Mrc1调控亲本组蛋白分离和异染色质遗传

IF 14.5 1区 生物学 Q1 BIOCHEMISTRY & MOLECULAR BIOLOGY
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引用次数: 0

摘要

基于染色质的表观遗传记忆依赖于亲代组蛋白在 DNA 复制机制中组蛋白伴侣的帮助下对称地分布到新合成的子代 DNA 链上。然而,亲代组蛋白转移的机制仍然难以捉摸。在这里,我们揭示了在裂殖酵母中,复制体蛋白Mrc1在促进亲代组蛋白H3-H4向滞后链转移方面发挥着关键作用,从而确保了异染色质的正常遗传。此外,Mrc1 还能促进 Mcm2 和 DNA 聚合酶α(这两种组蛋白结合蛋白对亲代组蛋白转移至关重要)之间的相互作用。此外,Mrc1参与亲代组蛋白转移和表观遗传与它在DNA复制检查点激活和复制体速度控制方面的已知功能无关。相反,Mrc1在其组蛋白结合区之外与Mcm2相互作用,为分离亲代组蛋白转移途径创造了物理屏障。这些发现揭示了Mrc1在复制体中的关键作用,它协调亲本组蛋白分离,调节表观遗传。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Mrc1 regulates parental histone segregation and heterochromatin inheritance

Mrc1 regulates parental histone segregation and heterochromatin inheritance

Chromatin-based epigenetic memory relies on the symmetric distribution of parental histones to newly synthesized daughter DNA strands, aided by histone chaperones within the DNA replication machinery. However, the mechanism of parental histone transfer remains elusive. Here, we reveal that in fission yeast, the replisome protein Mrc1 plays a crucial role in promoting the transfer of parental histone H3-H4 to the lagging strand, ensuring proper heterochromatin inheritance. In addition, Mrc1 facilitates the interaction between Mcm2 and DNA polymerase alpha, two histone-binding proteins critical for parental histone transfer. Furthermore, Mrc1’s involvement in parental histone transfer and epigenetic inheritance is independent of its known functions in DNA replication checkpoint activation and replisome speed control. Instead, Mrc1 interacts with Mcm2 outside of its histone-binding region, creating a physical barrier to separate parental histone transfer pathways. These findings unveil Mrc1 as a key player within the replisome, coordinating parental histone segregation to regulate epigenetic inheritance.

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来源期刊
Molecular Cell
Molecular Cell 生物-生化与分子生物学
CiteScore
26.00
自引率
3.80%
发文量
389
审稿时长
1 months
期刊介绍: Molecular Cell is a companion to Cell, the leading journal of biology and the highest-impact journal in the world. Launched in December 1997 and published monthly. Molecular Cell is dedicated to publishing cutting-edge research in molecular biology, focusing on fundamental cellular processes. The journal encompasses a wide range of topics, including DNA replication, recombination, and repair; Chromatin biology and genome organization; Transcription; RNA processing and decay; Non-coding RNA function; Translation; Protein folding, modification, and quality control; Signal transduction pathways; Cell cycle and checkpoints; Cell death; Autophagy; Metabolism.
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