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Dicer-independent processing of small RNA duplexes: mechanistic insights and applications

MicroRNAs (miRNAs) play a pivotal role in the regulation of cellular gene expression via the conserved RNA interference (RNAi) mechanism. Biogenesis of the unusual miR-451 does not require Dicer. This molecule is instead processed by the Argonaute 2 (Ago2) enzyme. Similarly, unconventional short hai...

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Detalles Bibliográficos
Autores principales: Herrera-Carrillo, Elena, Berkhout, Ben
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5737282/
https://www.ncbi.nlm.nih.gov/pubmed/28977573
http://dx.doi.org/10.1093/nar/gkx779
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author Herrera-Carrillo, Elena
Berkhout, Ben
author_facet Herrera-Carrillo, Elena
Berkhout, Ben
author_sort Herrera-Carrillo, Elena
collection PubMed
description MicroRNAs (miRNAs) play a pivotal role in the regulation of cellular gene expression via the conserved RNA interference (RNAi) mechanism. Biogenesis of the unusual miR-451 does not require Dicer. This molecule is instead processed by the Argonaute 2 (Ago2) enzyme. Similarly, unconventional short hairpin RNA (shRNA) molecules have been designed as miR-451 mimics that rely exclusively on Ago2 for maturation. We will review recent progress made in the understanding of this alternative processing route. Next, we describe different Dicer-independent shRNA designs that have been developed and discuss their therapeutic advantages and disadvantages. As an example, we will present the route towards development of a durable gene therapy against HIV-1.
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spelling pubmed-57372822018-01-08 Dicer-independent processing of small RNA duplexes: mechanistic insights and applications Herrera-Carrillo, Elena Berkhout, Ben Nucleic Acids Res Survey and Summary MicroRNAs (miRNAs) play a pivotal role in the regulation of cellular gene expression via the conserved RNA interference (RNAi) mechanism. Biogenesis of the unusual miR-451 does not require Dicer. This molecule is instead processed by the Argonaute 2 (Ago2) enzyme. Similarly, unconventional short hairpin RNA (shRNA) molecules have been designed as miR-451 mimics that rely exclusively on Ago2 for maturation. We will review recent progress made in the understanding of this alternative processing route. Next, we describe different Dicer-independent shRNA designs that have been developed and discuss their therapeutic advantages and disadvantages. As an example, we will present the route towards development of a durable gene therapy against HIV-1. Oxford University Press 2017-10-13 2017-08-31 /pmc/articles/PMC5737282/ /pubmed/28977573 http://dx.doi.org/10.1093/nar/gkx779 Text en © The Author(s) 2017. Published by Oxford University Press on behalf of Nucleic Acids Research. http://creativecommons.org/licenses/by-nc/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by-nc/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com
spellingShingle Survey and Summary
Herrera-Carrillo, Elena
Berkhout, Ben
Dicer-independent processing of small RNA duplexes: mechanistic insights and applications
title Dicer-independent processing of small RNA duplexes: mechanistic insights and applications
title_full Dicer-independent processing of small RNA duplexes: mechanistic insights and applications
title_fullStr Dicer-independent processing of small RNA duplexes: mechanistic insights and applications
title_full_unstemmed Dicer-independent processing of small RNA duplexes: mechanistic insights and applications
title_short Dicer-independent processing of small RNA duplexes: mechanistic insights and applications
title_sort dicer-independent processing of small rna duplexes: mechanistic insights and applications
topic Survey and Summary
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5737282/
https://www.ncbi.nlm.nih.gov/pubmed/28977573
http://dx.doi.org/10.1093/nar/gkx779
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