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Argonaute-3 activates the let-7a passenger strand microRNA

MicroRNA duplices are separated into a guide and a passenger strand. By convention, the guide represents the active microRNA while the passenger is supposedly degraded. However, passenger strands also emerge as active microRNAs. It is unknown whether the guide-to-passenger-strand ratio can be active...

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Detalles Bibliográficos
Autores principales: Winter, Julia, Diederichs, Sven
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Landes Bioscience 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3866245/
https://www.ncbi.nlm.nih.gov/pubmed/24100239
http://dx.doi.org/10.4161/rna.26424
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author Winter, Julia
Diederichs, Sven
author_facet Winter, Julia
Diederichs, Sven
author_sort Winter, Julia
collection PubMed
description MicroRNA duplices are separated into a guide and a passenger strand. By convention, the guide represents the active microRNA while the passenger is supposedly degraded. However, passenger strands also emerge as active microRNAs. It is unknown whether the guide-to-passenger-strand ratio can be actively regulated and which factors influence strand incorporation into the RISC. Here, we identify a microRNA with a variable guide-to-passenger-strand ratio along with its regulatory factor: Human Argonaute-3 specifically enhances the passenger strand expression and activity of the tumor suppressor microRNA let-7a. This post-maturational effect is mediated by the Ago3 PAZ and MID domains yielding an elevated affinity for let-7a-3p. Notably, this is independent of the 5′-terminal basepair stability, challenging the universality of the respective rule for microRNA strand selection. Thus, this study uncovers the first protein regulator of the ratio between microRNA guide and passenger strand expression and activity.
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spelling pubmed-38662452013-12-30 Argonaute-3 activates the let-7a passenger strand microRNA Winter, Julia Diederichs, Sven RNA Biol Research Paper MicroRNA duplices are separated into a guide and a passenger strand. By convention, the guide represents the active microRNA while the passenger is supposedly degraded. However, passenger strands also emerge as active microRNAs. It is unknown whether the guide-to-passenger-strand ratio can be actively regulated and which factors influence strand incorporation into the RISC. Here, we identify a microRNA with a variable guide-to-passenger-strand ratio along with its regulatory factor: Human Argonaute-3 specifically enhances the passenger strand expression and activity of the tumor suppressor microRNA let-7a. This post-maturational effect is mediated by the Ago3 PAZ and MID domains yielding an elevated affinity for let-7a-3p. Notably, this is independent of the 5′-terminal basepair stability, challenging the universality of the respective rule for microRNA strand selection. Thus, this study uncovers the first protein regulator of the ratio between microRNA guide and passenger strand expression and activity. Landes Bioscience 2013-10-01 2013-10-02 /pmc/articles/PMC3866245/ /pubmed/24100239 http://dx.doi.org/10.4161/rna.26424 Text en Copyright © 2013 Landes Bioscience http://creativecommons.org/licenses/by-nc/3.0/ This is an open-access article licensed under a Creative Commons Attribution-NonCommercial 3.0 Unported License. The article may be redistributed, reproduced, and reused for non-commercial purposes, provided the original source is properly cited.
spellingShingle Research Paper
Winter, Julia
Diederichs, Sven
Argonaute-3 activates the let-7a passenger strand microRNA
title Argonaute-3 activates the let-7a passenger strand microRNA
title_full Argonaute-3 activates the let-7a passenger strand microRNA
title_fullStr Argonaute-3 activates the let-7a passenger strand microRNA
title_full_unstemmed Argonaute-3 activates the let-7a passenger strand microRNA
title_short Argonaute-3 activates the let-7a passenger strand microRNA
title_sort argonaute-3 activates the let-7a passenger strand microrna
topic Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3866245/
https://www.ncbi.nlm.nih.gov/pubmed/24100239
http://dx.doi.org/10.4161/rna.26424
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