The breast cancer tumor suppressor BRCA2 promotes the specific targeting of RAD51 to single-stranded DNA View Full Text


Ontology type: schema:ScholarlyArticle      Open Access: True


Article Info

DATE

2010-10

AUTHORS

Tina Thorslund, Michael J McIlwraith, Sarah A Compton, Sergey Lekomtsev, Mark Petronczki, Jack D Griffith, Stephen C West

ABSTRACT

Individuals with BRCA2 mutations are predisposed to breast cancers owing to genome instability. To determine the functions of BRCA2, the human protein was purified. It was found to bind selectively to single-stranded DNA (ssDNA), and to ssDNA in tailed duplexes and replication fork structures. Monomeric and dimeric forms of BRCA2 were observed by EM. BRCA2 directed the binding of RAD51 recombinase to ssDNA, reduced the binding of RAD51 to duplex DNA and stimulated RAD51-mediated DNA strand exchange. These observations provide a molecular basis for the role of BRCA2 in the maintenance of genome stability. More... »

PAGES

1263

Identifiers

URI

http://scigraph.springernature.com/pub.10.1038/nsmb.1905

DOI

http://dx.doi.org/10.1038/nsmb.1905

DIMENSIONS

https://app.dimensions.ai/details/publication/pub.1027318611

PUBMED

https://www.ncbi.nlm.nih.gov/pubmed/20729858


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