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着丝粒组装和功能的表观基因组学。

Epigenomics of centromere assembly and function.

机构信息

Duke Institute for Genome Sciences & Policy and Department of Molecular Genetics and Microbiology, Duke University, 101 Science Drive, Box 3382, Durham, NC 27708, USA.

出版信息

Curr Opin Cell Biol. 2010 Dec;22(6):772-80. doi: 10.1016/j.ceb.2010.07.002. Epub 2010 Jul 31.

Abstract

The centromere is a complex chromosomal locus where the kinetochore is formed and microtubules attach during cell division. Centromere identity involves both genomic and sequence-independent (epigenetic) mechanisms. Current models for how centromeres are formed and, conversely, turned off have emerged from studies of unusual or engineered chromosomes, such as neocentromeres, artificial chromosomes, and dicentric chromosomes. Recent studies have highlighted the importance of unique chromatin marked by the histone H3 variant CENP-A, classical chromatin (heterochromatin and euchromatin), and transcription during centromere activation and inactivation. These advances have deepened our view of what defines a centromere and how it behaves in various genomic and chromatin contexts.

摘要

着丝粒是一个复杂的染色体位点,在细胞分裂过程中,动粒在这里形成,微管与之结合。着丝粒的身份既涉及基因组机制,也涉及序列非依赖性(表观遗传)机制。目前关于着丝粒如何形成以及相反地如何关闭的模型,是通过对异常或工程染色体(如新着丝粒、人工染色体和双着丝粒染色体)的研究而出现的。最近的研究强调了由组蛋白 H3 变体 CENP-A、经典染色质(异染色质和常染色质)和转录标记的独特染色质在着丝粒激活和失活过程中的重要性。这些进展加深了我们对定义着丝粒的认识,以及它在各种基因组和染色质环境中的行为。

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