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酵母中 DNA 复制过程中组蛋白的双亲性回收模式和参与者。

The patterns and participants of parental histone recycling during DNA replication in Saccharomyces cerevisiae.

机构信息

National Laboratory of Biomacromolecules, CAS Center for Excellence in Biomacromolecules, Institute of Biophysics, Chinese Academy of Sciences, Beijing, 100101, China.

College of Life Sciences, University of Chinese Academy of Sciences, Beijing, 100049, China.

出版信息

Sci China Life Sci. 2023 Jul;66(7):1600-1614. doi: 10.1007/s11427-022-2267-6. Epub 2023 Mar 9.

Abstract

Epigenetic information carried by histone modifications not only reflects the state of gene expression, but also participates in the maintenance of chromatin states and the regulation of gene expression. Recycling of parental histones to daughter chromatin after DNA replication is vital to mitotic inheritance of epigenetic information and the maintenance of cell identity, because the locus-specific modifications of the parental histones need to be maintained. To assess the precision of parental histone recycling, we developed a synthetic local label-chasing system in budding yeast Saccharomyces cerevisiae. Using this system, we observed that parental histone H3 can be recycled to their original position, thereby recovering their position information after DNA replication at all tested loci, including heterochromatin boundary, non-transcribed region, and actively transcribed regions. Moreover, the recycling rate appears to be affected by local chromatin environment. We surveyed a number of potential regulatory factors and observed that histone H3-H4 chaperon Asf1 contributed to parental histone recycling, while the eukaryotic replisome-associated components Mcm2 and Dpb3 displayed compounding effects in this process. In addition, the FACT complex also plays a role in the recycling of parental histones and helps to stabilize the nucleosomes.

摘要

组蛋白修饰所携带的表观遗传信息不仅反映了基因表达的状态,还参与了染色质状态的维持和基因表达的调控。在有丝分裂过程中,亲代组蛋白向子染色质的回收对于表观遗传信息的有丝分裂遗传和细胞身份的维持至关重要,因为需要维持亲代组蛋白的局部位点修饰。为了评估亲代组蛋白回收的精确性,我们在 budding yeast Saccharomyces cerevisiae 中开发了一种合成的局部标记追踪系统。使用该系统,我们观察到亲代组蛋白 H3 可以被回收至其原始位置,从而在所有测试的位点(包括异染色质边界、非转录区和活跃转录区)恢复其 DNA 复制后的位置信息。此外,回收速率似乎受到局部染色质环境的影响。我们调查了一些潜在的调控因子,并观察到组蛋白 H3-H4 伴侣蛋白 Asf1 有助于亲代组蛋白的回收,而真核复制体相关成分 Mcm2 和 Dpb3 在这个过程中显示出叠加效应。此外,FACT 复合物也在亲代组蛋白的回收中发挥作用,并有助于稳定核小体。

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