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定量显微镜揭示着丝粒染色质稳定性、大小及维持着丝粒稳态的细胞周期机制。

Quantitative Microscopy Reveals Centromeric Chromatin Stability, Size, and Cell Cycle Mechanisms to Maintain Centromere Homeostasis.

作者信息

Stankovic Ana, Jansen Lars E T

机构信息

Instituto Gulbenkian de Ciência, 2780-156, Oeiras, Portugal.

出版信息

Prog Mol Subcell Biol. 2017;56:139-162. doi: 10.1007/978-3-319-58592-5_6.

Abstract

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.

摘要

着丝粒是由包含组蛋白H3变体CENP-A的核小体所指定的染色质结构域。这种独特的着丝粒结构是一种强大的自我模板化表观遗传机制的核心,该机制使着丝粒具有遗传性。我们综述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动粒的拷贝数、结构、大小和动力学。这些研究揭示,着丝粒长期维持的关键在于CENP-A核小体的缓慢周转、染色质结构域的临界大小及其与细胞周期偶联的复制。这些特征共同维持了一个染色质位点的稳态,该位点指导自身的表观遗传遗传并促进有丝分裂动粒的组装。

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