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Host Double Strand Break Repair Generates HIV-1 Strains Resistant to CRISPR/Cas9

CRISPR/Cas9 genome editing has been proposed as a therapeutic treatment for HIV-1 infection. CRISPR/Cas9 induced double strand breaks (DSBs) targeted to the integrated viral genome have been shown to decrease production of progeny virus. Unfortunately HIV-1 evolves rapidly and may readily produce CR...

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Détails bibliographiques
Publié dans:Sci Rep
Auteurs principaux: Yoder, Kristine E., Bundschuh, Ralf
Format: Artigo
Langue:Inglês
Publié: Nature Publishing Group 2016
Sujets:
Accès en ligne:https://ncbi.nlm.nih.gov/pmc/articles/PMC4941621/
https://ncbi.nlm.nih.gov/pubmed/27404981
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/srep29530
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