An archaeal chromatin protein condenses DNA through bridging-induced phase separation

Author:

Zhang Zhenfeng1,Ding Niannian2,Wang Mengxue2,Li Haodun2,Sun Fei3,Chen Yuanyuan4,Yang Yunfeng5,Zhang Yi3,Huang Junkai2,Dai Xin2,Shen Yulong6ORCID,Fu Yu7ORCID,Huang Li8

Affiliation:

1. Institute of Microbiology, Chinese Academy of Sciences

2. Institute of Microbiology,Chinese Academy of Sciences

3. School of Life Science and Technology, Southeast University

4. Institute of Biophysics, Chinese Academy of Sciences

5. Institute and State Key Laboratory of Microbial Technology, Shandong University

6. Shandong University

7. State Key Laboratory of Microbial Resources, Institute of Microbiology Chinese Academy of Sciences

8. State Key Laboratory of Microbial Resources, Institute of Microbiology, Chinese Academy of Sciences

Abstract

Abstract Phase separation serves an important role in the three-dimensional chromosome organization and remodeling in eukaryotes. Whether this process is involved in archaeal chromosome organization is unknown. Here we demonstrate that archaeal DNA condensing protein1 (aDCP1) from the hyperthermophilic crenarchaeon Sulfolobus islandicus is able to bridge DNA efficiently and form large protein-DNA condensates with a droplet- or gel-like morphology in vitro. Within the condensates, aDCP1 exhibits a fast dynamic while the DNA appears in a solid-like state. At the single-molecule level, aDCP1 efficiently compacts DNA through a three-step mechanism, which presumably entails the clustering of aDCP1 on the DNA and the subsequent fusion of the clusters. Deletion of the aDCP1 gene results in noticeable changes in chromosome conformation in S. islandicus, which are characterized by enhanced interactions between the A and B compartments and reduced interactions within the self-interacting domains as well as between domains in the same compartment. Taken together, our results indicate that aDCP1 is capable of inducing DNA bridging-induced phase separation and serves a role in chromosome organization in the organism.

Publisher

Research Square Platform LLC

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