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凝缩蛋白缺失的有丝分裂染色体中揭示的基因组折叠原理。

Genome folding principles revealed in condensin-depleted mitotic chromosomes.

作者信息

Zhao Han, Lin Yinzhi, Lin En, Liu Fuhai, Shu Lirong, Jing Dannan, Wang Baiyue, Wang Manzhu, Shan Fengnian, Zhang Lin, Lam Jessica C, Midla Susannah C, Giardine Belinda M, Keller Cheryl A, Hardison Ross C, Blobel Gerd A, Zhang Haoyue

机构信息

Institute of Molecular Physiology, Shenzhen Bay Laboratory, Shenzhen, Guangdong, China.

Department of Biology, College of Science, Shantou University, Shantou, China.

出版信息

bioRxiv. 2023 Nov 13:2023.11.09.566494. doi: 10.1101/2023.11.09.566494.

Abstract

During mitosis, condensin activity interferes with interphase chromatin structures. Here, we generated condensin-free mitotic chromosomes to investigate genome folding principles. Co-depletion of condensin I and II, but neither alone, triggered mitotic chromosome compartmentalization in ways that differ from interphase. Two distinct euchromatic compartments, indistinguishable in interphase, rapidly emerged upon condensin loss with different interaction preferences and dependence on H3K27ac. Constitutive heterochromatin gradually self-aggregated and co-compartmentalized with the facultative heterochromatin, contrasting with their separation during interphase. While topologically associating domains (TADs) and CTCF/cohesin mediated structural loops remained undetectable, cis-regulatory element contacts became apparent, providing an explanation for their quick re-establishment during mitotic exit. HP1 proteins, which are thought to partition constitutive heterochromatin, were absent from mitotic chromosomes, suggesting, surprisingly, that constitutive heterochromatin can self-aggregate without HP1. Indeed, in cells traversing from M- to G1-phase in the combined absence of HP1α, HP1β and HP1γ, re-established constitutive heterochromatin compartments normally. In sum, "clean-slate" condensing-deficient mitotic chromosomes illuminate mechanisms of genome compartmentalization not revealed in interphase cells.

摘要

在有丝分裂过程中,凝聚素活性会干扰间期染色质结构。在此,我们生成了不含凝聚素的有丝分裂染色体,以研究基因组折叠原理。凝聚素 I 和凝聚素 II 的共同缺失而非单独缺失,以不同于间期的方式引发了有丝分裂染色体的区室化。两种在间期无法区分的不同常染色质区室,在凝聚素缺失后迅速出现,具有不同的相互作用偏好且依赖于 H3K27ac。组成型异染色质逐渐自我聚集,并与兼性异染色质共同区室化,这与它们在间期的分离形成对比。虽然拓扑相关结构域(TADs)和 CTCF/黏连蛋白介导的结构环仍然无法检测到,但顺式调控元件接触变得明显,这为它们在有丝分裂退出过程中的快速重新建立提供了解释。有丝分裂染色体中不存在被认为可划分组成型异染色质的 HP1 蛋白,令人惊讶的是,这表明组成型异染色质可以在没有 HP1 的情况下自我聚集。事实上,在同时缺失 HP1α、HP1β 和 HP1γ 的情况下从 M 期过渡到 G1 期的细胞中,重新建立的组成型异染色质区室正常。总之,“白板”状的凝聚缺陷型有丝分裂染色体揭示了间期细胞中未揭示的基因组区室化机制。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1c7c/10680603/847b1b6cd8bd/nihpp-2023.11.09.566494v1-f0007.jpg

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