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Comparing the retention mechanisms of tandem duplicates and retrogenes in human and mouse genomes

BACKGROUND: Multiple models have been proposed to interpret the retention of duplicated genes. In this study, we attempted to compare whether the duplicates arising from tandem duplications and retropositions are retained by the same mechanisms in human and mouse genomes. RESULTS: Both sequence and...

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Autores principales: Wang, Zhen, Dong, Xiao, Ding, Guohui, Li, Yixue
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2902415/
https://www.ncbi.nlm.nih.gov/pubmed/20584267
http://dx.doi.org/10.1186/1297-9686-42-24
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author Wang, Zhen
Dong, Xiao
Ding, Guohui
Li, Yixue
author_facet Wang, Zhen
Dong, Xiao
Ding, Guohui
Li, Yixue
author_sort Wang, Zhen
collection PubMed
description BACKGROUND: Multiple models have been proposed to interpret the retention of duplicated genes. In this study, we attempted to compare whether the duplicates arising from tandem duplications and retropositions are retained by the same mechanisms in human and mouse genomes. RESULTS: Both sequence and expression similarity analyses revealed that tandem duplicates tend to be more conserved, whereas retrogenes tend to be more divergent. The duplicability of tandem duplicates is also higher than that of retrogenes. However, positive selection seems to play significant roles in the retention of both types of duplicates. CONCLUSIONS: We propose that dosage effect is more prevalent in the retention of tandem duplicates, while 'escape from adaptive conflict' (EAC) effect is more prevalent in the retention of retrogenes.
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spelling pubmed-29024152010-07-13 Comparing the retention mechanisms of tandem duplicates and retrogenes in human and mouse genomes Wang, Zhen Dong, Xiao Ding, Guohui Li, Yixue Genet Sel Evol Research BACKGROUND: Multiple models have been proposed to interpret the retention of duplicated genes. In this study, we attempted to compare whether the duplicates arising from tandem duplications and retropositions are retained by the same mechanisms in human and mouse genomes. RESULTS: Both sequence and expression similarity analyses revealed that tandem duplicates tend to be more conserved, whereas retrogenes tend to be more divergent. The duplicability of tandem duplicates is also higher than that of retrogenes. However, positive selection seems to play significant roles in the retention of both types of duplicates. CONCLUSIONS: We propose that dosage effect is more prevalent in the retention of tandem duplicates, while 'escape from adaptive conflict' (EAC) effect is more prevalent in the retention of retrogenes. BioMed Central 2010-06-28 /pmc/articles/PMC2902415/ /pubmed/20584267 http://dx.doi.org/10.1186/1297-9686-42-24 Text en Copyright ©2010 Wang 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
Wang, Zhen
Dong, Xiao
Ding, Guohui
Li, Yixue
Comparing the retention mechanisms of tandem duplicates and retrogenes in human and mouse genomes
title Comparing the retention mechanisms of tandem duplicates and retrogenes in human and mouse genomes
title_full Comparing the retention mechanisms of tandem duplicates and retrogenes in human and mouse genomes
title_fullStr Comparing the retention mechanisms of tandem duplicates and retrogenes in human and mouse genomes
title_full_unstemmed Comparing the retention mechanisms of tandem duplicates and retrogenes in human and mouse genomes
title_short Comparing the retention mechanisms of tandem duplicates and retrogenes in human and mouse genomes
title_sort comparing the retention mechanisms of tandem duplicates and retrogenes in human and mouse genomes
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2902415/
https://www.ncbi.nlm.nih.gov/pubmed/20584267
http://dx.doi.org/10.1186/1297-9686-42-24
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