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Regulation of gene expression through inefficient splicing of U12-type introns

U12-type introns are a rare class of nuclear introns that are removed by a dedicated U12-dependent spliceosome and are thought to regulate the expression of their target genes owing through their slower splicing reaction. Recent genome-wide studies on the splicing of U12-type introns are now providi...

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Autores principales: Niemelä, Elina H, Frilander, Mikko J
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Taylor & Francis 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4615840/
https://www.ncbi.nlm.nih.gov/pubmed/25692230
http://dx.doi.org/10.1080/15476286.2014.996454
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author Niemelä, Elina H
Frilander, Mikko J
author_facet Niemelä, Elina H
Frilander, Mikko J
author_sort Niemelä, Elina H
collection PubMed
description U12-type introns are a rare class of nuclear introns that are removed by a dedicated U12-dependent spliceosome and are thought to regulate the expression of their target genes owing through their slower splicing reaction. Recent genome-wide studies on the splicing of U12-type introns are now providing new insights on the biological significance of this parallel splicing machinery. The new studies cover multiple different organisms and experimental systems, including human patient cells with mutations in the components of the minor spliceosome, zebrafish with similar mutations and various experimentally manipulated human cells and Arabidopsis plants. Here, we will discuss the potential implications of these studies on the understanding of the mechanism and regulation of the minor spliceosome, as well as their medical implications.
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spelling pubmed-46158402016-02-03 Regulation of gene expression through inefficient splicing of U12-type introns Niemelä, Elina H Frilander, Mikko J RNA Biol Points-of-View U12-type introns are a rare class of nuclear introns that are removed by a dedicated U12-dependent spliceosome and are thought to regulate the expression of their target genes owing through their slower splicing reaction. Recent genome-wide studies on the splicing of U12-type introns are now providing new insights on the biological significance of this parallel splicing machinery. The new studies cover multiple different organisms and experimental systems, including human patient cells with mutations in the components of the minor spliceosome, zebrafish with similar mutations and various experimentally manipulated human cells and Arabidopsis plants. Here, we will discuss the potential implications of these studies on the understanding of the mechanism and regulation of the minor spliceosome, as well as their medical implications. Taylor & Francis 2015-02-18 /pmc/articles/PMC4615840/ /pubmed/25692230 http://dx.doi.org/10.1080/15476286.2014.996454 Text en © 2014 The Author(s). Published with license by Taylor & Francis Group, LLC http://creativecommons.org/licenses/by-nc/3.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution-Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0/), which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. The moral rights of the named author(s) have been asserted.
spellingShingle Points-of-View
Niemelä, Elina H
Frilander, Mikko J
Regulation of gene expression through inefficient splicing of U12-type introns
title Regulation of gene expression through inefficient splicing of U12-type introns
title_full Regulation of gene expression through inefficient splicing of U12-type introns
title_fullStr Regulation of gene expression through inefficient splicing of U12-type introns
title_full_unstemmed Regulation of gene expression through inefficient splicing of U12-type introns
title_short Regulation of gene expression through inefficient splicing of U12-type introns
title_sort regulation of gene expression through inefficient splicing of u12-type introns
topic Points-of-View
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4615840/
https://www.ncbi.nlm.nih.gov/pubmed/25692230
http://dx.doi.org/10.1080/15476286.2014.996454
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