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A novel motif of Rad51 serves as an interaction hub for recombination auxiliary factors

Homologous recombination (HR) is essential for maintaining genome stability. Although Rad51 is the key protein that drives HR, multiple auxiliary factors interact with Rad51 to potentiate its activity. Here, we present an interdisciplinary characterization of the interactions between Rad51 and these...

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Autores principales: Afshar, Negar, Argunhan, Bilge, Palihati, Maierdan, Taniguchi, Goki, Tsubouchi, Hideo, Iwasaki, Hiroshi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: eLife Sciences Publications, Ltd 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7837696/
https://www.ncbi.nlm.nih.gov/pubmed/33493431
http://dx.doi.org/10.7554/eLife.64131
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author Afshar, Negar
Argunhan, Bilge
Palihati, Maierdan
Taniguchi, Goki
Tsubouchi, Hideo
Iwasaki, Hiroshi
author_facet Afshar, Negar
Argunhan, Bilge
Palihati, Maierdan
Taniguchi, Goki
Tsubouchi, Hideo
Iwasaki, Hiroshi
author_sort Afshar, Negar
collection PubMed
description Homologous recombination (HR) is essential for maintaining genome stability. Although Rad51 is the key protein that drives HR, multiple auxiliary factors interact with Rad51 to potentiate its activity. Here, we present an interdisciplinary characterization of the interactions between Rad51 and these factors. Through structural analysis, we identified an evolutionarily conserved acidic patch of Rad51. The neutralization of this patch completely abolished recombinational DNA repair due to defects in the recruitment of Rad51 to DNA damage sites. This acidic patch was found to be important for the interaction with Rad55-Rad57 and essential for the interaction with Rad52. Furthermore, biochemical reconstitutions demonstrated that neutralization of this acidic patch also impaired the interaction with Rad54, indicating that a single motif is important for the interaction with multiple auxiliary factors. We propose that this patch is a fundamental motif that facilitates interactions with auxiliary factors and is therefore essential for recombinational DNA repair.
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spelling pubmed-78376962021-01-27 A novel motif of Rad51 serves as an interaction hub for recombination auxiliary factors Afshar, Negar Argunhan, Bilge Palihati, Maierdan Taniguchi, Goki Tsubouchi, Hideo Iwasaki, Hiroshi eLife Biochemistry and Chemical Biology Homologous recombination (HR) is essential for maintaining genome stability. Although Rad51 is the key protein that drives HR, multiple auxiliary factors interact with Rad51 to potentiate its activity. Here, we present an interdisciplinary characterization of the interactions between Rad51 and these factors. Through structural analysis, we identified an evolutionarily conserved acidic patch of Rad51. The neutralization of this patch completely abolished recombinational DNA repair due to defects in the recruitment of Rad51 to DNA damage sites. This acidic patch was found to be important for the interaction with Rad55-Rad57 and essential for the interaction with Rad52. Furthermore, biochemical reconstitutions demonstrated that neutralization of this acidic patch also impaired the interaction with Rad54, indicating that a single motif is important for the interaction with multiple auxiliary factors. We propose that this patch is a fundamental motif that facilitates interactions with auxiliary factors and is therefore essential for recombinational DNA repair. eLife Sciences Publications, Ltd 2021-01-25 /pmc/articles/PMC7837696/ /pubmed/33493431 http://dx.doi.org/10.7554/eLife.64131 Text en © 2021, Afshar et al http://creativecommons.org/licenses/by/4.0/ http://creativecommons.org/licenses/by/4.0/This article is distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use and redistribution provided that the original author and source are credited.
spellingShingle Biochemistry and Chemical Biology
Afshar, Negar
Argunhan, Bilge
Palihati, Maierdan
Taniguchi, Goki
Tsubouchi, Hideo
Iwasaki, Hiroshi
A novel motif of Rad51 serves as an interaction hub for recombination auxiliary factors
title A novel motif of Rad51 serves as an interaction hub for recombination auxiliary factors
title_full A novel motif of Rad51 serves as an interaction hub for recombination auxiliary factors
title_fullStr A novel motif of Rad51 serves as an interaction hub for recombination auxiliary factors
title_full_unstemmed A novel motif of Rad51 serves as an interaction hub for recombination auxiliary factors
title_short A novel motif of Rad51 serves as an interaction hub for recombination auxiliary factors
title_sort novel motif of rad51 serves as an interaction hub for recombination auxiliary factors
topic Biochemistry and Chemical Biology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7837696/
https://www.ncbi.nlm.nih.gov/pubmed/33493431
http://dx.doi.org/10.7554/eLife.64131
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