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真细菌的基因组折叠成 SMC 依赖的环和域,但缺乏转录介导的分隔化。

Euryarchaeal genomes are folded into SMC-dependent loops and domains, but lack transcription-mediated compartmentalization.

机构信息

Institut Pasteur, Unité Régulation Spatiale des Génomes, CNRS UMR 3525, 75015 Paris, France.

Université Paris-Saclay, CEA, CNRS, Institute for Integrative Biology of the Cell (I2BC), 91198, Gif-sur-Yvette, France.

出版信息

Mol Cell. 2021 Feb 4;81(3):459-472.e10. doi: 10.1016/j.molcel.2020.12.013. Epub 2020 Dec 30.

DOI:10.1016/j.molcel.2020.12.013
PMID:33382984
Abstract

Hi-C has become a routine method for probing the 3D organization of genomes. However, when applied to prokaryotes and archaea, the current protocols are expensive and limited in their resolution. We develop a cost-effective Hi-C protocol to explore chromosome conformations of these two kingdoms at the gene or operon level. We first validate it on E. coli and V. cholera, generating sub-kilobase-resolution contact maps, and then apply it to the euryarchaeota H. volcanii, Hbt. salinarum, and T. kodakaraensis. With a resolution of up to 1 kb, we explore the diversity of chromosome folding in this phylum. In contrast to crenarchaeota, these euryarchaeota lack (active/inactive) compartment-like structures. Instead, their genomes are composed of self-interacting domains and chromatin loops. In H. volcanii, these structures are regulated by transcription and the archaeal structural maintenance of chromosomes (SMC) protein, further supporting the ubiquitous role of these processes in shaping the higher-order organization of genomes.

摘要

Hi-C 已成为研究基因组 3D 结构的常规方法。然而,当应用于原核生物和古菌时,目前的方法既昂贵又限制了其分辨率。我们开发了一种具有成本效益的 Hi-C 方案,以在基因或操纵子水平上探索这两个领域的染色体构象。我们首先在大肠杆菌和霍乱弧菌上验证了该方案,生成了亚千碱基分辨率的接触图谱,然后将其应用于广古菌的 H. volcanii、Hbt. salinarum 和 T. kodakaraensis。分辨率高达 1 kb,我们探索了该门中染色体折叠的多样性。与泉古菌不同,这些广古菌缺乏(活跃/不活跃)类似隔室的结构。相反,它们的基因组由自我相互作用的结构域和染色质环组成。在 H. volcanii 中,这些结构受转录和古菌结构维持染色体(SMC)蛋白的调节,进一步支持这些过程在塑造基因组的高级结构中的普遍作用。

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