Fast rate of evolution in alternatively spliced coding regions of mammalian genes

<p>Abstract</p> <p>Background</p> <p>At least half of mammalian genes are alternatively spliced. Alternative isoforms are often genome-specific and it has been suggested that alternative splicing is one of the major mechanisms for generating protein diversity in the cou...

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Main Authors: Nurtdinov Ramil N, Ermakova Ekaterina O, Gelfand Mikhail S
Format: Article
Language:English
Published: BMC 2006-04-01
Series:BMC Genomics
Online Access:http://www.biomedcentral.com/1471-2164/7/84
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spelling doaj-32ccebdc71ac48a2b037e23a0ae45ac62020-11-25T02:26:31ZengBMCBMC Genomics1471-21642006-04-01718410.1186/1471-2164-7-84Fast rate of evolution in alternatively spliced coding regions of mammalian genesNurtdinov Ramil NErmakova Ekaterina OGelfand Mikhail S<p>Abstract</p> <p>Background</p> <p>At least half of mammalian genes are alternatively spliced. Alternative isoforms are often genome-specific and it has been suggested that alternative splicing is one of the major mechanisms for generating protein diversity in the course of evolution. Another way of looking at alternative splicing is to consider sequence evolution of constitutive and alternative regions of protein-coding genes. Indeed, it turns out that constitutive and alternative regions evolve in different ways.</p> <p>Results</p> <p>A set of 3029 orthologous pairs of human and mouse alternatively spliced genes was considered. The rate of nonsynonymous substitutions (d<sub>N</sub>), the rate of synonymous substitutions (d<sub>S</sub>), and their ratio (ω = d<sub>N</sub>/d<sub>S</sub>) appear to be significantly higher in alternatively spliced coding regions compared to constitutive regions. When N-terminal, internal and C-terminal alternatives are analysed separately, C-terminal alternatives appear to make the main contribution to the observed difference. The effects become even more pronounced in a subset of fast evolving genes.</p> <p>Conclusion</p> <p>These results provide evidence of weaker purifying selection and/or stronger positive selection in alternative regions and thus one more confirmation of accelerated evolution in alternative regions. This study corroborates the theory that alternative splicing serves as a testing ground for molecular evolution.</p> http://www.biomedcentral.com/1471-2164/7/84
collection DOAJ
language English
format Article
sources DOAJ
author Nurtdinov Ramil N
Ermakova Ekaterina O
Gelfand Mikhail S
spellingShingle Nurtdinov Ramil N
Ermakova Ekaterina O
Gelfand Mikhail S
Fast rate of evolution in alternatively spliced coding regions of mammalian genes
BMC Genomics
author_facet Nurtdinov Ramil N
Ermakova Ekaterina O
Gelfand Mikhail S
author_sort Nurtdinov Ramil N
title Fast rate of evolution in alternatively spliced coding regions of mammalian genes
title_short Fast rate of evolution in alternatively spliced coding regions of mammalian genes
title_full Fast rate of evolution in alternatively spliced coding regions of mammalian genes
title_fullStr Fast rate of evolution in alternatively spliced coding regions of mammalian genes
title_full_unstemmed Fast rate of evolution in alternatively spliced coding regions of mammalian genes
title_sort fast rate of evolution in alternatively spliced coding regions of mammalian genes
publisher BMC
series BMC Genomics
issn 1471-2164
publishDate 2006-04-01
description <p>Abstract</p> <p>Background</p> <p>At least half of mammalian genes are alternatively spliced. Alternative isoforms are often genome-specific and it has been suggested that alternative splicing is one of the major mechanisms for generating protein diversity in the course of evolution. Another way of looking at alternative splicing is to consider sequence evolution of constitutive and alternative regions of protein-coding genes. Indeed, it turns out that constitutive and alternative regions evolve in different ways.</p> <p>Results</p> <p>A set of 3029 orthologous pairs of human and mouse alternatively spliced genes was considered. The rate of nonsynonymous substitutions (d<sub>N</sub>), the rate of synonymous substitutions (d<sub>S</sub>), and their ratio (ω = d<sub>N</sub>/d<sub>S</sub>) appear to be significantly higher in alternatively spliced coding regions compared to constitutive regions. When N-terminal, internal and C-terminal alternatives are analysed separately, C-terminal alternatives appear to make the main contribution to the observed difference. The effects become even more pronounced in a subset of fast evolving genes.</p> <p>Conclusion</p> <p>These results provide evidence of weaker purifying selection and/or stronger positive selection in alternative regions and thus one more confirmation of accelerated evolution in alternative regions. This study corroborates the theory that alternative splicing serves as a testing ground for molecular evolution.</p>
url http://www.biomedcentral.com/1471-2164/7/84
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