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Evolution After Whole-Genome Duplication: A Network Perspective
Gene duplication plays an important role in the evolution of genomes and interactomes. Elucidating how evolution after gene duplication interplays at the sequence and network level is of great interest. In this work, we analyze a data set of gene pairs that arose through whole-genome duplication (WG...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Genetics Society of America
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3815064/ https://www.ncbi.nlm.nih.gov/pubmed/24048644 http://dx.doi.org/10.1534/g3.113.008458 |
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author | Zhu, Yun Lin, Zhenguo Nakhleh, Luay |
author_facet | Zhu, Yun Lin, Zhenguo Nakhleh, Luay |
author_sort | Zhu, Yun |
collection | PubMed |
description | Gene duplication plays an important role in the evolution of genomes and interactomes. Elucidating how evolution after gene duplication interplays at the sequence and network level is of great interest. In this work, we analyze a data set of gene pairs that arose through whole-genome duplication (WGD) in yeast. All these pairs have the same duplication time, making them ideal for evolutionary investigation. We investigated the interplay between evolution after WGD at the sequence and network levels and correlated these two levels of divergence with gene expression and fitness data. We find that molecular interactions involving WGD genes evolve at rates that are three orders of magnitude slower than the rates of evolution of the corresponding sequences. Furthermore, we find that divergence of WGD pairs correlates strongly with gene expression and fitness data. Because of the role of gene duplication in determining redundancy in biological systems and particularly at the network level, we investigated the role of interaction networks in elucidating the evolutionary fate of duplicated genes. We find that gene neighborhoods in interaction networks provide a mechanism for inferring these fates, and we developed an algorithm for achieving this task. Further epistasis analysis of WGD pairs categorized by their inferred evolutionary fates demonstrated the utility of these techniques. Finally, we find that WGD pairs and other pairs of paralogous genes of small-scale duplication origin share similar properties, giving good support for generalizing our results from WGD pairs to evolution after gene duplication in general. |
format | Online Article Text |
id | pubmed-3815064 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | Genetics Society of America |
record_format | MEDLINE/PubMed |
spelling | pubmed-38150642013-11-04 Evolution After Whole-Genome Duplication: A Network Perspective Zhu, Yun Lin, Zhenguo Nakhleh, Luay G3 (Bethesda) 6th Annual RECOMB/ISCB Conference on Regulatory & Systems Genomics Gene duplication plays an important role in the evolution of genomes and interactomes. Elucidating how evolution after gene duplication interplays at the sequence and network level is of great interest. In this work, we analyze a data set of gene pairs that arose through whole-genome duplication (WGD) in yeast. All these pairs have the same duplication time, making them ideal for evolutionary investigation. We investigated the interplay between evolution after WGD at the sequence and network levels and correlated these two levels of divergence with gene expression and fitness data. We find that molecular interactions involving WGD genes evolve at rates that are three orders of magnitude slower than the rates of evolution of the corresponding sequences. Furthermore, we find that divergence of WGD pairs correlates strongly with gene expression and fitness data. Because of the role of gene duplication in determining redundancy in biological systems and particularly at the network level, we investigated the role of interaction networks in elucidating the evolutionary fate of duplicated genes. We find that gene neighborhoods in interaction networks provide a mechanism for inferring these fates, and we developed an algorithm for achieving this task. Further epistasis analysis of WGD pairs categorized by their inferred evolutionary fates demonstrated the utility of these techniques. Finally, we find that WGD pairs and other pairs of paralogous genes of small-scale duplication origin share similar properties, giving good support for generalizing our results from WGD pairs to evolution after gene duplication in general. Genetics Society of America 2013-11-01 /pmc/articles/PMC3815064/ /pubmed/24048644 http://dx.doi.org/10.1534/g3.113.008458 Text en Copyright © 2013 Zhu et al. http://creativecommons.org/licenses/by/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution Unported License (http://creativecommons.org/licenses/by/3.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | 6th Annual RECOMB/ISCB Conference on Regulatory & Systems Genomics Zhu, Yun Lin, Zhenguo Nakhleh, Luay Evolution After Whole-Genome Duplication: A Network Perspective |
title | Evolution After Whole-Genome Duplication: A Network Perspective |
title_full | Evolution After Whole-Genome Duplication: A Network Perspective |
title_fullStr | Evolution After Whole-Genome Duplication: A Network Perspective |
title_full_unstemmed | Evolution After Whole-Genome Duplication: A Network Perspective |
title_short | Evolution After Whole-Genome Duplication: A Network Perspective |
title_sort | evolution after whole-genome duplication: a network perspective |
topic | 6th Annual RECOMB/ISCB Conference on Regulatory & Systems Genomics |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3815064/ https://www.ncbi.nlm.nih.gov/pubmed/24048644 http://dx.doi.org/10.1534/g3.113.008458 |
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