Cargando…

The low information content of Neurospora splicing signals: implications for RNA splicing and intron origin

When we expressed a small (0.9 kb) nonprotein-coding transcript derived from the mitochondrial VS plasmid in the nucleus of Neurospora we found that it was efficiently spliced at one or more of eight 5′ splice sites and ten 3′ splice sites, which are present apparently by chance in the sequence. Fur...

Descripción completa

Detalles Bibliográficos
Autores principales: Collins, Richard A., Stajich, Jason E., Field, Deborah J., Olive, Joan E., DeAbreu, Diane M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cold Spring Harbor Laboratory Press 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4408805/
https://www.ncbi.nlm.nih.gov/pubmed/25805857
http://dx.doi.org/10.1261/rna.047985.114
_version_ 1782368110458699776
author Collins, Richard A.
Stajich, Jason E.
Field, Deborah J.
Olive, Joan E.
DeAbreu, Diane M.
author_facet Collins, Richard A.
Stajich, Jason E.
Field, Deborah J.
Olive, Joan E.
DeAbreu, Diane M.
author_sort Collins, Richard A.
collection PubMed
description When we expressed a small (0.9 kb) nonprotein-coding transcript derived from the mitochondrial VS plasmid in the nucleus of Neurospora we found that it was efficiently spliced at one or more of eight 5′ splice sites and ten 3′ splice sites, which are present apparently by chance in the sequence. Further experimental and bioinformatic analyses of other mitochondrial plasmids, random sequences, and natural nuclear genes in Neurospora and other fungi indicate that fungal spliceosomes recognize a wide range of 5′ splice site and branchpoint sequences and predict introns to be present at high frequency in random sequence. In contrast, analysis of intronless fungal nuclear genes indicates that branchpoint, 5′ splice site and 3′ splice site consensus sequences are underrepresented compared with random sequences. This underrepresentation of splicing signals is sufficient to deplete the nuclear genome of splice sites at locations that do not comprise biologically relevant introns. Thus, the splicing machinery can recognize a wide range of splicing signal sequences, but splicing still occurs with great accuracy, not because the splicing machinery distinguishes correct from incorrect introns, but because incorrect introns are substantially depleted from the genome.
format Online
Article
Text
id pubmed-4408805
institution National Center for Biotechnology Information
language English
publishDate 2015
publisher Cold Spring Harbor Laboratory Press
record_format MEDLINE/PubMed
spelling pubmed-44088052016-05-01 The low information content of Neurospora splicing signals: implications for RNA splicing and intron origin Collins, Richard A. Stajich, Jason E. Field, Deborah J. Olive, Joan E. DeAbreu, Diane M. RNA Articles When we expressed a small (0.9 kb) nonprotein-coding transcript derived from the mitochondrial VS plasmid in the nucleus of Neurospora we found that it was efficiently spliced at one or more of eight 5′ splice sites and ten 3′ splice sites, which are present apparently by chance in the sequence. Further experimental and bioinformatic analyses of other mitochondrial plasmids, random sequences, and natural nuclear genes in Neurospora and other fungi indicate that fungal spliceosomes recognize a wide range of 5′ splice site and branchpoint sequences and predict introns to be present at high frequency in random sequence. In contrast, analysis of intronless fungal nuclear genes indicates that branchpoint, 5′ splice site and 3′ splice site consensus sequences are underrepresented compared with random sequences. This underrepresentation of splicing signals is sufficient to deplete the nuclear genome of splice sites at locations that do not comprise biologically relevant introns. Thus, the splicing machinery can recognize a wide range of splicing signal sequences, but splicing still occurs with great accuracy, not because the splicing machinery distinguishes correct from incorrect introns, but because incorrect introns are substantially depleted from the genome. Cold Spring Harbor Laboratory Press 2015-05 /pmc/articles/PMC4408805/ /pubmed/25805857 http://dx.doi.org/10.1261/rna.047985.114 Text en © 2015 Collins et al.; Published by Cold Spring Harbor Laboratory Press for the RNA Society http://creativecommons.org/licenses/by-nc/4.0/ This article is distributed exclusively by the RNA Society for the first 12 months after the full-issue publication date (see http://rnajournal.cshlp.org/site/misc/terms.xhtml). After 12 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 Articles
Collins, Richard A.
Stajich, Jason E.
Field, Deborah J.
Olive, Joan E.
DeAbreu, Diane M.
The low information content of Neurospora splicing signals: implications for RNA splicing and intron origin
title The low information content of Neurospora splicing signals: implications for RNA splicing and intron origin
title_full The low information content of Neurospora splicing signals: implications for RNA splicing and intron origin
title_fullStr The low information content of Neurospora splicing signals: implications for RNA splicing and intron origin
title_full_unstemmed The low information content of Neurospora splicing signals: implications for RNA splicing and intron origin
title_short The low information content of Neurospora splicing signals: implications for RNA splicing and intron origin
title_sort low information content of neurospora splicing signals: implications for rna splicing and intron origin
topic Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4408805/
https://www.ncbi.nlm.nih.gov/pubmed/25805857
http://dx.doi.org/10.1261/rna.047985.114
work_keys_str_mv AT collinsricharda thelowinformationcontentofneurosporasplicingsignalsimplicationsforrnasplicingandintronorigin
AT stajichjasone thelowinformationcontentofneurosporasplicingsignalsimplicationsforrnasplicingandintronorigin
AT fielddeborahj thelowinformationcontentofneurosporasplicingsignalsimplicationsforrnasplicingandintronorigin
AT olivejoane thelowinformationcontentofneurosporasplicingsignalsimplicationsforrnasplicingandintronorigin
AT deabreudianem thelowinformationcontentofneurosporasplicingsignalsimplicationsforrnasplicingandintronorigin
AT collinsricharda lowinformationcontentofneurosporasplicingsignalsimplicationsforrnasplicingandintronorigin
AT stajichjasone lowinformationcontentofneurosporasplicingsignalsimplicationsforrnasplicingandintronorigin
AT fielddeborahj lowinformationcontentofneurosporasplicingsignalsimplicationsforrnasplicingandintronorigin
AT olivejoane lowinformationcontentofneurosporasplicingsignalsimplicationsforrnasplicingandintronorigin
AT deabreudianem lowinformationcontentofneurosporasplicingsignalsimplicationsforrnasplicingandintronorigin