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How to build a centromere: from centromeric and pericentromeric chromatin to kinetochore assembly

机译:如何建立着丝粒:从着丝粒和着丝粒染色质到动粒组装

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The assembly of the centromere, a specialized region of DNA along with a constitutive protein complex which resides at the primary constriction and is the site of kinetochore formation, has been puzzling biologists for many years. Recent advances in the fields of chromatin, microscopy, and proteomics have shed a new light on this complex and essential process. Here we review recently discovered mechanisms and proteins involved in determining mammalian centromere location and assembly. The centromeric core protein CENP-A, a histone H3 variant, is hypothesized to designate centromere localization by incorporation into centromere-specific nucleosomes and is essential for the formation of a functional kinetochore. It has been found that centromere localization of centromere protein A (CENP-A), and therefore centromere determination, requires proteins involved in histone deacetylation, as well as base excision DNA repair pathways and proteolysis. In addition to the incorporation of CENP-A at the centromere, the formation of heterochromatin through histone methylation and RNA interference is also crucial for centromere formation. The assembly of the centromere and kinetochore is complex and interdependent, involving epigenetics and hierarchical protein–protein interactions.
机译:着丝粒的组装是DNA的一个特殊区域,它与构成蛋白质的复合物(位于主要颈缩处,是线粒体的形成位点)一起,多年来一直困扰着生物学家。染色质,显微镜和蛋白质组学领域的最新进展为这一复杂而必不可少的过程提供了新的思路。在这里,我们回顾最近发现的机制和蛋白质参与确定哺乳动物着丝粒的位置和组装。着丝粒核心蛋白CENP-A(一种组蛋白H3变体)被认为通过结合到着丝粒特异性核小体中来指定着丝粒定位,并且对功能性动粒的形成至关重要。已经发现,着丝粒蛋白A(CENP-A)的着丝粒定位以及因此着丝粒的确定需要蛋白质参与组蛋白去乙酰化以及碱基切除DNA修复途径和蛋白水解。除了在着丝粒处掺入CENP-A以外,通过组蛋白甲基化和RNA干扰形成异染色质对于着丝粒形成也至关重要。着丝粒和动粒体的组装是复杂且相互依存的,涉及表观遗传学和蛋白质间的相互作用。

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