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The DNA structure and sequence preferences of WRN underlie its function in telomeric recombination events

Telomeric abnormalities caused by loss of function of the RecQ helicase WRN are linked to the multiple premature ageing phenotypes that characterize Werner syndrome. Here we examine WRN's role in telomeric maintenance, by comparing its action on a variety of DNA structures without or with telom...

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Publicado en:Nat Commun
Main Authors: Edwards, Deanna N., Machwe, Amrita, Chen, Li, Bohr, Vilhelm A., Orren, David K.
Formato: Artigo
Idioma:Inglês
Publicado: Nature Pub. Group 2015
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Acceso en liña:https://ncbi.nlm.nih.gov/pmc/articles/PMC4589872/
https://ncbi.nlm.nih.gov/pubmed/26420422
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/ncomms9331
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