| Literature DB >> 31843447 |
Jun Xie1, Phillip W L Tai2, Alexander Brown2, Shoufang Gong2, Sha Zhu2, Yi Wang3, Chengjian Li4, Cansu Colpan5, Qin Su6, Ran He6, Hong Ma6, Jia Li2, Hanqing Ye2, Jihye Ko6, Phillip D Zamore7, Guangping Gao8.
Abstract
Short hairpin RNAs that are delivered by recombinant adeno-associated virus (rAAV) have the potential to elicit long-term RNAi therapy for human disease. However, the discovery that short hairpin sequences can cause truncation of the rAAV genome calls into question the efficiency and gene-silencing specificity of this strategy in humans. Here, we report that embedding the guide strand of a small silencing RNA into an artificial microRNA (miRNA) scaffold derived from mouse miRNA-33 ensures rAAV genomic integrity and reduces off-targeting by 10-fold, while maintaining effective in vivo target gene repression in mice. Published by Elsevier Inc.Entities:
Mesh:
Substances:
Year: 2019 PMID: 31843447 PMCID: PMC7001000 DOI: 10.1016/j.ymthe.2019.11.018
Source DB: PubMed Journal: Mol Ther ISSN: 1525-0016 Impact factor: 11.454