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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...
Enregistré dans:
| Publié dans: | Nat Commun |
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| Auteurs principaux: | , , , , |
| Format: | Artigo |
| Langue: | Inglês |
| Publié: |
Nature Pub. Group
2015
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| Sujets: | |
| Accès en ligne: | 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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