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组蛋白甲基化标记确保有丝分裂过程中染色体的完整性。

Bookmarking by histone methylation ensures chromosomal integrity during mitosis.

机构信息

Department of Pharmacology, School of Medicine, Kyung Hee University, Seoul, 02447, Republic of Korea.

出版信息

Arch Pharm Res. 2019 Jun;42(6):466-480. doi: 10.1007/s12272-019-01156-7. Epub 2019 Apr 24.

Abstract

The cell cycle is an orchestrated process that replicates DNA and transmits genetic information to daughter cells. Cell cycle progression is governed by diverse histone modifications that control gene transcription in a timely fashion. Histone modifications also regulate cell cycle progression by marking specific chromatic regions. While many reviews have covered histone phosphorylation and acetylation as regulators of the cell cycle, little attention has been paid to the roles of histone methylation in the faithful progression of mitosis. Indeed, specific histone methylations occurring before, during, or after mitosis affect kinetochore assembly and chromosome condensation and segregation. In addition to timing, histone methylations specify the chromatin regions such as chromosome arms, pericentromere, and centromere. Therefore, spatiotemporal programming of histone methylations ensures epigenetic inheritance through mitosis. This review mainly discusses histone methylations and their relevance to mitotic progression.

摘要

细胞周期是一个精心编排的过程,它复制 DNA 并将遗传信息传递给子细胞。细胞周期的进行受多种组蛋白修饰的控制,这些修饰以适时的方式控制基因转录。组蛋白修饰还通过标记特定的染色质区域来调节细胞周期的进行。虽然许多综述已经涵盖了组蛋白磷酸化和乙酰化作为细胞周期的调节剂,但组蛋白甲基化在有丝分裂中忠实进行的作用却很少受到关注。事实上,发生在有丝分裂之前、期间或之后的特定组蛋白甲基化会影响着动粒的组装以及染色体的浓缩和分离。除了定时之外,组蛋白甲基化还特异性地标记染色质区域,如染色体臂、着丝粒和着丝粒。因此,组蛋白甲基化的时空编程确保了通过有丝分裂进行的表观遗传遗传。这篇综述主要讨论了组蛋白甲基化及其与有丝分裂进程的相关性。

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