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构建着丝粒:从基础蛋白到三维结构

Building the centromere: from foundation proteins to 3D organization.

作者信息

Amor David J, Kalitsis Paul, Sumer Huseyin, Choo K H Andy

机构信息

Murdoch Childrens Research Institute, Royal Children's Hospital, Flemington Road, Parkville, Melbourne, Victoria 3052, Australia.

出版信息

Trends Cell Biol. 2004 Jul;14(7):359-68. doi: 10.1016/j.tcb.2004.05.009.

Abstract

At each mitosis, accurate segregation of every chromosome is ensured by the assembly of a kinetochore at each centromeric locus. Six foundation kinetochore proteins that assemble hierarchically and co-dependently have been identified in vertebrates. CENP-A, Mis12, CENP-C, CENP-H and CENP-I localize to a core domain of centromeric chromatin. The sixth protein, CENP-B, although not essential in higher eukaryotes, has homologues in fission yeast that bind pericentric DNA and are essential for heterochromatin formation. Foundation kinetochore proteins have various roles and mutual interactions, and their associations with centromeric DNA and heterochromatin create structural domains that support the different functions of the centromere. Advances in molecular and microscopic techniques, coupled with rare centromere variants, have enabled us to gain fresh insights into the linear and 3D organization of centromeric chromatin.

摘要

在每次有丝分裂过程中,通过在每个着丝粒位点组装动粒来确保每条染色体的精确分离。在脊椎动物中已鉴定出六种分层组装且相互依赖的基础动粒蛋白。CENP-A、Mis12、CENP-C、CENP-H和CENP-I定位于着丝粒染色质的核心结构域。第六种蛋白CENP-B虽然在高等真核生物中并非必需,但在裂殖酵母中有同源物,可结合着丝粒周围DNA,对异染色质形成至关重要。基础动粒蛋白具有多种作用和相互作用,它们与着丝粒DNA和异染色质的结合形成了支持着丝粒不同功能的结构域。分子和显微镜技术的进步,再加上罕见的着丝粒变异体,使我们能够对着丝粒染色质的线性和三维组织有新的认识。

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