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Homologous Pairing Activities of Two Rice RAD51 Proteins, RAD51A1 and RAD51A2
In higher eukaryotes, RAD51 functions as an essential protein in homologous recombination and recombinational repair of DNA double strand breaks. During these processes, RAD51 catalyzes homologous pairing between single-stranded DNA and double-stranded DNA. Japonica cultivars of rice (Oryza sativa)...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3790826/ https://www.ncbi.nlm.nih.gov/pubmed/24124491 http://dx.doi.org/10.1371/journal.pone.0075451 |
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author | Morozumi, Yuichi Ino, Ryohei Ikawa, Shukuko Mimida, Naozumi Shimizu, Takeshi Toki, Seiichi Ichikawa, Hiroaki Shibata, Takehiko Kurumizaka, Hitoshi |
author_facet | Morozumi, Yuichi Ino, Ryohei Ikawa, Shukuko Mimida, Naozumi Shimizu, Takeshi Toki, Seiichi Ichikawa, Hiroaki Shibata, Takehiko Kurumizaka, Hitoshi |
author_sort | Morozumi, Yuichi |
collection | PubMed |
description | In higher eukaryotes, RAD51 functions as an essential protein in homologous recombination and recombinational repair of DNA double strand breaks. During these processes, RAD51 catalyzes homologous pairing between single-stranded DNA and double-stranded DNA. Japonica cultivars of rice (Oryza sativa) encode two RAD51 proteins, RAD51A1 and RAD51A2, whereas only one RAD51 exists in yeast and mammals. However, the functional differences between RAD51A1 and RAD51A2 have not been elucidated, because their biochemical properties have not been characterized. In the present study, we purified RAD51A1 and RAD51A2, and found that RAD51A2 robustly promotes homologous pairing in vitro. RAD51A1 also possesses homologous-pairing activity, but it is only about 10% of the RAD51A2 activity. Both RAD51A1 and RAD51A2 bind to ssDNA and dsDNA, and their DNA binding strictly requires ATP, which modulates the polymer formation activities of RAD51A1 and RAD51A2. These findings suggest that although both RAD51A1 and RAD51A2 have the potential to catalyze homologous pairing, RAD51A2 may be the major recombinase in rice. |
format | Online Article Text |
id | pubmed-3790826 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-37908262013-10-11 Homologous Pairing Activities of Two Rice RAD51 Proteins, RAD51A1 and RAD51A2 Morozumi, Yuichi Ino, Ryohei Ikawa, Shukuko Mimida, Naozumi Shimizu, Takeshi Toki, Seiichi Ichikawa, Hiroaki Shibata, Takehiko Kurumizaka, Hitoshi PLoS One Research Article In higher eukaryotes, RAD51 functions as an essential protein in homologous recombination and recombinational repair of DNA double strand breaks. During these processes, RAD51 catalyzes homologous pairing between single-stranded DNA and double-stranded DNA. Japonica cultivars of rice (Oryza sativa) encode two RAD51 proteins, RAD51A1 and RAD51A2, whereas only one RAD51 exists in yeast and mammals. However, the functional differences between RAD51A1 and RAD51A2 have not been elucidated, because their biochemical properties have not been characterized. In the present study, we purified RAD51A1 and RAD51A2, and found that RAD51A2 robustly promotes homologous pairing in vitro. RAD51A1 also possesses homologous-pairing activity, but it is only about 10% of the RAD51A2 activity. Both RAD51A1 and RAD51A2 bind to ssDNA and dsDNA, and their DNA binding strictly requires ATP, which modulates the polymer formation activities of RAD51A1 and RAD51A2. These findings suggest that although both RAD51A1 and RAD51A2 have the potential to catalyze homologous pairing, RAD51A2 may be the major recombinase in rice. Public Library of Science 2013-10-04 /pmc/articles/PMC3790826/ /pubmed/24124491 http://dx.doi.org/10.1371/journal.pone.0075451 Text en © 2013 Morozumi et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited. |
spellingShingle | Research Article Morozumi, Yuichi Ino, Ryohei Ikawa, Shukuko Mimida, Naozumi Shimizu, Takeshi Toki, Seiichi Ichikawa, Hiroaki Shibata, Takehiko Kurumizaka, Hitoshi Homologous Pairing Activities of Two Rice RAD51 Proteins, RAD51A1 and RAD51A2 |
title | Homologous Pairing Activities of Two Rice RAD51 Proteins, RAD51A1 and RAD51A2 |
title_full | Homologous Pairing Activities of Two Rice RAD51 Proteins, RAD51A1 and RAD51A2 |
title_fullStr | Homologous Pairing Activities of Two Rice RAD51 Proteins, RAD51A1 and RAD51A2 |
title_full_unstemmed | Homologous Pairing Activities of Two Rice RAD51 Proteins, RAD51A1 and RAD51A2 |
title_short | Homologous Pairing Activities of Two Rice RAD51 Proteins, RAD51A1 and RAD51A2 |
title_sort | homologous pairing activities of two rice rad51 proteins, rad51a1 and rad51a2 |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3790826/ https://www.ncbi.nlm.nih.gov/pubmed/24124491 http://dx.doi.org/10.1371/journal.pone.0075451 |
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