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Epigenetic specification of centromeres.

机译:着丝粒的表观遗传学规范。

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Centromeres are the discrete sites of spindle microtubule attachment on chromosomes during mitosis and meiosis in all eukaryotes. These highly specialized chromatin structures typically occupy the same site for thousands of generations, yet the mechanism by which centromeres are established, maintained, and function remain a mystery. In metazoans, centromeric DNA sequence has proven not to be the key determinant of centromeric identity; therefore, centromeres are thought to be epigenetically specified by their specialized chromatin structure. In all eukaryotes, the centromere-specific histone H3 variant CenH3 replaces canonical H3 within nucleosomes at centric chromatin. This specialized nucleosome is the building block upon which all other centromere-associated proteins depend. This review highlights exciting new findings that have resulted in a paradigm shift in our understanding of CenH3 assembly into centromeric chromatin, CenH3 nucleosomal structure, CenH3 chromatin folding, the contribution of these factors to centromeric identity, and finally, the intimate role cell-cycle-regulated transcription and pericentric heterochromatin play in the maintenance and integrity of centromeres.
机译:着丝粒是所有真核生物在有丝分裂和减数分裂过程中染色体上纺锤体微管附着的离散位点。这些高度专业化的染色质结构通常占据数千个世代的相同位点,但建立,维持着丝粒的机制和作用仍然是个谜。在后生动物中,着丝粒DNA序列不是决定着丝粒身份的关键因素。因此,着丝粒被认为是由其专门的染色质结构在表观遗传上指定的。在所有真核生物中,着丝粒特异的组蛋白H3变体CenH3取代了中心染色质上核小体中的规范H3。这种专门的核小体是所有其他着丝粒相关蛋白所依赖的构建基。这篇综述突出了令人兴奋的新发现,这些发现导致我们对CenH3装配体的理解发生了转变,转变为着丝粒染色质,CenH3核小体结构,CenH3染色质折叠,这些因素对着丝粒身份的贡献,以及最后,细胞周期-亲密作用。调节转录和外周中心异染色质在着丝粒的维持和完整性中发挥作用。

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