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The RNA helicase MOV10L1 binds piRNA precursors to initiate piRNA processing

Piwi–piRNA (Piwi-interacting RNA) ribonucleoproteins (piRNPs) enforce retrotransposon silencing, a function critical for preserving the genome integrity of germ cells. The molecular functions of most of the factors that have been genetically implicated in primary piRNA biogenesis are still elusive....

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Autores principales: Vourekas, Anastassios, Zheng, Ke, Fu, Qi, Maragkakis, Manolis, Alexiou, Panagiotis, Ma, Jing, Pillai, Ramesh S., Mourelatos, Zissimos, Wang, P. Jeremy
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cold Spring Harbor Laboratory Press 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4378194/
https://www.ncbi.nlm.nih.gov/pubmed/25762440
http://dx.doi.org/10.1101/gad.254631.114
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author Vourekas, Anastassios
Zheng, Ke
Fu, Qi
Maragkakis, Manolis
Alexiou, Panagiotis
Ma, Jing
Pillai, Ramesh S.
Mourelatos, Zissimos
Wang, P. Jeremy
author_facet Vourekas, Anastassios
Zheng, Ke
Fu, Qi
Maragkakis, Manolis
Alexiou, Panagiotis
Ma, Jing
Pillai, Ramesh S.
Mourelatos, Zissimos
Wang, P. Jeremy
author_sort Vourekas, Anastassios
collection PubMed
description Piwi–piRNA (Piwi-interacting RNA) ribonucleoproteins (piRNPs) enforce retrotransposon silencing, a function critical for preserving the genome integrity of germ cells. The molecular functions of most of the factors that have been genetically implicated in primary piRNA biogenesis are still elusive. Here we show that MOV10L1 exhibits 5′-to-3′ directional RNA-unwinding activity in vitro and that a point mutation that abolishes this activity causes a failure in primary piRNA biogenesis in vivo. We demonstrate that MOV10L1 selectively binds piRNA precursor transcripts and is essential for the generation of intermediate piRNA processing fragments that are subsequently loaded to Piwi proteins. Multiple analyses suggest an intimate coupling of piRNA precursor processing with elements of local secondary structures such as G quadruplexes. Our results support a model in which MOV10L1 RNA helicase activity promotes unwinding and funneling of the single-stranded piRNA precursor transcripts to the endonuclease that catalyzes the first cleavage step of piRNA processing.
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spelling pubmed-43781942015-09-15 The RNA helicase MOV10L1 binds piRNA precursors to initiate piRNA processing Vourekas, Anastassios Zheng, Ke Fu, Qi Maragkakis, Manolis Alexiou, Panagiotis Ma, Jing Pillai, Ramesh S. Mourelatos, Zissimos Wang, P. Jeremy Genes Dev Research Papers Piwi–piRNA (Piwi-interacting RNA) ribonucleoproteins (piRNPs) enforce retrotransposon silencing, a function critical for preserving the genome integrity of germ cells. The molecular functions of most of the factors that have been genetically implicated in primary piRNA biogenesis are still elusive. Here we show that MOV10L1 exhibits 5′-to-3′ directional RNA-unwinding activity in vitro and that a point mutation that abolishes this activity causes a failure in primary piRNA biogenesis in vivo. We demonstrate that MOV10L1 selectively binds piRNA precursor transcripts and is essential for the generation of intermediate piRNA processing fragments that are subsequently loaded to Piwi proteins. Multiple analyses suggest an intimate coupling of piRNA precursor processing with elements of local secondary structures such as G quadruplexes. Our results support a model in which MOV10L1 RNA helicase activity promotes unwinding and funneling of the single-stranded piRNA precursor transcripts to the endonuclease that catalyzes the first cleavage step of piRNA processing. Cold Spring Harbor Laboratory Press 2015-03-15 /pmc/articles/PMC4378194/ /pubmed/25762440 http://dx.doi.org/10.1101/gad.254631.114 Text en © 2015 Vourekas et al.; Published by Cold Spring Harbor Laboratory Press http://creativecommons.org/licenses/by-nc/4.0/ This article is distributed exclusively by Cold Spring Harbor Laboratory Press for the first six months after the full-issue publication date (see http://genesdev.cshlp.org/site/misc/terms.xhtml). After six months, it is available under a Creative Commons License (Attribution-NonCommercial 4.0 International), as described at http://creativecommons.org/licenses/by-nc/4.0/.
spellingShingle Research Papers
Vourekas, Anastassios
Zheng, Ke
Fu, Qi
Maragkakis, Manolis
Alexiou, Panagiotis
Ma, Jing
Pillai, Ramesh S.
Mourelatos, Zissimos
Wang, P. Jeremy
The RNA helicase MOV10L1 binds piRNA precursors to initiate piRNA processing
title The RNA helicase MOV10L1 binds piRNA precursors to initiate piRNA processing
title_full The RNA helicase MOV10L1 binds piRNA precursors to initiate piRNA processing
title_fullStr The RNA helicase MOV10L1 binds piRNA precursors to initiate piRNA processing
title_full_unstemmed The RNA helicase MOV10L1 binds piRNA precursors to initiate piRNA processing
title_short The RNA helicase MOV10L1 binds piRNA precursors to initiate piRNA processing
title_sort rna helicase mov10l1 binds pirna precursors to initiate pirna processing
topic Research Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4378194/
https://www.ncbi.nlm.nih.gov/pubmed/25762440
http://dx.doi.org/10.1101/gad.254631.114
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