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At the right place at the right time: novel CENP-A binding proteins shed light on centromere assembly

机译:在正确的时间,正确的位置:新颖的CENP-A结合蛋白阐明着丝粒的组装

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摘要

Centromeres, the chromosomal loci that form the sites of attachment for spindle microtubules during mitosis, are identified by a unique chromatin structure generated by nucleosomes containing the histone H3 variant CENP-A. The apparent epigenetic mode of centromere inheritance across mitotic and meiotic divisions has generated much interest in how CENP-A assembly occurs and how structurally divergent centromeric nucleosomes can specify the centromere complex. Although a substantial number of proteins have been implicated in centromere assembly, factors that can bind CENP-A specifically and deliver nascent protein to the centromere were, thus far, lacking. Several recent reports on experiments in fission yeast and human cells have now shown significant progress on this problem. Here, we discuss these new developments and their implications for epigenetic centromere inheritance. Communicated by E.A. Nigg
机译:着丝粒是在有丝分裂期间形成纺锤体微管附着位点的染色体位点,通过含有组蛋白H3变体CENP-A的核小体生成的独特染色质结构来鉴定。着丝粒和减数分裂分裂之间着丝粒遗传的明显表观遗传模式引起了人们对CENP-A组装如何发生以及结构上不同的着丝粒核小体如何确定着丝粒复合体的兴趣。尽管已经有大量蛋白质参与着丝粒的组装,但到目前为止,尚缺乏能够特异性结合CENP-A并将新生蛋白质传递到着丝粒的因子。关于裂变酵母和人类细胞的实验的最新报道现在显示出在该问题上的重大进展。在这里,我们讨论这些新的发展及其对表观遗传着丝粒遗传的影响。由E.A.沟通尼格

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