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Mrc1 调控亲代组蛋白的分离和异染色质的遗传。

Mrc1 regulates parental histone segregation and heterochromatin inheritance.

机构信息

Department of Biological Sciences, Columbia University, New York, NY 10027, USA.

Department of Biological Sciences, Columbia University, New York, NY 10027, USA; State Key Laboratory of Plant Genomics, Institute of Microbiology, Chinese Academy of Sciences, Beijing 100101, China.

出版信息

Mol Cell. 2024 Sep 5;84(17):3223-3236.e4. doi: 10.1016/j.molcel.2024.07.002. Epub 2024 Aug 1.

Abstract

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.

摘要

基于染色质的表观遗传记忆依赖于亲本组蛋白在 DNA 复制机制内的组蛋白伴侣的辅助下,对称地分配到新合成的子代 DNA 链上。然而,亲本组蛋白转移的机制仍不清楚。在这里,我们揭示了在裂殖酵母中,复制体蛋白 Mrc1 在促进亲本组蛋白 H3-H4 转移到滞后链上起着至关重要的作用,确保了适当的异染色质遗传。此外,Mrc1 促进了 Mcm2 和 DNA 聚合酶 α 之间的相互作用,这两种蛋白对于亲本组蛋白转移至关重要。此外,Mrc1 参与亲本组蛋白转移和表观遗传遗传是独立于其在 DNA 复制检查点激活和复制体速度控制中的已知功能。相反,Mrc1 在其组蛋白结合区域之外与 Mcm2 相互作用,形成一个物理障碍,将亲本组蛋白转移途径分开。这些发现揭示了 Mrc1 作为复制体中的关键参与者,协调亲本组蛋白的分离以调节表观遗传遗传。

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