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Evolution of Nova-Dependent Splicing Regulation in the Brain

A large number of alternative exons are spliced with tissue-specific patterns, but little is known about how such patterns have evolved. Here, we study the conservation of the neuron-specific splicing factors Nova1 and Nova2 and of the alternatively spliced exons they regulate in mouse brain. Wherea...

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Autores principales: Jelen, Nejc, Ule, Jernej, Živin, Marko, Darnell, Robert B
Formato: Texto
Lenguaje:English
Publicado: Public Library of Science 2007
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2014790/
https://www.ncbi.nlm.nih.gov/pubmed/17937501
http://dx.doi.org/10.1371/journal.pgen.0030173
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author Jelen, Nejc
Ule, Jernej
Živin, Marko
Darnell, Robert B
author_facet Jelen, Nejc
Ule, Jernej
Živin, Marko
Darnell, Robert B
author_sort Jelen, Nejc
collection PubMed
description A large number of alternative exons are spliced with tissue-specific patterns, but little is known about how such patterns have evolved. Here, we study the conservation of the neuron-specific splicing factors Nova1 and Nova2 and of the alternatively spliced exons they regulate in mouse brain. Whereas Nova RNA binding domains are 94% identical across vertebrate species, Nova-dependent splicing silencer and enhancer elements (YCAY clusters) show much greater divergence, as less than 50% of mouse YCAY clusters are conserved at orthologous positions in the zebrafish genome. To study the relation between the evolution of tissue-specific splicing and YCAY clusters, we compared the brain-specific splicing of Nova-regulated exons in zebrafish, chicken, and mouse. The presence of YCAY clusters in lower vertebrates invariably predicted conservation of brain-specific splicing across species, whereas their absence in lower vertebrates correlated with a loss of alternative splicing. We hypothesize that evolution of Nova-regulated splicing in higher vertebrates proceeds mainly through changes in cis-acting elements, that tissue-specific splicing might in some cases evolve in a single step corresponding to evolution of a YCAY cluster, and that the conservation level of YCAY clusters relates to the functions encoded by the regulated RNAs.
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spelling pubmed-20147902007-10-25 Evolution of Nova-Dependent Splicing Regulation in the Brain Jelen, Nejc Ule, Jernej Živin, Marko Darnell, Robert B PLoS Genet Research Article A large number of alternative exons are spliced with tissue-specific patterns, but little is known about how such patterns have evolved. Here, we study the conservation of the neuron-specific splicing factors Nova1 and Nova2 and of the alternatively spliced exons they regulate in mouse brain. Whereas Nova RNA binding domains are 94% identical across vertebrate species, Nova-dependent splicing silencer and enhancer elements (YCAY clusters) show much greater divergence, as less than 50% of mouse YCAY clusters are conserved at orthologous positions in the zebrafish genome. To study the relation between the evolution of tissue-specific splicing and YCAY clusters, we compared the brain-specific splicing of Nova-regulated exons in zebrafish, chicken, and mouse. The presence of YCAY clusters in lower vertebrates invariably predicted conservation of brain-specific splicing across species, whereas their absence in lower vertebrates correlated with a loss of alternative splicing. We hypothesize that evolution of Nova-regulated splicing in higher vertebrates proceeds mainly through changes in cis-acting elements, that tissue-specific splicing might in some cases evolve in a single step corresponding to evolution of a YCAY cluster, and that the conservation level of YCAY clusters relates to the functions encoded by the regulated RNAs. Public Library of Science 2007-10 2007-10-12 /pmc/articles/PMC2014790/ /pubmed/17937501 http://dx.doi.org/10.1371/journal.pgen.0030173 Text en © 2007 Jelen et al. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Jelen, Nejc
Ule, Jernej
Živin, Marko
Darnell, Robert B
Evolution of Nova-Dependent Splicing Regulation in the Brain
title Evolution of Nova-Dependent Splicing Regulation in the Brain
title_full Evolution of Nova-Dependent Splicing Regulation in the Brain
title_fullStr Evolution of Nova-Dependent Splicing Regulation in the Brain
title_full_unstemmed Evolution of Nova-Dependent Splicing Regulation in the Brain
title_short Evolution of Nova-Dependent Splicing Regulation in the Brain
title_sort evolution of nova-dependent splicing regulation in the brain
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2014790/
https://www.ncbi.nlm.nih.gov/pubmed/17937501
http://dx.doi.org/10.1371/journal.pgen.0030173
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