Cargando…

Evolution of Vertebrate Tissues Driven by Differential Modes of Gene Duplication

In this study, we investigated the evolution of vertebrate tissues by examining the potential association among gene expression, duplication, and base substitution patterns. In particular, we compared whole-genome duplication (WGD) with small-scale duplication (SSD), as well as tissue restricted wit...

Descripción completa

Detalles Bibliográficos
Autores principales: Satake, Masanobu, Kawata, Masakado, McLysaght, Aoife, Makino, Takashi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3415292/
https://www.ncbi.nlm.nih.gov/pubmed/22490996
http://dx.doi.org/10.1093/dnares/dss012
_version_ 1782240344854757376
author Satake, Masanobu
Kawata, Masakado
McLysaght, Aoife
Makino, Takashi
author_facet Satake, Masanobu
Kawata, Masakado
McLysaght, Aoife
Makino, Takashi
author_sort Satake, Masanobu
collection PubMed
description In this study, we investigated the evolution of vertebrate tissues by examining the potential association among gene expression, duplication, and base substitution patterns. In particular, we compared whole-genome duplication (WGD) with small-scale duplication (SSD), as well as tissue restricted with ubiquitously expressed genes. All patterns were also analysed in the light of gene evolutionary rates. Among those genes characterized by rapid evolution and expressed in a restricted range of tissues, SSD was represented in a larger proportion than WGD. Conversely, genes with ubiquitous expression were associated with slower evolutionary rates and a larger proportion of WGD. The results also show that evolutionary rates were faster in genes expressed in endodermal tissues and slower in ectodermal genes. Accordingly, the proportion of the SSD and WGD genes was highest in the endoderm and ectoderm, respectively. Therefore, quickly evolving SSD genes might have contributed to the faster evolution of endodermal tissues, whereas the comparatively slowly evolving WGD genes might have functioned to maintain the basic characteristics of ectodermal tissues. Mesenchymal tissues occupied an intermediate position in this regard, whereas the patterns observed for haemocytes were unique. Rapid tissue evolution could be related to a specific gene duplication mode (SSD) and faster molecular evolution in response to exposure to the external environment. These findings reveal general patterns underlying the evolution of tissues and their corresponding genes.
format Online
Article
Text
id pubmed-3415292
institution National Center for Biotechnology Information
language English
publishDate 2012
publisher Oxford University Press
record_format MEDLINE/PubMed
spelling pubmed-34152922012-08-09 Evolution of Vertebrate Tissues Driven by Differential Modes of Gene Duplication Satake, Masanobu Kawata, Masakado McLysaght, Aoife Makino, Takashi DNA Res Full Papers In this study, we investigated the evolution of vertebrate tissues by examining the potential association among gene expression, duplication, and base substitution patterns. In particular, we compared whole-genome duplication (WGD) with small-scale duplication (SSD), as well as tissue restricted with ubiquitously expressed genes. All patterns were also analysed in the light of gene evolutionary rates. Among those genes characterized by rapid evolution and expressed in a restricted range of tissues, SSD was represented in a larger proportion than WGD. Conversely, genes with ubiquitous expression were associated with slower evolutionary rates and a larger proportion of WGD. The results also show that evolutionary rates were faster in genes expressed in endodermal tissues and slower in ectodermal genes. Accordingly, the proportion of the SSD and WGD genes was highest in the endoderm and ectoderm, respectively. Therefore, quickly evolving SSD genes might have contributed to the faster evolution of endodermal tissues, whereas the comparatively slowly evolving WGD genes might have functioned to maintain the basic characteristics of ectodermal tissues. Mesenchymal tissues occupied an intermediate position in this regard, whereas the patterns observed for haemocytes were unique. Rapid tissue evolution could be related to a specific gene duplication mode (SSD) and faster molecular evolution in response to exposure to the external environment. These findings reveal general patterns underlying the evolution of tissues and their corresponding genes. Oxford University Press 2012-08 2012-04-05 /pmc/articles/PMC3415292/ /pubmed/22490996 http://dx.doi.org/10.1093/dnares/dss012 Text en © The Author 2012. Published by Oxford University Press on behalf of Kazusa DNA Research Institute http://creativecommons.org/licenses/by-nc/3.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0/), which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Full Papers
Satake, Masanobu
Kawata, Masakado
McLysaght, Aoife
Makino, Takashi
Evolution of Vertebrate Tissues Driven by Differential Modes of Gene Duplication
title Evolution of Vertebrate Tissues Driven by Differential Modes of Gene Duplication
title_full Evolution of Vertebrate Tissues Driven by Differential Modes of Gene Duplication
title_fullStr Evolution of Vertebrate Tissues Driven by Differential Modes of Gene Duplication
title_full_unstemmed Evolution of Vertebrate Tissues Driven by Differential Modes of Gene Duplication
title_short Evolution of Vertebrate Tissues Driven by Differential Modes of Gene Duplication
title_sort evolution of vertebrate tissues driven by differential modes of gene duplication
topic Full Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3415292/
https://www.ncbi.nlm.nih.gov/pubmed/22490996
http://dx.doi.org/10.1093/dnares/dss012
work_keys_str_mv AT satakemasanobu evolutionofvertebratetissuesdrivenbydifferentialmodesofgeneduplication
AT kawatamasakado evolutionofvertebratetissuesdrivenbydifferentialmodesofgeneduplication
AT mclysaghtaoife evolutionofvertebratetissuesdrivenbydifferentialmodesofgeneduplication
AT makinotakashi evolutionofvertebratetissuesdrivenbydifferentialmodesofgeneduplication