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减数分裂同源染色体配对的机制。

The mechanism of meiotic homologue pairing.

作者信息

Maguire M P

出版信息

J Theor Biol. 1984 Feb 21;106(4):605-15. doi: 10.1016/0022-5193(84)90010-9.

Abstract

Homologous chromosome pairing involves the moving together of matching chromosomes or chromosome segments across substantial distances within a nucleus. Although the time in the life cycle of initial association of homologues varies among organisms, it may well be that similar underlying mechanisms for its occurrence prevail throughout sexually reproducing eukaryotes. The means by which pairing its accomplished is in no case understood. In the apparent absence of a long range specific force of attraction, simple partial models have been proposed which relay for the most part upon interactions of chromosome ends (telomeres) with specialized portions of the nuclear envelope. While such interactions, as well as the persistence of chromosome orientation established by mitotic anaphase poleward movement of centromere regions, may provide in many cases for closer than random positioning of some parts of homologues, the distances remaining to be traversed are still long range in physical-chemical terms. Also, the specific pairing observed in some kinds of rearranged segments is not facilitated by such circumstances, even if synapsis is initiated at available homologous telomere pairs and proceeds to completion by a "zip-up" process. A unified, more complex model is considered which is designed to accommodate the various relevant findings. It invokes the interaction of intranuclear structures with intercalary and/or terminal chromosomal pairing sites, e.g. filamentous structures which specifically bind to these, and a contractile system involving proteins such as actin and myosin to draw homologues together.

摘要

同源染色体配对涉及到匹配的染色体或染色体片段在细胞核内跨越相当大的距离移动到一起。尽管同源染色体初次关联在生命周期中的时间在不同生物体中有所不同,但很可能在所有有性生殖的真核生物中,其发生的潜在机制相似。然而,配对完成的方式却完全不为人所知。在明显缺乏远距离特异性吸引力的情况下,已经提出了一些简单的局部模型,这些模型在很大程度上依赖于染色体末端(端粒)与核膜特定部分的相互作用。虽然这种相互作用,以及由着丝粒区域在有丝分裂后期向极移动所建立的染色体取向的持续性,在许多情况下可能使同源染色体的某些部分比随机定位更靠近,但从物理化学角度来看,仍有很长的距离需要跨越。此外,即使联会在可用的同源端粒对处启动并通过“拉链式”过程完成,在某些重排片段中观察到的特异性配对也不会因这种情况而变得更容易。本文考虑了一个统一的、更复杂的模型,该模型旨在适应各种相关发现。它涉及核内结构与居间和/或末端染色体配对位点的相互作用,例如与这些位点特异性结合的丝状结构,以及一个涉及肌动蛋白和肌球蛋白等蛋白质的收缩系统,以将同源染色体拉到一起。

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