NUCKS1 (nuclear ubiquitous casein kinase and cyclin-dependent kinase substrate 1) is a chromatin-associated, vertebrate-specific, and multifunctional protein with a role in DNA damage signaling and repair. Previously, we have shown that NUCKS1 helps maintain homologous recombination (HR) DNA repair in human cells and functions as a tumor suppressor in mice. However, the mechanisms by which NUCKS1 positively impacts these processes had remained unclear. Here, we show that NUCKS1 physically and functionally interacts with the DNA motor protein RAD54. Upon exposure of human cells to DNA-damaging agents, NUCKS1 controls the resolution of RAD54 foci. In unperturbed cells, NUCKS1 prevents RAD54’s inappropriate engagement with RAD51AP1. In vitro, NUCKS1 stimulates the ATPase activity of RAD54 and the RAD51–RAD54-mediated strand invasion step during displacement loop formation. Taken together, our data demonstrate that the NUCKS1 protein is an important new regulator of the spatiotemporal events in HR.
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5 October 2020
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September 02 2020
NUCKS1 promotes RAD54 activity in homologous recombination DNA repair
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David G. Maranon
,
1
Environmental and Radiological Health Sciences, Colorado State University, Fort Collins, CO
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Neelam Sharma
,
1
Environmental and Radiological Health Sciences, Colorado State University, Fort Collins, CO
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Yuxin Huang
,
3
Department of Biochemistry and Structural Biology, University of Texas Health San Antonio, San Antonio, TX
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Platon Selemenakis
,
Platon Selemenakis
1
Environmental and Radiological Health Sciences, Colorado State University, Fort Collins, CO
2
Cell and Molecular Biology Graduate Program, Colorado State University, Fort Collins, CO
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Meiling Wang
,
Meiling Wang
3
Department of Biochemistry and Structural Biology, University of Texas Health San Antonio, San Antonio, TX
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Noelia Altina
,
Noelia Altina
1
Environmental and Radiological Health Sciences, Colorado State University, Fort Collins, CO
2
Cell and Molecular Biology Graduate Program, Colorado State University, Fort Collins, CO
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Weixing Zhao
,
3
Department of Biochemistry and Structural Biology, University of Texas Health San Antonio, San Antonio, TX
Weixing Zhao: zhaow2@uthscsa.edu
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Claudia Wiese
1
Environmental and Radiological Health Sciences, Colorado State University, Fort Collins, CO
2
Cell and Molecular Biology Graduate Program, Colorado State University, Fort Collins, CO
Correspondence to Claudia Wiese: claudia.wiese@colostate.edu
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David G. Maranon
1
Environmental and Radiological Health Sciences, Colorado State University, Fort Collins, CO
Neelam Sharma
1
Environmental and Radiological Health Sciences, Colorado State University, Fort Collins, CO
Yuxin Huang
3
Department of Biochemistry and Structural Biology, University of Texas Health San Antonio, San Antonio, TX
Platon Selemenakis
1
Environmental and Radiological Health Sciences, Colorado State University, Fort Collins, CO
2
Cell and Molecular Biology Graduate Program, Colorado State University, Fort Collins, CO
Meiling Wang
3
Department of Biochemistry and Structural Biology, University of Texas Health San Antonio, San Antonio, TX
Noelia Altina
1
Environmental and Radiological Health Sciences, Colorado State University, Fort Collins, CO
2
Cell and Molecular Biology Graduate Program, Colorado State University, Fort Collins, CO
Weixing Zhao
3
Department of Biochemistry and Structural Biology, University of Texas Health San Antonio, San Antonio, TX
Claudia Wiese
1
Environmental and Radiological Health Sciences, Colorado State University, Fort Collins, CO
2
Cell and Molecular Biology Graduate Program, Colorado State University, Fort Collins, CO
Correspondence to Claudia Wiese: claudia.wiese@colostate.edu
Weixing Zhao: zhaow2@uthscsa.edu
*
D.G. Maranon, N. Sharma, and Y. Huang contributed equally to this paper.
Received:
December 04 2019
Revision Received:
May 04 2020
Accepted:
June 18 2020
Online Issn: 1540-8140
Print Issn: 0021-9525
Funding:
Max and Minnie Tomerlin Voelcker Fund
(NO AWARD)
National Institutes of Health
(ES021454, ES029206)
V Foundation for Cancer Research
(V2019.Q13)
© 2020 Maranon et al.
2020
This article is distributed under the terms of an Attribution–Noncommercial–Share Alike–No Mirror Sites license for the first six months after the publication date (see http://www.rupress.org/terms/). After six months it is available under a Creative Commons License (Attribution–Noncommercial–Share Alike 4.0 International license, as described at https://creativecommons.org/licenses/by-nc-sa/4.0/).
J Cell Biol (2020) 219 (10): e201911049.
Article history
Received:
December 04 2019
Revision Received:
May 04 2020
Accepted:
June 18 2020
Citation
David G. Maranon, Neelam Sharma, Yuxin Huang, Platon Selemenakis, Meiling Wang, Noelia Altina, Weixing Zhao, Claudia Wiese; NUCKS1 promotes RAD54 activity in homologous recombination DNA repair. J Cell Biol 5 October 2020; 219 (10): e201911049. doi: https://doi.org/10.1083/jcb.201911049
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