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Complex fate of paralogs
BACKGROUND: Thanks to recent high coverage mass-spectrometry studies and reconstructed protein complexes, we are now in an unprecedented position to study the evolution of biological systems. Gene duplications, known to be a major source of innovation in evolution, can now be readily examined in the...
Autores principales: | , , |
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Formato: | Texto |
Lenguaje: | English |
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BioMed Central
2008
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2628386/ https://www.ncbi.nlm.nih.gov/pubmed/19094234 http://dx.doi.org/10.1186/1471-2148-8-337 |
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author | Szklarczyk, Radek Huynen, Martijn A Snel, Berend |
author_facet | Szklarczyk, Radek Huynen, Martijn A Snel, Berend |
author_sort | Szklarczyk, Radek |
collection | PubMed |
description | BACKGROUND: Thanks to recent high coverage mass-spectrometry studies and reconstructed protein complexes, we are now in an unprecedented position to study the evolution of biological systems. Gene duplications, known to be a major source of innovation in evolution, can now be readily examined in the context of protein complexes. RESULTS: We observe that paralogs operating in the same complex fulfill different roles: mRNA dosage increase for more than a hundred cytosolic ribosomal proteins, mutually exclusive participation of at least 54 paralogs resulting in alternative forms of complexes, and 24 proteins contributing to bona fide structural growth. Inspection of paralogous proteins participating in two independent complexes shows that an ancient, pre-duplication protein functioned in both multi-protein assemblies and a gene duplication event allowed the respective copies to specialize and split their roles. CONCLUSION: Variants with conditionally assembled, paralogous subunits likely have played a role in yeast's adaptation to anaerobic conditions. In a number of cases the gene duplication has given rise to one duplicate that is no longer part of a protein complex and shows an accelerated rate of evolution. Such genes could provide the raw material for the evolution of new functions. |
format | Text |
id | pubmed-2628386 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2008 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-26283862009-01-17 Complex fate of paralogs Szklarczyk, Radek Huynen, Martijn A Snel, Berend BMC Evol Biol Research Article BACKGROUND: Thanks to recent high coverage mass-spectrometry studies and reconstructed protein complexes, we are now in an unprecedented position to study the evolution of biological systems. Gene duplications, known to be a major source of innovation in evolution, can now be readily examined in the context of protein complexes. RESULTS: We observe that paralogs operating in the same complex fulfill different roles: mRNA dosage increase for more than a hundred cytosolic ribosomal proteins, mutually exclusive participation of at least 54 paralogs resulting in alternative forms of complexes, and 24 proteins contributing to bona fide structural growth. Inspection of paralogous proteins participating in two independent complexes shows that an ancient, pre-duplication protein functioned in both multi-protein assemblies and a gene duplication event allowed the respective copies to specialize and split their roles. CONCLUSION: Variants with conditionally assembled, paralogous subunits likely have played a role in yeast's adaptation to anaerobic conditions. In a number of cases the gene duplication has given rise to one duplicate that is no longer part of a protein complex and shows an accelerated rate of evolution. Such genes could provide the raw material for the evolution of new functions. BioMed Central 2008-12-18 /pmc/articles/PMC2628386/ /pubmed/19094234 http://dx.doi.org/10.1186/1471-2148-8-337 Text en Copyright ©2008 Szklarczyk et al; 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 Szklarczyk, Radek Huynen, Martijn A Snel, Berend Complex fate of paralogs |
title | Complex fate of paralogs |
title_full | Complex fate of paralogs |
title_fullStr | Complex fate of paralogs |
title_full_unstemmed | Complex fate of paralogs |
title_short | Complex fate of paralogs |
title_sort | complex fate of paralogs |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2628386/ https://www.ncbi.nlm.nih.gov/pubmed/19094234 http://dx.doi.org/10.1186/1471-2148-8-337 |
work_keys_str_mv | AT szklarczykradek complexfateofparalogs AT huynenmartijna complexfateofparalogs AT snelberend complexfateofparalogs |