The Drosophila Helicase MLE Targets Hairpin Structures in Genomic Transcripts.

RNA hairpins are a common type of secondary structures that play a role in every aspect of RNA biochemistry including RNA editing, mRNA stability, localization and translation of transcripts, and in the activation of the RNA interference (RNAi) and microRNA (miRNA) pathways. Participation in these f...

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Main Authors: Simona Cugusi, Yujing Li, Peng Jin, John C Lucchesi
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2016-01-01
Series:PLoS Genetics
Online Access:http://europepmc.org/articles/PMC4710571?pdf=render
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spelling doaj-509513a048764ea3b096d154650c78bf2020-11-25T02:30:16ZengPublic Library of Science (PLoS)PLoS Genetics1553-73901553-74042016-01-01121e100576110.1371/journal.pgen.1005761The Drosophila Helicase MLE Targets Hairpin Structures in Genomic Transcripts.Simona CugusiYujing LiPeng JinJohn C LucchesiRNA hairpins are a common type of secondary structures that play a role in every aspect of RNA biochemistry including RNA editing, mRNA stability, localization and translation of transcripts, and in the activation of the RNA interference (RNAi) and microRNA (miRNA) pathways. Participation in these functions often requires restructuring the RNA molecules by the association of single-strand (ss) RNA-binding proteins or by the action of helicases. The Drosophila MLE helicase has long been identified as a member of the MSL complex responsible for dosage compensation. The complex includes one of two long non-coding RNAs and MLE was shown to remodel the roX RNA hairpin structures in order to initiate assembly of the complex. Here we report that this function of MLE may apply to the hairpins present in the primary RNA transcripts that generate the small molecules responsible for RNA interference. Using stocks from the Transgenic RNAi Project and the Vienna Drosophila Research Center, we show that MLE specifically targets hairpin RNAs at their site of transcription. The association of MLE at these sites is independent of sequence and chromosome location. We use two functional assays to test the biological relevance of this association and determine that MLE participates in the RNAi pathway.http://europepmc.org/articles/PMC4710571?pdf=render
collection DOAJ
language English
format Article
sources DOAJ
author Simona Cugusi
Yujing Li
Peng Jin
John C Lucchesi
spellingShingle Simona Cugusi
Yujing Li
Peng Jin
John C Lucchesi
The Drosophila Helicase MLE Targets Hairpin Structures in Genomic Transcripts.
PLoS Genetics
author_facet Simona Cugusi
Yujing Li
Peng Jin
John C Lucchesi
author_sort Simona Cugusi
title The Drosophila Helicase MLE Targets Hairpin Structures in Genomic Transcripts.
title_short The Drosophila Helicase MLE Targets Hairpin Structures in Genomic Transcripts.
title_full The Drosophila Helicase MLE Targets Hairpin Structures in Genomic Transcripts.
title_fullStr The Drosophila Helicase MLE Targets Hairpin Structures in Genomic Transcripts.
title_full_unstemmed The Drosophila Helicase MLE Targets Hairpin Structures in Genomic Transcripts.
title_sort drosophila helicase mle targets hairpin structures in genomic transcripts.
publisher Public Library of Science (PLoS)
series PLoS Genetics
issn 1553-7390
1553-7404
publishDate 2016-01-01
description RNA hairpins are a common type of secondary structures that play a role in every aspect of RNA biochemistry including RNA editing, mRNA stability, localization and translation of transcripts, and in the activation of the RNA interference (RNAi) and microRNA (miRNA) pathways. Participation in these functions often requires restructuring the RNA molecules by the association of single-strand (ss) RNA-binding proteins or by the action of helicases. The Drosophila MLE helicase has long been identified as a member of the MSL complex responsible for dosage compensation. The complex includes one of two long non-coding RNAs and MLE was shown to remodel the roX RNA hairpin structures in order to initiate assembly of the complex. Here we report that this function of MLE may apply to the hairpins present in the primary RNA transcripts that generate the small molecules responsible for RNA interference. Using stocks from the Transgenic RNAi Project and the Vienna Drosophila Research Center, we show that MLE specifically targets hairpin RNAs at their site of transcription. The association of MLE at these sites is independent of sequence and chromosome location. We use two functional assays to test the biological relevance of this association and determine that MLE participates in the RNAi pathway.
url http://europepmc.org/articles/PMC4710571?pdf=render
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