miRNA-dependent translational repression in the Drosophila ovary.

The Drosophila ovary is a tissue rich in post-transcriptional regulation of gene expression. Many of the regulatory factors are proteins identified via genetic screens. The more recent discovery of microRNAs, which in other animals and tissues appear to regulate translation of a large fraction of al...

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Main Authors: John Reich, Mark J Snee, Paul M Macdonald
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2009-01-01
Series:PLoS ONE
Online Access:http://europepmc.org/articles/PMC2645501?pdf=render
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spelling doaj-0b92720c38b94d6db62c38fbbf275b4b2020-11-25T01:51:13ZengPublic Library of Science (PLoS)PLoS ONE1932-62032009-01-0143e466910.1371/journal.pone.0004669miRNA-dependent translational repression in the Drosophila ovary.John ReichMark J SneePaul M MacdonaldThe Drosophila ovary is a tissue rich in post-transcriptional regulation of gene expression. Many of the regulatory factors are proteins identified via genetic screens. The more recent discovery of microRNAs, which in other animals and tissues appear to regulate translation of a large fraction of all mRNAs, raised the possibility that they too might act during oogenesis. However, there has been no direct demonstration of microRNA-dependent translational repression in the ovary.Here, quantitative analyses of transcript and protein levels of transgenes with or without synthetic miR-312 binding sites show that the binding sites do confer translational repression. This effect is dependent on the ability of the cells to produce microRNAs. By comparison with microRNA-dependent translational repression in other cell types, the regulated mRNAs and the protein factors that mediate repression were expected to be enriched in sponge bodies, subcellular structures with extensive similarities to the P bodies found in other cells. However, no such enrichment was observed.Our results reveal the variety of post-transcriptional regulatory mechanisms that operate in the Drosophila ovary, and have implications for the mechanisms of miRNA-dependent translational control used in the ovary.http://europepmc.org/articles/PMC2645501?pdf=render
collection DOAJ
language English
format Article
sources DOAJ
author John Reich
Mark J Snee
Paul M Macdonald
spellingShingle John Reich
Mark J Snee
Paul M Macdonald
miRNA-dependent translational repression in the Drosophila ovary.
PLoS ONE
author_facet John Reich
Mark J Snee
Paul M Macdonald
author_sort John Reich
title miRNA-dependent translational repression in the Drosophila ovary.
title_short miRNA-dependent translational repression in the Drosophila ovary.
title_full miRNA-dependent translational repression in the Drosophila ovary.
title_fullStr miRNA-dependent translational repression in the Drosophila ovary.
title_full_unstemmed miRNA-dependent translational repression in the Drosophila ovary.
title_sort mirna-dependent translational repression in the drosophila ovary.
publisher Public Library of Science (PLoS)
series PLoS ONE
issn 1932-6203
publishDate 2009-01-01
description The Drosophila ovary is a tissue rich in post-transcriptional regulation of gene expression. Many of the regulatory factors are proteins identified via genetic screens. The more recent discovery of microRNAs, which in other animals and tissues appear to regulate translation of a large fraction of all mRNAs, raised the possibility that they too might act during oogenesis. However, there has been no direct demonstration of microRNA-dependent translational repression in the ovary.Here, quantitative analyses of transcript and protein levels of transgenes with or without synthetic miR-312 binding sites show that the binding sites do confer translational repression. This effect is dependent on the ability of the cells to produce microRNAs. By comparison with microRNA-dependent translational repression in other cell types, the regulated mRNAs and the protein factors that mediate repression were expected to be enriched in sponge bodies, subcellular structures with extensive similarities to the P bodies found in other cells. However, no such enrichment was observed.Our results reveal the variety of post-transcriptional regulatory mechanisms that operate in the Drosophila ovary, and have implications for the mechanisms of miRNA-dependent translational control used in the ovary.
url http://europepmc.org/articles/PMC2645501?pdf=render
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