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Intron evolution in Neurospora: the role of mutational bias and selection

We used comparative and population genomics to study intron evolutionary dynamics in the fungal model genus Neurospora. For our investigation, we used well-annotated genomes of N. crassa, N. discreta, and N. tetrasperma, and 92 resequenced genomes of N. tetrasperma from natural populations. By analy...

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Autores principales: Sun, Yu, Whittle, Carrie A., Corcoran, Pádraic, Johannesson, Hanna
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/PMC4317165/
https://www.ncbi.nlm.nih.gov/pubmed/25342722
http://dx.doi.org/10.1101/gr.175653.114
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author Sun, Yu
Whittle, Carrie A.
Corcoran, Pádraic
Johannesson, Hanna
author_facet Sun, Yu
Whittle, Carrie A.
Corcoran, Pádraic
Johannesson, Hanna
author_sort Sun, Yu
collection PubMed
description We used comparative and population genomics to study intron evolutionary dynamics in the fungal model genus Neurospora. For our investigation, we used well-annotated genomes of N. crassa, N. discreta, and N. tetrasperma, and 92 resequenced genomes of N. tetrasperma from natural populations. By analyzing the four well-annotated genomes, we identified 9495 intron sites in 7619 orthologous genes. Our data supports nonhomologous end joining (NHEJ) and tandem duplication as mechanisms for intron gains in the genus and the RT-mRNA process as a mechanism for intron loss. We found a moderate intron gain rate (5.78–6.89 × 10(−13) intron gains per nucleotide site per year) and a high intron loss rate (7.53–13.76 × 10(−10) intron losses per intron sites per year) as compared to other eukaryotes. The derived intron gains and losses are skewed to high frequencies, relative to neutral SNPs, in natural populations of N. tetrasperma, suggesting that selection is involved in maintaining a high intron turnover. Furthermore, our analyses of the association between intron population-level frequency and genomic features suggest that selection is involved in shaping a 5′ intron position bias and a low intron GC content. However, intron sequence analyses suggest that the gained introns were not exposed to recent selective sweeps. Taken together, this work contributes to our understanding of the importance of mutational bias and selection in shaping the intron distribution in eukaryotic genomes.
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spelling pubmed-43171652015-07-01 Intron evolution in Neurospora: the role of mutational bias and selection Sun, Yu Whittle, Carrie A. Corcoran, Pádraic Johannesson, Hanna Genome Res Research We used comparative and population genomics to study intron evolutionary dynamics in the fungal model genus Neurospora. For our investigation, we used well-annotated genomes of N. crassa, N. discreta, and N. tetrasperma, and 92 resequenced genomes of N. tetrasperma from natural populations. By analyzing the four well-annotated genomes, we identified 9495 intron sites in 7619 orthologous genes. Our data supports nonhomologous end joining (NHEJ) and tandem duplication as mechanisms for intron gains in the genus and the RT-mRNA process as a mechanism for intron loss. We found a moderate intron gain rate (5.78–6.89 × 10(−13) intron gains per nucleotide site per year) and a high intron loss rate (7.53–13.76 × 10(−10) intron losses per intron sites per year) as compared to other eukaryotes. The derived intron gains and losses are skewed to high frequencies, relative to neutral SNPs, in natural populations of N. tetrasperma, suggesting that selection is involved in maintaining a high intron turnover. Furthermore, our analyses of the association between intron population-level frequency and genomic features suggest that selection is involved in shaping a 5′ intron position bias and a low intron GC content. However, intron sequence analyses suggest that the gained introns were not exposed to recent selective sweeps. Taken together, this work contributes to our understanding of the importance of mutational bias and selection in shaping the intron distribution in eukaryotic genomes. Cold Spring Harbor Laboratory Press 2015-01 /pmc/articles/PMC4317165/ /pubmed/25342722 http://dx.doi.org/10.1101/gr.175653.114 Text en © 2015 Sun et al.; Published by Cold Spring Harbor Laboratory Press http://creativecommons.org/licenses/by-nc/4.0/ This article is distributed exclusively by Cold Spring Harbor Laboratory Press for the first six months after the full-issue publication date (see http://genome.cshlp.org/site/misc/terms.xhtml). After six 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 Research
Sun, Yu
Whittle, Carrie A.
Corcoran, Pádraic
Johannesson, Hanna
Intron evolution in Neurospora: the role of mutational bias and selection
title Intron evolution in Neurospora: the role of mutational bias and selection
title_full Intron evolution in Neurospora: the role of mutational bias and selection
title_fullStr Intron evolution in Neurospora: the role of mutational bias and selection
title_full_unstemmed Intron evolution in Neurospora: the role of mutational bias and selection
title_short Intron evolution in Neurospora: the role of mutational bias and selection
title_sort intron evolution in neurospora: the role of mutational bias and selection
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4317165/
https://www.ncbi.nlm.nih.gov/pubmed/25342722
http://dx.doi.org/10.1101/gr.175653.114
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