CCAN forms the spherical shell-like structure in interphase kinetochores

IF 13.9 1区 综合性期刊 Q1 MULTIDISCIPLINARY SCIENCES
Yuji Sakai, Mariko Ariyoshi, Yasuhiro Hirano, Yutaka Mahana, Aussie Suzuki, Toru Hirota, Masashi Tachikawa, Tatsuo Fukagawa
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引用次数: 0

Abstract

The kinetochore is an essential structure for the faithful chromosome segregation during mitosis. The 16-protein complex known as the constitutive centromere-associated network (CCAN) localizes the centromere throughout the cell cycle and forms the basis of the kinetochore. Although cryo–electron microscopy has provided a structural model of an individual CCAN unit, how multiple CCAN units are organized within cells remains unclear. Here, using in silico and in vivo analyses, we demonstrate that multiple CCAN units form a spherical shell-like structure in interphase DT40 kinetochores. CENP-T and CENP-N localize to the CCAN shell, whereas the CENP-C cupin domain clusters at the center. Molecular dynamics simulations of CCAN assembly suggest that CENP-C–DNA interactions constrain the orientation of CCAN units, supporting a spherical shell-like organization via CENP-C oligomerization. Super-resolution imaging reveals the spherical shell-like structure at DT40 kinetochores, and CENP-C knockout or expression of a CENP-C DNA binding deficient mutant abolishes the structure, consistent with the simulation-derived model. These findings provide important insights into the spatial organization of functional kinetochores within cells.
CCAN在间期着丝点形成球形壳状结构
着丝点是有丝分裂过程中染色体忠实分离的重要结构。在整个细胞周期中,由16个蛋白组成的着丝粒相关网络(CCAN)定位着丝粒,并构成着丝粒的基础。尽管低温电子显微镜已经提供了单个CCAN单元的结构模型,但细胞内多个CCAN单元是如何组织的仍不清楚。在这里,使用硅和体内分析,我们证明了多个CCAN单元在DT40间期着丝点中形成球形壳状结构。CENP-T和CENP-N定位于CCAN外壳,而CENP-C则位于中心。CCAN组装的分子动力学模拟表明,CENP-C - dna相互作用约束了CCAN单元的取向,通过CENP-C寡聚化支持球形壳状组织。超分辨率成像显示DT40的着丝点具有球形壳状结构,而敲除CENP-C或表达CENP-C DNA结合缺陷突变体会消除这种结构,这与模拟导出的模型一致。这些发现对细胞内功能性着丝点的空间组织提供了重要的见解。
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来源期刊
Science Advances
Science Advances 综合性期刊-综合性期刊
CiteScore
21.40
自引率
1.50%
发文量
1937
审稿时长
29 weeks
期刊介绍: Science Advances, an open-access journal by AAAS, publishes impactful research in diverse scientific areas. It aims for fair, fast, and expert peer review, providing freely accessible research to readers. Led by distinguished scientists, the journal supports AAAS's mission by extending Science magazine's capacity to identify and promote significant advances. Evolving digital publishing technologies play a crucial role in advancing AAAS's global mission for science communication and benefitting humankind.
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