同源染色体轴之间组装。哺乳动物的 SC 至少由八个主要的卷曲螺旋蛋白组成,这些蛋白相互作用并自我组装,形成一个长的、拉链状的结构,将同源染色体紧密地保持在一起,并促进遗传交叉和准确的减数分裂染色体分离。近年来,人类 SC 基因的许多突变与不同类型的男性和女性不育症有关。在这里,我们将人类 SC 的结构信息与小鼠和人类遗传学相结合,描述 SC 突变如何导致人类不育的分子机制。我们概述了不同 SC 蛋白易受不同类型疾病突变的某些主题,以及对 SC 蛋白影响似乎较小的遗传变异如何作为显性负突变,其中杂合状态是致病的。