| Literature DB >> 27357627 |
Xiaoou Jiang1, Han Yu1, Cui Rong Teo1, Genim Siu Xian Tan1, Sok Chin Goh1, Parasvi Patel1,2, Yiqiang Kevin Chua1, Nasirah Banu Sahul Hameed3, Antonio Bertoletti3, Volker Patzel1.
Abstract
Dumbbell-shaped DNA minimal vectors lacking nontherapeutic genes and bacterial sequences are considered a stable, safe alternative to viral, nonviral, and naked plasmid-based gene-transfer systems. We investigated novel molecular features of dumbbell vectors aiming to reduce vector size and to improve the expression of noncoding or coding RNA. We minimized small hairpin RNA (shRNA) or microRNA (miRNA) expressing dumbbell vectors in size down to 130 bp generating the smallest genetic expression vectors reported. This was achieved by using a minimal H1 promoter with integrated transcriptional terminator transcribing the RNA hairpin structure around the dumbbell loop. Such vectors were generated with high conversion yields using a novel protocol. Minimized shRNA-expressing dumbbells showed accelerated kinetics of delivery and transcription leading to enhanced gene silencing in human tissue culture cells. In primary human T cells, minimized miRNA-expressing dumbbells revealed higher stability and triggered stronger target gene suppression as compared with plasmids and miRNA mimics. Dumbbell-driven gene expression was enhanced up to 56- or 160-fold by implementation of an intron and the SV40 enhancer compared with control dumbbells or plasmids. Advanced dumbbell vectors may represent one option to close the gap between durable expression that is achievable with integrating viral vectors and short-term effects triggered by naked RNA.Entities:
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Year: 2016 PMID: 27357627 PMCID: PMC5113105 DOI: 10.1038/mt.2016.138
Source DB: PubMed Journal: Mol Ther ISSN: 1525-0016 Impact factor: 11.454