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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....
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Cold Spring Harbor Laboratory Press
2015
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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. |
format | Online Article Text |
id | pubmed-4378194 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Cold Spring Harbor Laboratory Press |
record_format | MEDLINE/PubMed |
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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