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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...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
eLife Sciences Publications, Ltd
2021
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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. |
format | Online Article Text |
id | pubmed-7837696 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | eLife Sciences Publications, Ltd |
record_format | MEDLINE/PubMed |
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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