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环挤压规则:新一代

Loop extrusion rules: the next generation.

作者信息

Corsi Flavia, Rusch Emma, Goloborodko Anton

机构信息

Institute of Molecular Biotechnology, Dr. Bohr-Gasse 3, 1030 Vienna, Austria. Electronic address: https://twitter.com/@flavia_corsi.

Institute of Molecular Biotechnology, Dr. Bohr-Gasse 3, 1030 Vienna, Austria. Electronic address: https://twitter.com/@emma__rush.

出版信息

Curr Opin Genet Dev. 2023 Aug;81:102061. doi: 10.1016/j.gde.2023.102061. Epub 2023 Jun 22.

Abstract

The interphase genome of vertebrates contains roughly 100 000 dynamic loops formed by cohesins. These loops are thought to play important roles in many functions, but their exact contribution in each case remains hotly disputed. The key challenge in studying these loops is the lack of a single experimental technique that could reliably and comprehensively visualize their locations and dynamics. Yet, we can infer them using theoretical models that integrate complementary experimental observations. Modeling proved instrumental in showing that cohesins form loops via extrusion. The loop extrusion model made numerous successful qualitative and quantitative predictions and inspired many experiments. However, it also demonstrated limited accuracy in predicting contact maps. Recent research suggests that the original model did not fully account for the intricate details of the mechanism of loop extrusion and its complex regulation. Here, we review the progress in visualizing extrusion and characterizing the cohesin cofactors. These discoveries can be summarized as 'rules' of cohesin movement along chromosomes and incorporated into the next generation of models. Such improved models will enable more accurate inferences of positions and dynamics of cohesin loops and generate better predictions for designing experiments.

摘要

脊椎动物的间期基因组包含由黏连蛋白形成的约10万个动态环。这些环被认为在许多功能中发挥重要作用,但它们在每种情况下的确切贡献仍存在激烈争议。研究这些环的关键挑战在于缺乏一种能够可靠且全面地可视化其位置和动态的单一实验技术。然而,我们可以使用整合了互补实验观察结果的理论模型来推断它们。建模被证明有助于表明黏连蛋白通过挤压形成环。环挤压模型做出了许多成功的定性和定量预测,并激发了许多实验。然而,它在预测接触图谱方面也显示出有限的准确性。最近的研究表明,原始模型没有充分考虑环挤压机制及其复杂调控的复杂细节。在这里,我们回顾了在可视化挤压和表征黏连蛋白辅助因子方面的进展。这些发现可以总结为黏连蛋白沿染色体移动的“规则”,并纳入下一代模型中。这种改进的模型将能够更准确地推断黏连蛋白环的位置和动态,并为设计实验产生更好的预测。

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