Local synteny and codon usage contribute to asymmetric sequence divergence of <it>Saccharomyces cerevisiae </it>gene duplicates

<p>Abstract</p> <p>Background</p> <p>Duplicated genes frequently experience asymmetric rates of sequence evolution. Relaxed selective constraints and positive selection have both been invoked to explain the observation that one paralog within a gene-duplicate pair exhib...

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Main Authors: Bergthorsson Ulfar, Bu Lijing, Katju Vaishali
Format: Article
Language:English
Published: BMC 2011-09-01
Series:BMC Evolutionary Biology
Online Access:http://www.biomedcentral.com/1471-2148/11/279
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spelling doaj-0cccfb80dd9943d99749ac7e504fca0e2021-09-02T10:06:36ZengBMCBMC Evolutionary Biology1471-21482011-09-0111127910.1186/1471-2148-11-279Local synteny and codon usage contribute to asymmetric sequence divergence of <it>Saccharomyces cerevisiae </it>gene duplicatesBergthorsson UlfarBu LijingKatju Vaishali<p>Abstract</p> <p>Background</p> <p>Duplicated genes frequently experience asymmetric rates of sequence evolution. Relaxed selective constraints and positive selection have both been invoked to explain the observation that one paralog within a gene-duplicate pair exhibits an accelerated rate of sequence evolution. In the majority of studies where asymmetric divergence has been established, there is no indication as to which gene copy, ancestral or derived, is evolving more rapidly. In this study we investigated the effect of local synteny (gene-neighborhood conservation) and codon usage on the sequence evolution of gene duplicates in the <it>S. cerevisiae </it>genome. We further distinguish the gene duplicates into those that originated from a whole-genome duplication (WGD) event (ohnologs) versus small-scale duplications (SSD) to determine if there exist any differences in their patterns of sequence evolution.</p> <p>Results</p> <p>For SSD pairs, the derived copy evolves faster than the ancestral copy. However, there is no relationship between rate asymmetry and synteny conservation (ancestral-like <it>versus </it>derived-like) in ohnologs. mRNA abundance and optimal codon usage as measured by the CAI is lower in the derived SSD copies relative to ancestral paralogs. Moreover, in the case of ohnologs, the faster-evolving copy has lower CAI and lowered expression.</p> <p>Conclusions</p> <p>Together, these results suggest that relaxation of selection for codon usage and gene expression contribute to rate asymmetry in the evolution of duplicated genes and that in SSD pairs, the relaxation of selection stems from the loss of ancestral regulatory information in the derived copy.</p> http://www.biomedcentral.com/1471-2148/11/279
collection DOAJ
language English
format Article
sources DOAJ
author Bergthorsson Ulfar
Bu Lijing
Katju Vaishali
spellingShingle Bergthorsson Ulfar
Bu Lijing
Katju Vaishali
Local synteny and codon usage contribute to asymmetric sequence divergence of <it>Saccharomyces cerevisiae </it>gene duplicates
BMC Evolutionary Biology
author_facet Bergthorsson Ulfar
Bu Lijing
Katju Vaishali
author_sort Bergthorsson Ulfar
title Local synteny and codon usage contribute to asymmetric sequence divergence of <it>Saccharomyces cerevisiae </it>gene duplicates
title_short Local synteny and codon usage contribute to asymmetric sequence divergence of <it>Saccharomyces cerevisiae </it>gene duplicates
title_full Local synteny and codon usage contribute to asymmetric sequence divergence of <it>Saccharomyces cerevisiae </it>gene duplicates
title_fullStr Local synteny and codon usage contribute to asymmetric sequence divergence of <it>Saccharomyces cerevisiae </it>gene duplicates
title_full_unstemmed Local synteny and codon usage contribute to asymmetric sequence divergence of <it>Saccharomyces cerevisiae </it>gene duplicates
title_sort local synteny and codon usage contribute to asymmetric sequence divergence of <it>saccharomyces cerevisiae </it>gene duplicates
publisher BMC
series BMC Evolutionary Biology
issn 1471-2148
publishDate 2011-09-01
description <p>Abstract</p> <p>Background</p> <p>Duplicated genes frequently experience asymmetric rates of sequence evolution. Relaxed selective constraints and positive selection have both been invoked to explain the observation that one paralog within a gene-duplicate pair exhibits an accelerated rate of sequence evolution. In the majority of studies where asymmetric divergence has been established, there is no indication as to which gene copy, ancestral or derived, is evolving more rapidly. In this study we investigated the effect of local synteny (gene-neighborhood conservation) and codon usage on the sequence evolution of gene duplicates in the <it>S. cerevisiae </it>genome. We further distinguish the gene duplicates into those that originated from a whole-genome duplication (WGD) event (ohnologs) versus small-scale duplications (SSD) to determine if there exist any differences in their patterns of sequence evolution.</p> <p>Results</p> <p>For SSD pairs, the derived copy evolves faster than the ancestral copy. However, there is no relationship between rate asymmetry and synteny conservation (ancestral-like <it>versus </it>derived-like) in ohnologs. mRNA abundance and optimal codon usage as measured by the CAI is lower in the derived SSD copies relative to ancestral paralogs. Moreover, in the case of ohnologs, the faster-evolving copy has lower CAI and lowered expression.</p> <p>Conclusions</p> <p>Together, these results suggest that relaxation of selection for codon usage and gene expression contribute to rate asymmetry in the evolution of duplicated genes and that in SSD pairs, the relaxation of selection stems from the loss of ancestral regulatory information in the derived copy.</p>
url http://www.biomedcentral.com/1471-2148/11/279
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