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酵母 Ctf3 复合物的结构。

The structure of the yeast Ctf3 complex.

机构信息

Department of Biological Chemistry and Molecular Pharmacology, Harvard Medical School, Howard Hughes Medical Institute, Boston, United States.

Harvard Chemical Biology PhD Program, Harvard University, Boston, United States.

出版信息

Elife. 2019 Jun 13;8:e48215. doi: 10.7554/eLife.48215.

Abstract

Kinetochores are the chromosomal attachment points for spindle microtubules. They are also signaling hubs that control major cell cycle transitions and coordinate chromosome folding. Most well-studied eukaryotes rely on a conserved set of factors, which are divided among two loosely-defined groups, for these functions. Outer kinetochore proteins contact microtubules or regulate this contact directly. Inner kinetochore proteins designate the kinetochore assembly site by recognizing a specialized nucleosome containing the H3 variant Cse4/CENP-A. We previously determined the structure, resolved by cryo-electron microscopy (cryo-EM), of the yeast Ctf19 complex (Ctf19c, homologous to the vertebrate CCAN), providing a high-resolution view of inner kinetochore architecture (Hinshaw and Harrison, 2019). We now extend these observations by reporting a near-atomic model of the Ctf3 complex, the outermost Ctf19c sub-assembly seen in our original cryo-EM density. The model is sufficiently well-determined by the new data to enable molecular interpretation of Ctf3 recruitment and function.

摘要

着丝粒是纺锤体微管的染色体附着点。它们也是信号枢纽,控制着主要的细胞周期转变,并协调染色体折叠。大多数研究充分的真核生物依赖于一组保守的因子来实现这些功能,这些因子分为两个定义不严格的组。外着丝粒蛋白与微管接触或直接调节这种接触。内着丝粒蛋白通过识别含有 H3 变体 Cse4/CENP-A 的特殊核小体来指定着丝粒组装位点。我们之前通过低温电子显微镜(cryo-EM)解析了酵母 Ctf19 复合物(Ctf19c,与脊椎动物的 CCAN 同源)的结构,提供了内着丝粒结构的高分辨率视图(Hinshaw 和 Harrison,2019)。我们现在通过报告 Ctf3 复合物的近原子模型来扩展这些观察结果,该模型是我们原始 cryo-EM 密度中观察到的最外层 Ctf19c 亚基。该模型由新数据充分确定,能够对 Ctf3 的募集和功能进行分子解释。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6244/6602579/6b698ab82bff/elife-48215-fig1.jpg

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