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Non-B DNA-forming Sequences and WRN Deficiency Independently Increase the Frequency of Base Substitution in Human Cells

Although alternative DNA secondary structures (non-B DNA) can induce genomic rearrangements, their associated mutational spectra remain largely unknown. The helicase activity of WRN, which is absent in the human progeroid Werner syndrome, is thought to counteract this genomic instability. We determi...

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書誌詳細
主要な著者: Bacolla, Albino, Wang, Guliang, Jain, Aklank, Chuzhanova, Nadia A., Cer, Regina Z., Collins, Jack R., Cooper, David N., Bohr, Vilhelm A., Vasquez, Karen M.
フォーマット: Artigo
言語:Inglês
出版事項: American Society for Biochemistry and Molecular Biology 2011
主題:
オンライン・アクセス:https://ncbi.nlm.nih.gov/pmc/articles/PMC3060453/
https://ncbi.nlm.nih.gov/pubmed/21285356
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1074/jbc.M110.176636
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