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逐步展开支持脊椎动物动粒的亚基模型。

Stepwise unfolding supports a subunit model for vertebrate kinetochores.

作者信息

Vargiu Giulia, Makarov Alexandr A, Allan James, Fukagawa Tatsuo, Booth Daniel G, Earnshaw William C

机构信息

Wellcome Trust Centre for Cell Biology, University of Edinburgh, Edinburgh EH9 3BF, Scotland, United Kingdom.

MRC Human Genetics Unit, Institute of Genetics and Molecular Medicine, The University of Edinburgh, Edinburgh EH4 2XU, Scotland, United Kingdom.

出版信息

Proc Natl Acad Sci U S A. 2017 Mar 21;114(12):3133-3138. doi: 10.1073/pnas.1614145114. Epub 2017 Mar 6.

Abstract

During cell division, interactions between microtubules and chromosomes are mediated by the kinetochore, a proteinaceous structure located at the primary constriction of chromosomes. In addition to the centromere histone centromere protein A (CENP-A), 15 other members of the constitutive centromere associated network (CCAN) participate in the formation of a chromatin-associated scaffold that supports kinetochore structure. We performed a targeted screen analyzing unfolded centrochromatin from CENP-depleted chromosomes. Our results revealed that CENP-C and CENP-S are critical for the stable folding of mitotic kinetochore chromatin. Multipeak fitting algorithms revealed the presence of an organized pattern of centrochromatin packing consistent with arrangement of CENP-A-containing nucleosomes into up to five chromatin "subunits"-each containing roughly 20-30 nucleosomes. These subunits could be either layers of a boustrophedon or small loops of centromeric chromatin.

摘要

在细胞分裂过程中,微管与染色体之间的相互作用由动粒介导,动粒是位于染色体主缢痕处的一种蛋白质结构。除着丝粒组蛋白着丝粒蛋白A(CENP-A)外,组成型着丝粒相关网络(CCAN)的其他15个成员参与形成支持动粒结构的染色质相关支架。我们进行了一项靶向筛选,分析来自CENP缺失染色体的未折叠着丝粒染色质。我们的结果表明,CENP-C和CENP-S对有丝分裂动粒染色质的稳定折叠至关重要。多峰拟合算法揭示了着丝粒染色质堆积的有组织模式,这与含CENP-A的核小体排列成多达五个染色质“亚基”一致——每个亚基大致包含20-30个核小体。这些亚基可以是反向双股排列的层,也可以是着丝粒染色质的小环。

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