Fork coupling directs DNA replication elongation and termination

Author:

Liu Yang12ORCID,Zhangding Zhengrong1ORCID,Liu Xuhao1ORCID,Gan Tingting123ORCID,Ai Chen12,Wu Jinchun12,Liang Haoxin1,Chen Mohan1,Guo Yuefeng1ORCID,Lu Rusen12,Jiang Yongpeng12,Ji Xiong12,Gao Ning24ORCID,Kong Daochun25,Li Qing25ORCID,Hu Jiazhi123ORCID

Affiliation:

1. The MOE Key Laboratory of Cell Proliferation and Differentiation, School of Life Sciences, Genome Editing Research Center, Peking University; Beijing 100871, China.

2. PKU-THU Center for Life Sciences, Peking University, Beijing 100871, China.

3. Peking University ChengDu Academy for Advanced Interdisciplinary Biotechnologies, Chengdu, Sichuan 610213, China.

4. State Key Laboratory of Membrane Biology, School of Life Sciences, Peking University, Beijing 100871, China.

5. State Key Laboratory of Protein and Plant Gene Research, School of Life Sciences, Peking University, Beijing 100871, China.

Abstract

DNA replication is initiated at multiple loci to ensure timely duplication of eukaryotic genomes. Sister replication forks progress bidirectionally, and replication terminates when two convergent forks encounter one another. To investigate the coordination of replication forks, we developed a replication-associated in situ HiC method to capture chromatin interactions involving nascent DNA. We identify more than 2000 fountain-like structures of chromatin contacts in human and mouse genomes, indicative of coupling of DNA replication forks. Replication fork interaction not only occurs between sister forks but also involves forks from two distinct origins to predetermine replication termination. Termination-associated chromatin fountains are sensitive to replication stress and lead to coupled forks–associated genomic deletions in cancers. These findings reveal the spatial organization of DNA replication forks within the chromatin context.

Publisher

American Association for the Advancement of Science (AAAS)

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