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着丝粒的诞生。

The birth of the centromere.

作者信息

Villasante Alfredo, Méndez-Lago María, Abad José P, Montejo de Garcíni Esteban

机构信息

Centro de Biología Molecular Severo Ochoa, Universidad Autonoma de Madrid, Spain.

出版信息

Cell Cycle. 2007 Dec 1;6(23):2872-6. doi: 10.4161/cc.6.23.5047.

Abstract

The centromere is the region of the eukaryotic chromosome that determines kinetochore formation and sister chromatid cohesion. Centromeres interact with spindle microtubules to ensure chromatid segregation during mitosis and homologous chromosome segregation during meiosis I. In recent years, the overall organization of centromeres in several eukaryotic species has been described, yet the mechanisms of centromere definition remain elusive. Understanding the evolutionary origin of the centromere may well elucidate aspects of its function. With such intention, we hypothesize that centromeres were derived from telomeres during the evolution of the eukaryotic chromosome. We propose that the proto-eukaryotic cell could not have evolved a nucleus without concurrently evolving a new tubulin-based cytoskeleton, the microtubules and a specific chromosomal region that enabled the chromosome-microtubule interaction, the centromere. The repetitive nature of the subtelomeric regions that gave rise to the centromeres forced the concerted evolution of the centromeres. Although this implies the absence of a conserved primary sequence, a conserved centromere-specific structural motif could still exist and determine where in the chromosome the centromere is to be formed. To support the "centromeres-from-telomeres" hypothesis, we discuss several situations, in meiosis and mitosis, where telomeric regions took over centromeric roles. The recently discovered phenomenon of centromere repositioning is also discussed because it has revealed new insights into how neocentromeres evolve.

摘要

着丝粒是真核生物染色体上决定动粒形成和姐妹染色单体黏连的区域。着丝粒与纺锤体微管相互作用,以确保有丝分裂过程中染色单体的分离以及减数分裂I过程中同源染色体的分离。近年来,已经描述了几种真核生物物种着丝粒的整体组织情况,但其定义机制仍然难以捉摸。了解着丝粒的进化起源很可能会阐明其功能的各个方面。出于这样的目的,我们假设在真核生物染色体进化过程中着丝粒是从端粒衍生而来的。我们提出,原核细胞如果不同时进化出一种基于微管蛋白的新细胞骨架、微管以及一个能够实现染色体与微管相互作用的特定染色体区域(着丝粒),就不可能进化出细胞核。产生着丝粒的亚端粒区域的重复性质促使着丝粒协同进化。尽管这意味着不存在保守的一级序列,但可能仍然存在一个保守的着丝粒特异性结构基序,并决定着丝粒在染色体上的形成位置。为了支持“着丝粒源自端粒”这一假说,我们讨论了减数分裂和有丝分裂中的几种情况,即端粒区域承担了着丝粒的作用。还讨论了最近发现的着丝粒重新定位现象,因为它揭示了新着丝粒如何进化的新见解。

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