ANKLE1 processes chromatin bridges by cleaving mechanically stressed DNA

Chromatin bridges experience significant tension due to spindle fiber pulling and cell migration. Uncontrolled breakage of chromatin bridges by actomyosin contractile forces leads to detrimental consequences. The existence of specialized mechanisms that process chromatin bridges to prevent catastrophic rupture remains uncertain. Here, we uncover a unique property of ANKLE1, a midbody-tethered endonuclease implicated in chromatin bridge processing, in sensing and responding to DNA tension and supercoiling during cell division. Using single-molecule analyses, we found that ANKLE1 specifically cuts supercoiled or mechanically stretched DNA. At higher stretching forces, ANKLE1 cleaves both strands of negatively supercoiled DNA, mirroring conditions in which stretched chromatin bridges lose histones to expose negatively supercoiled DNA. These findings show that ANKLE1 acts as a DNA tension sensor that resolves stretched chromatin bridges. Our study highlights the significance of mechanical forces in DNA bridge processing, enhances our understanding of how cells preserve genome integrity during cell division.

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Publication Details

Journal
Nature Communications
Published
2025-12-08
DOI
https://doi.org/10.1038/s41467-025-65905-7
Citations
1
Primary Topic
Genomics and Chromatin Dynamics
Type
article
Field-Weighted Citation Impact
0.81

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article

ANKLE1 processes chromatin bridges by cleaving mechanically stressed DNA

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1 citations
Nature Communications
Genomics and Chromatin Dynamics
0.81
article

ANKLE1 processes chromatin bridges by cleaving mechanically stressed DNA

Stephen C. West, Huadong Jiang, Artem K. Efremov, Jie Long, Nannan Kong, Ying Wai Chan, Yuanliang Zhai, Rajvee Shah Punatar, Fei He, Zhichun Xu, Yu Ching Poon
article en
1 citations

Abstract

Chromatin bridges experience significant tension due to spindle fiber pulling and cell migration. Uncontrolled breakage of chromatin bridges by actomyosin contractile forces leads to detrimental consequences. The existence of specialized mechanisms that process chromatin bridges to prevent catastrophic rupture remains uncertain. Here, we uncover a unique property of ANKLE1, a midbody-tethered endonuclease implicated in chromatin bridge processing, in sensing and responding to DNA tension and supercoiling during cell division. Using single-molecule analyses, we found that ANKLE1 specifically cuts supercoiled or mechanically stretched DNA. At higher stretching forces, ANKLE1 cleaves both strands of negatively supercoiled DNA, mirroring conditions in which stretched chromatin bridges lose histones to expose negatively supercoiled DNA. These findings show that ANKLE1 acts as a DNA tension sensor that resolves stretched chromatin bridges. Our study highlights the significance of mechanical forces in DNA bridge processing, enhances our understanding of how cells preserve genome integrity during cell division.

Nature CommunicationsVol. 16(1)
Hong Kong University of Science and Technology (HK), The Francis Crick Institute (GB), Shenzhen Bay Laboratory (CN), University of Hong Kong (HK)
Wellcome Trust, Francis Crick Institute, Cancer Research UK, National University of Singapore, Louis-Jeantet Foundation, Shenzhen Bay Laboratory, Medical Research Council
Openalex Percentile: Top 21%
Genomics and Chromatin Dynamics
0.81
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