定量显微镜揭示着丝粒染色质的稳定性、大小和维持着丝粒稳态的细胞周期机制。

Q2 Medicine
Ana Stankovic, Lars E T Jansen
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引用次数: 6

摘要

着丝粒是由含有组蛋白H3变体CENP-A的核小体指定的染色质结构域。这种独特的着丝粒结构是强大的自我模板表观遗传机制的核心,使着丝粒具有遗传性。我们回顾了特定的定量显微镜方法如何有助于确定着丝粒染色质及其相关的着丝粒复合体和着丝点的拷贝数、结构、大小和动力学。这些努力揭示了着丝粒长期维持的关键是CENP-A核小体的缓慢周转,这是染色质结构域的临界大小及其细胞周期偶联复制。这些特征共同维持染色质位点的内稳态,从而指导其自身的表观遗传并促进有丝分裂着丝点的组装。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Quantitative Microscopy Reveals Centromeric Chromatin Stability, Size, and Cell Cycle Mechanisms to Maintain Centromere Homeostasis.

Centromeres are chromatin domains specified by nucleosomes containing the histone H3 variant, CENP-A. This unique centromeric structure is at the heart of a strong self-templating epigenetic mechanism that renders centromeres heritable. We review how specific quantitative microscopy approaches have contributed to the determination of the copy number, architecture, size, and dynamics of centromeric chromatin and its associated centromere complex and kinetochore. These efforts revealed that the key to long-term centromere maintenance is the slow turnover of CENP-A nucleosomes, a critical size of the chromatin domain and its cell cycle-coupled replication. These features come together to maintain homeostasis of a chromatin locus that directs its own epigenetic inheritance and facilitates the assembly of the mitotic kinetochore.

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来源期刊
CiteScore
3.30
自引率
0.00%
发文量
7
期刊介绍: Molecular biology has been providing an overwhelming amount of data on the structural components and molecular machineries of the cell and its organelles and the complexity of intra- and intercellular communication. The molecular basis of hereditary and acquired diseases is beginning to be unravelled, and profound new insights into development and evolutionary biology have been gained from molecular approaches. Progress in Molecular and Subcellular Biology summarises the most recent developments in this fascinating area of biology.
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