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基于 condensin 和拓扑异构酶 II 相互作用的染色体浓缩模型。

A model for chromosome condensation based on the interplay between condensin and topoisomerase II.

机构信息

Genome Damage and Stability Centre, Science Park Road, University of Sussex, Falmer, Brighton, East Sussex, BN1 9RQ, UK.

出版信息

Trends Genet. 2012 Mar;28(3):110-7. doi: 10.1016/j.tig.2011.11.004. Epub 2012 Jan 10.

Abstract

The compaction of chromatin that occurs when cells enter mitosis is probably the most iconic process of dividing cells. Mitotic chromosomal compaction or 'condensation' is functionally linked to resolution of chromosomal intertwines, transcriptional shut-off and complete segregation of chromosomes. At present, understanding of the molecular events required to convert interphase chromatin into mitotic chromosomes is limited. Here, we review recent advances in the field, focusing on potential chromosomal compaction mechanisms and their importance to chromosome segregation. We propose a model of how metaphase chromosomes could be shaped based on the enzymatic activities of condensin and topoisomerase II in overwinding and relaxation of the DNA fiber during mitosis. We suggest that condensin overwinding is an important requirement for intertwine resolution by topoisomerase II and, together with the inhibition of transcription, contributes to cytological mitotic chromosome appearance or 'condensation'.

摘要

当细胞进入有丝分裂时,染色质的压缩可能是分裂细胞最具标志性的过程。有丝分裂染色体的压缩或“凝聚”与染色体缠绕的解决、转录关闭和染色体完全分离在功能上相关联。目前,对于将间期染色质转化为有丝分裂染色体所需的分子事件的理解是有限的。在这里,我们回顾了该领域的最新进展,重点关注潜在的染色体压缩机制及其对染色体分离的重要性。我们提出了一种基于有丝分裂过程中凝聚蛋白和拓扑异构酶 II 对 DNA 纤维的过度缠绕和松弛的酶活性来塑造中期染色体的模型。我们认为,拓扑异构酶 II 解开缠绕需要凝聚蛋白的过度缠绕,并且与转录抑制一起,有助于细胞学有丝分裂染色体的出现或“凝聚”。

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