雄性生殖系有丝分裂和减数分裂细胞周期的调控。

D. Wolgemuth, Erika Laurion, Karen M. Lele
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引用次数: 90

摘要

哺乳动物配子发生为研究细胞周期调控提供了一个独特的系统。此外,了解控制生殖系有丝分裂和减数分裂的遗传程序将为理解不孕症和避孕提供新的方向。雄性和雌性生殖细胞具有共同的细胞周期调节阶段,包括有丝分裂增殖阶段、进入减数分裂阶段、完成还原性分裂阶段以及进入等待受精信号的静止状态。然而,这些事件发生的时间——实际上,甚至这些事件发生的发育阶段——在两性中是不同的。参与控制哺乳动物生殖细胞分化的这些特化有丝分裂和减数分裂周期的基因现在才被确定。它们包括一系列复杂的激酶、磷酸酶、调节蛋白(如细胞周期蛋白)和一系列同样复杂的底物,包括参与细胞分裂的核和细胞质结构的成分。本章概述了我们目前对哺乳动物有丝分裂细胞中细胞周期调控的理解以及限制点的重要性。摘要对小鼠配子中各种细胞周期调控基因的表达进行了观察,并对有丝分裂细胞和减数分裂细胞之间的有趣差异进行了评论。最后,对新型a型细胞周期蛋白cyclin A1在雄性减数分裂中的作用进行了深入讨论。
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Regulation of the mitotic and meiotic cell cycles in the male germ line.
Mammalian gametogenesis provides a unique system in which to study cell-cycle regulation. Furthermore, understanding the genetic program controlling the mitotic and meiotic divisions of the germ line will provide insight into understanding infertility and new directions for contraception. Male and female germ cells have stages of cell-cycle regulation in common, including a mitotic proliferative stage, entry into meiosis, completion of a reductive division, and entry into a quiescent state awaiting signals at fertilization. However, the timing of these events - and, indeed, even the stage of development at which these events occurs - differs in the two sexes. The genes involved in controlling these specialized mitotic and meiotic cycles of mammalian germ cell differentiation are only now being identified. They include a complex array of kinases, phosphatases, regulatory proteins (e.g., cyclins), and an equally complex array of substrates, including components of the nuclear and cytoplasmic structures involved in cell division. This chapter provides an overview of our current understanding of cell-cycle regulation in mammalian mitotic cells and the importance of restriction points. A summary of observations regarding the expression of various cell-cycle regulatory genes in mouse gametes is provided, along with comments on interesting differences between mitotic and meiotic cells. Finally, the role of the novel A-type cyclin, cyclin A1, during male meiosis is discussed in depth.
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