©The Author(s) 2016. Published by Baishideng Publishing Group Inc. All rights reserved.
World J Exp Med. May 20, 2016; 6(2): 37-54
Published online May 20, 2016. doi: 10.5493/wjem.v6.i2.37
Published online May 20, 2016. doi: 10.5493/wjem.v6.i2.37
MicroRNA-regulated viral vectors for gene therapy
Anja Geisler, Henry Fechner, Department of Applied Biochemistry, Institute of Biotechnology, Technische Universität Berlin, 13355 Berlin, Germany
Author contributions: The authors equally contributed to this paper with conception and design of the study, literature review and analysis, drafting and critical revision and editing, and final approval of the final version.
Supported by The Deutsche Forschungsgemeinschaft, Nos. FE785/2-2 and FE785/4-1; and the Bundesministerium für Bildung und Entwicklung, No. 031A331.
Conflict-of-interest statement: The authors declare no conflict of interest.
Correspondence to: Henry Fechner, DVM, Department of Applied Biochemistry, Institute of Biotechnology, Technische Universität Berlin, Gustav-Meyer-Allee 25, 13355 Berlin, Germany. henry.fechner@tu-berlin.de
Telephone: +49-30-31472181 Fax: +49-30-31427502
Received: August 27, 2015
Peer-review started: August 31, 2015
First decision: October 27, 2015
Revised: March 2, 2016
Accepted: March 17, 2016
Article in press: March 18, 2016
Published online: May 20, 2016
Processing time: 263 Days and 14.5 Hours
Peer-review started: August 31, 2015
First decision: October 27, 2015
Revised: March 2, 2016
Accepted: March 17, 2016
Article in press: March 18, 2016
Published online: May 20, 2016
Processing time: 263 Days and 14.5 Hours
Core Tip
Core tip: Post-transcriptional microRNA-induced suppression of gene expression is a simple new, highly efficient technology to restrict transgene expression to a specific tissue. It is based on the insertion of a target sequence for a cell-specifically expressed microRNA, typically into the 3’ untranslated region of a transgene expression cassette. MicroRNA-induced regulation can result in an up to 100-fold reduction of transgene expression in tissues where expression is not desired. This targeting strategy can be used in combination with other targeting strategies to further improve vector specificity for gene therapeutic approaches.