Morelli Meisha A, Cohen Paula E
Department of Biomedical Sciences, Cornell University, Ithaca, NY 14853, USA.
Reproduction. 2005 Dec;130(6):761-81. doi: 10.1530/rep.1.00865.
The study of mammalian meiosis is complicated by the timing of meiotic events in females and by the intermingling of meiotic sub-stages with somatic cells in the gonad of both sexes. In addition, studies of mouse mutants for different meiotic regulators have revealed significant differences in the stringency of meiotic events in males versus females. This sexual dimorphism implies that the processes of recombination and homologous chromosome pairing, while being controlled by similar genetic pathways, are subject to different levels of checkpoint control in males and females. This review is focused on the emerging picture of sexual dimorphism exhibited by mammalian germ cells using evidence from the broad range of meiotic mutants now available in the mouse. Many of these mouse mutants display distinct differences in meiotic progression and/or dysfunction in males versus females, and their continued study will allow us to understand the molecular basis for the sex-specific differences observed during prophase I progression.
哺乳动物减数分裂的研究因雌性减数分裂事件的时间安排以及两性性腺中减数分裂亚阶段与体细胞的混合而变得复杂。此外,对不同减数分裂调节因子的小鼠突变体的研究揭示了雄性和雌性减数分裂事件严格程度的显著差异。这种性别二态性意味着重组和同源染色体配对过程虽然由相似的遗传途径控制,但在雄性和雌性中受到不同水平的检查点控制。本综述聚焦于利用目前小鼠中广泛存在的减数分裂突变体的证据所呈现出的哺乳动物生殖细胞性别二态性的新情况。这些小鼠突变体中的许多在雄性和雌性的减数分裂进程和/或功能障碍方面表现出明显差异,对它们的持续研究将使我们能够理解在减数分裂前期进程中观察到的性别特异性差异的分子基础。