{"title":"CCAN forms the spherical shell-like structure in interphase kinetochores","authors":"Yuji Sakai, Mariko Ariyoshi, Yasuhiro Hirano, Yutaka Mahana, Aussie Suzuki, Toru Hirota, Masashi Tachikawa, Tatsuo Fukagawa","doi":"10.1126/sciadv.aef4365","DOIUrl":null,"url":null,"abstract":"<div >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.</div>","PeriodicalId":21609,"journal":{"name":"Science Advances","volume":"12 43","pages":""},"PeriodicalIF":13.9000,"publicationDate":"2026-10-21","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.science.org/doi/reader/10.1126/sciadv.aef4365","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Science Advances","FirstCategoryId":"103","ListUrlMain":"https://www.science.org/doi/10.1126/sciadv.aef4365","RegionNum":1,"RegionCategory":"综合性期刊","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"MULTIDISCIPLINARY SCIENCES","Score":null,"Total":0}
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.
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.