Department of Molecular and Cell Biology, and Institute for Systems Genomics, University of Connecticut, Storrs, CT 06269, USA.
Institut Curie, PSL Research University, CNRS, UMR 144, 26 rue d'Ulm, F-75005 Paris, France.
Curr Biol. 2021 Nov 22;31(22):R1491-R1504. doi: 10.1016/j.cub.2021.09.083.
The centromere performs a universally conserved function, to accurately partition genetic information upon cell division. Yet, centromeres are among the most rapidly evolving regions of the genome and are bound by a varying assortment of centromere-binding factors that are themselves highly divergent at the protein-sequence level. A common thread in most species is the dependence on the centromere-specific histone variant CENP-A for the specification of the centromere site. However, CENP-A is not universally required in all species or cell types, making the identification of a general mechanism for centromere specification challenging. In this review, we examine our current understanding of the mechanisms of centromere specification in CENP-A-dependent and independent systems, focusing primarily on recent work.
着丝粒执行普遍保守的功能,即在细胞分裂时准确分配遗传信息。然而,着丝粒是基因组中进化最快的区域之一,并且受到各种着丝粒结合因子的束缚,这些因子在蛋白质序列水平上本身就高度多样化。在大多数物种中,一个共同点是依赖着丝粒特异性组蛋白变体 CENP-A 来指定着丝粒位置。然而,并非所有物种或细胞类型都普遍需要 CENP-A,这使得确定一个普遍的着丝粒指定机制具有挑战性。在这篇综述中,我们检查了我们目前对 CENP-A 依赖和独立系统中着丝粒指定机制的理解,主要关注最近的工作。