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人类内着丝粒 CCAN 复合物的结构及其对人类着丝粒组织的意义。

Structure of the human inner kinetochore CCAN complex and its significance for human centromere organization.

机构信息

Department of Mechanistic Cell Biology, Max-Planck Institute of Molecular Physiology, Otto-Hahn-Straße 11, 44227 Dortmund, Germany.

Department of Structural Biochemistry, Max-Planck Institute of Molecular Physiology, Otto-Hahn-Straße 11, 44227 Dortmund, Germany.

出版信息

Mol Cell. 2022 Jun 2;82(11):2113-2131.e8. doi: 10.1016/j.molcel.2022.04.027. Epub 2022 May 6.

Abstract

Centromeres are specialized chromosome loci that seed the kinetochore, a large protein complex that effects chromosome segregation. A 16-subunit complex, the constitutive centromere associated network (CCAN), connects between the specialized centromeric chromatin, marked by the histone H3 variant CENP-A, and the spindle-binding moiety of the kinetochore. Here, we report a cryo-electron microscopy structure of human CCAN. We highlight unique features such as the pseudo GTPase CENP-M and report how a crucial CENP-C motif binds the CENP-LN complex. The CCAN structure has implications for the mechanism of specific recognition of the CENP-A nucleosome. A model consistent with our structure depicts the CENP-C-bound nucleosome as connected to the CCAN through extended, flexible regions of CENP-C. An alternative model identifies both CENP-C and CENP-N as specificity determinants but requires CENP-N to bind CENP-A in a mode distinct from the classical nucleosome octamer.

摘要

着丝粒是一种特化的染色体位点,它为动粒(一种大型蛋白质复合物,能够促使染色体分离)提供种子。一个由 16 个亚基组成的复合物,即组成性着丝粒相关网络(CCAN),将由组蛋白 H3 变体 CENP-A 标记的特化着丝粒染色质与动粒的纺锤体结合部分连接起来。在这里,我们报告了人类 CCAN 的低温电子显微镜结构。我们强调了一些独特的特征,如假 GTPase CENP-M,并报告了关键的 CENP-C 基序如何结合 CENP-LN 复合物。CCAN 结构对 CENP-A 核小体特异性识别的机制有影响。与我们的结构一致的模型将 CENP-C 结合的核小体描绘为通过 CENP-C 的扩展、灵活区域与 CCAN 连接。另一种模型将 CENP-C 和 CENP-N 都确定为特异性决定因素,但需要 CENP-N 以不同于经典核小体八聚体的模式结合 CENP-A。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/02aa/9235857/1fb9f364d53e/fx1.jpg

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