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DIDS, a chemical compound that inhibits RAD51-mediated homologous pairing and strand exchange
RAD51, an essential eukaryotic DNA recombinase, promotes homologous pairing and strand exchange during homologous recombination and the recombinational repair of double strand breaks. Mutations that up- or down-regulate RAD51 gene expression have been identified in several tumors, suggesting that in...
Autores principales: | , , , , , , , , |
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Formato: | Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2009
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2691838/ https://www.ncbi.nlm.nih.gov/pubmed/19336413 http://dx.doi.org/10.1093/nar/gkp200 |
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author | Ishida, Takako Takizawa, Yoshimasa Kainuma, Takashi Inoue, Jin Mikawa, Tsutomu Shibata, Takehiko Suzuki, Hidekazu Tashiro, Satoshi Kurumizaka, Hitoshi |
author_facet | Ishida, Takako Takizawa, Yoshimasa Kainuma, Takashi Inoue, Jin Mikawa, Tsutomu Shibata, Takehiko Suzuki, Hidekazu Tashiro, Satoshi Kurumizaka, Hitoshi |
author_sort | Ishida, Takako |
collection | PubMed |
description | RAD51, an essential eukaryotic DNA recombinase, promotes homologous pairing and strand exchange during homologous recombination and the recombinational repair of double strand breaks. Mutations that up- or down-regulate RAD51 gene expression have been identified in several tumors, suggesting that inappropriate expression of the RAD51 activity may cause tumorigenesis. To identify chemical compounds that affect the RAD51 activity, in the present study, we performed the RAD51-mediated strand exchange assay in the presence of 185 chemical compounds. We found that 4,4′-diisothiocyanostilbene-2,2′-disulfonic acid (DIDS) efficiently inhibited the RAD51-mediated strand exchange. DIDS also inhibited the RAD51-mediated homologous pairing in the absence of RPA. A surface plasmon resonance analysis revealed that DIDS directly binds to RAD51. A gel mobility shift assay showed that DIDS significantly inhibited the DNA-binding activity of RAD51. Therefore, DIDS may bind near the DNA binding site(s) of RAD51 and compete with DNA for RAD51 binding. |
format | Text |
id | pubmed-2691838 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2009 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-26918382009-07-17 DIDS, a chemical compound that inhibits RAD51-mediated homologous pairing and strand exchange Ishida, Takako Takizawa, Yoshimasa Kainuma, Takashi Inoue, Jin Mikawa, Tsutomu Shibata, Takehiko Suzuki, Hidekazu Tashiro, Satoshi Kurumizaka, Hitoshi Nucleic Acids Res Genome Integrity, Repair and Replication RAD51, an essential eukaryotic DNA recombinase, promotes homologous pairing and strand exchange during homologous recombination and the recombinational repair of double strand breaks. Mutations that up- or down-regulate RAD51 gene expression have been identified in several tumors, suggesting that inappropriate expression of the RAD51 activity may cause tumorigenesis. To identify chemical compounds that affect the RAD51 activity, in the present study, we performed the RAD51-mediated strand exchange assay in the presence of 185 chemical compounds. We found that 4,4′-diisothiocyanostilbene-2,2′-disulfonic acid (DIDS) efficiently inhibited the RAD51-mediated strand exchange. DIDS also inhibited the RAD51-mediated homologous pairing in the absence of RPA. A surface plasmon resonance analysis revealed that DIDS directly binds to RAD51. A gel mobility shift assay showed that DIDS significantly inhibited the DNA-binding activity of RAD51. Therefore, DIDS may bind near the DNA binding site(s) of RAD51 and compete with DNA for RAD51 binding. Oxford University Press 2009-06 2009-03-30 /pmc/articles/PMC2691838/ /pubmed/19336413 http://dx.doi.org/10.1093/nar/gkp200 Text en © 2009 http://creativecommons.org/licenses/by-nc/2.0/uk/ The Author(s) This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/2.0/uk/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Genome Integrity, Repair and Replication Ishida, Takako Takizawa, Yoshimasa Kainuma, Takashi Inoue, Jin Mikawa, Tsutomu Shibata, Takehiko Suzuki, Hidekazu Tashiro, Satoshi Kurumizaka, Hitoshi DIDS, a chemical compound that inhibits RAD51-mediated homologous pairing and strand exchange |
title | DIDS, a chemical compound that inhibits RAD51-mediated homologous pairing and strand exchange |
title_full | DIDS, a chemical compound that inhibits RAD51-mediated homologous pairing and strand exchange |
title_fullStr | DIDS, a chemical compound that inhibits RAD51-mediated homologous pairing and strand exchange |
title_full_unstemmed | DIDS, a chemical compound that inhibits RAD51-mediated homologous pairing and strand exchange |
title_short | DIDS, a chemical compound that inhibits RAD51-mediated homologous pairing and strand exchange |
title_sort | dids, a chemical compound that inhibits rad51-mediated homologous pairing and strand exchange |
topic | Genome Integrity, Repair and Replication |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2691838/ https://www.ncbi.nlm.nih.gov/pubmed/19336413 http://dx.doi.org/10.1093/nar/gkp200 |
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