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A haploid affair: core histone transitions during spermatogenesis.

机译:单倍体事件:在精子发生过程中核心组蛋白转变。

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The process of meiosis reduces a diploid cell to four haploid gametes and is accompanied by extensive recombination. Thus, the dynamics of chromatin during meiosis are significantly different than in mitotic cells. As spermatogenesis progresses, there is a widespread reorganization of the haploid genome followed by extensive DNA compaction. It has become increasingly clear that the dynamic composition of chromatin plays a critical role in the activities of enzymes and processes that act upon it. Therefore, an analysis of the role of histone variants and modifications in these processes may shed light upon the mechanisms involved and the control of chromatin structure in general. Histone variants such as histone H3.3, H2AX, and macroH2A appear to play key roles in the various stages of spermiogenesis, in addition to the specifically modulated acetylation of histone H4 (acH4), ubiquitination of histones H2A and H2B (uH2A, uH2B), and phosphorylation of histone H3 (H3p). This review will examine recent discoveries concerning the role of histone modifications and variants during meiosis and spermatogenesis.
机译:减数分裂过程将二倍体细胞减少为四个单倍体配子,并伴随着广泛的重组。因此,减数分裂过程中染色质的动力学与有丝分裂细胞中的显着不同。随着精子发生的进展,单倍体基因组发生了广泛的重组,随后发生了广泛的DNA紧缩。越来越清楚的是,染色质的动态组成在酶的活性和对其起作用的过程中起着至关重要的作用。因此,对组蛋白变体和修饰在这些过程中的作用进行分析,可能会揭示所涉及的机制和染色质结构的总体控制。组蛋白变体,例如组蛋白H3.3,H2AX和macroH2A,似乎在精子发生的各个阶段起着关键作用,除了组蛋白H4(acH4)的乙酰化被专门调节,组蛋白H2A和H2B(uH2A,uH2B)泛素化,以及组蛋白H3(H3p)的磷酸化。这项审查将审查有关组蛋白修饰和变体在减数分裂和生精过程中的作用的最新发现。

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