DNA环挤压SMC蛋白复合物的结构-功能关系

BIODESIGN Pub Date : 2021-03-30 DOI:10.34184/KSSB.2021.9.1.1
Hansol Lee, H. Noh, Je-Kyung Ryu
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引用次数: 4

摘要

染色体复合体的结构维持对染色体的组织至关重要。它们挤出DNA环,将2米长的DNA压缩成一个微米大小的染色体结构。DNA环挤压过程被认为是SMC复合物时空染色体组织的普遍机制,从原核生物到真核生物几乎所有物种都保守存在。然而,SMC配合物挤压DNA环的分子机制仍存在争议;人们提出了各种初步的机制模型,但没有明确的共识。本文综述了从原核生物到真核生物的各种SMC复合物的结构研究,以了解SMC复合物参与DNA环挤压的结构功能关系。我们在先前的报道的基础上介绍了对SMC复合物构象的有争议的观察,并讨论了通过对不同SMC复合物构象的实验观察提出的DNA环挤压的各种机制。p1 -13迷你审查https://doi.org/10.34184/kssb.2021.9.1.1
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Structure-function relationships of SMC protein complexes for DNA loop extrusion
Structural Maintenance of Chromosome (SMC) complexes are vital for chromosome organization. They extrude DNA loops to compact 2 meters of DNA into a micrometer-sized chromosome structure. The DNA loop extrusion process is believed to be a universal mechanism of SMC complexes for spatiotemporal chromosome organization conserved in almost all species from prokaryotes to eukaryotes. However, the molecular mechanism of DNA loop extrusion by SMC complexes is under debate; various tentative mechanistic models have been suggested, but there is no clear consensus. Here, we review the structural studies of various SMC complexes from prokaryotes to eukaryotes to understand the structurefunction relationships of SMC complexes involved in DNA loop extrusion. We introduce controversial observations of the conformations of SMC complexes based on previous reports and discuss various proposed mechanisms of DNA loop extrusion suggested by experimental observations of the conformations of diverse SMC complexes. P 1-13 MINI REVIEW https://doi.org/10.34184/kssb.2021.9.1.1
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