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Functional divergence of gene duplicates – a domain-centric view
BACKGROUND: Gene duplicates have been shown to evolve at different rates. Here we further investigate the mechanism and functional underpinning of this phenomenon by assessing asymmetric evolution specifically within functional domains of gene duplicates. RESULTS: Based on duplicate genes in five te...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2012
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3426493/ https://www.ncbi.nlm.nih.gov/pubmed/22839301 http://dx.doi.org/10.1186/1471-2148-12-126 |
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author | Khaladkar, Mugdha Hannenhalli, Sridhar |
author_facet | Khaladkar, Mugdha Hannenhalli, Sridhar |
author_sort | Khaladkar, Mugdha |
collection | PubMed |
description | BACKGROUND: Gene duplicates have been shown to evolve at different rates. Here we further investigate the mechanism and functional underpinning of this phenomenon by assessing asymmetric evolution specifically within functional domains of gene duplicates. RESULTS: Based on duplicate genes in five teleost fishes resulting from a whole genome duplication event, we first show that a Fisher Exact test based approach to detect asymmetry is more sensitive than the previously used Likelihood Ratio test. Using our Fisher Exact test, we found that the evolutionary rate asymmetry in the overall protein is largely explained by the asymmetric evolution within specific protein domains. Moreover, among cases of asymmetrically evolving domains, for the gene copy containing a fast evolving domain, the non-synonymous substitutions often cluster within the fast evolving domain. We found that rare substitutions were preferred within asymmetrically evolving domains suggestive of functional divergence. While overall ~32 % of the domains tested were found to be evolving asymmetrically, certain protein domains such as the Tyrosine and Ser/Thr Kinase domains had a much greater prevalence of asymmetric evolution. Finally, based on the spatial expression of Zebra fish duplicate proteins during development, we found that protein pairs containing asymmetrically evolving domains had a greater divergence in gene expression as compared to the duplicate proteins that did not exhibit asymmetric evolution. CONCLUSIONS: Taken together, our results suggest that the previously observed asymmetry in the overall duplicate protein evolution is largely due to divergence of specific domains of the protein, and coincides with divergence in spatial expression domains. |
format | Online Article Text |
id | pubmed-3426493 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-34264932012-08-24 Functional divergence of gene duplicates – a domain-centric view Khaladkar, Mugdha Hannenhalli, Sridhar BMC Evol Biol Research Article BACKGROUND: Gene duplicates have been shown to evolve at different rates. Here we further investigate the mechanism and functional underpinning of this phenomenon by assessing asymmetric evolution specifically within functional domains of gene duplicates. RESULTS: Based on duplicate genes in five teleost fishes resulting from a whole genome duplication event, we first show that a Fisher Exact test based approach to detect asymmetry is more sensitive than the previously used Likelihood Ratio test. Using our Fisher Exact test, we found that the evolutionary rate asymmetry in the overall protein is largely explained by the asymmetric evolution within specific protein domains. Moreover, among cases of asymmetrically evolving domains, for the gene copy containing a fast evolving domain, the non-synonymous substitutions often cluster within the fast evolving domain. We found that rare substitutions were preferred within asymmetrically evolving domains suggestive of functional divergence. While overall ~32 % of the domains tested were found to be evolving asymmetrically, certain protein domains such as the Tyrosine and Ser/Thr Kinase domains had a much greater prevalence of asymmetric evolution. Finally, based on the spatial expression of Zebra fish duplicate proteins during development, we found that protein pairs containing asymmetrically evolving domains had a greater divergence in gene expression as compared to the duplicate proteins that did not exhibit asymmetric evolution. CONCLUSIONS: Taken together, our results suggest that the previously observed asymmetry in the overall duplicate protein evolution is largely due to divergence of specific domains of the protein, and coincides with divergence in spatial expression domains. BioMed Central 2012-07-27 /pmc/articles/PMC3426493/ /pubmed/22839301 http://dx.doi.org/10.1186/1471-2148-12-126 Text en Copyright ©2012 Khaladkar and Hannenhalli; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Article Khaladkar, Mugdha Hannenhalli, Sridhar Functional divergence of gene duplicates – a domain-centric view |
title | Functional divergence of gene duplicates – a domain-centric view |
title_full | Functional divergence of gene duplicates – a domain-centric view |
title_fullStr | Functional divergence of gene duplicates – a domain-centric view |
title_full_unstemmed | Functional divergence of gene duplicates – a domain-centric view |
title_short | Functional divergence of gene duplicates – a domain-centric view |
title_sort | functional divergence of gene duplicates – a domain-centric view |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3426493/ https://www.ncbi.nlm.nih.gov/pubmed/22839301 http://dx.doi.org/10.1186/1471-2148-12-126 |
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