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Not so pseudo: the evolutionary history of protein phosphatase 1 regulatory subunit 2 and related pseudogenes

BACKGROUND: Pseudogenes are traditionally considered “dead” genes, therefore lacking biological functions. This view has however been challenged during the last decade. This is the case of the Protein phosphatase 1 regulatory subunit 2 (PPP1R2) or inhibitor-2 gene family, for which several incomplet...

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Autores principales: Korrodi-Gregório, Luís, Abrantes, Joana, Muller, Thorsten, Melo-Ferreira, José, Marcus, Katrin, da Cruz e Silva, Odete AB, Fardilha, Margarida, Esteves, Pedro J
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3840573/
https://www.ncbi.nlm.nih.gov/pubmed/24195737
http://dx.doi.org/10.1186/1471-2148-13-242
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author Korrodi-Gregório, Luís
Abrantes, Joana
Muller, Thorsten
Melo-Ferreira, José
Marcus, Katrin
da Cruz e Silva, Odete AB
Fardilha, Margarida
Esteves, Pedro J
author_facet Korrodi-Gregório, Luís
Abrantes, Joana
Muller, Thorsten
Melo-Ferreira, José
Marcus, Katrin
da Cruz e Silva, Odete AB
Fardilha, Margarida
Esteves, Pedro J
author_sort Korrodi-Gregório, Luís
collection PubMed
description BACKGROUND: Pseudogenes are traditionally considered “dead” genes, therefore lacking biological functions. This view has however been challenged during the last decade. This is the case of the Protein phosphatase 1 regulatory subunit 2 (PPP1R2) or inhibitor-2 gene family, for which several incomplete copies exist scattered throughout the genome. RESULTS: In this study, the pseudogenization process of PPP1R2 was analyzed. Ten PPP1R2-related pseudogenes (PPP1R2P1-P10), highly similar to PPP1R2, were retrieved from the human genome assembly present in the databases. The phylogenetic analysis of mammalian PPP1R2 and related pseudogenes suggested that PPP1R2P7 and PPP1R2P9 retroposons appeared before the great mammalian radiation, while the remaining pseudogenes are primate-specific and retroposed at different times during Primate evolution. Although considered inactive, four of these pseudogenes seem to be transcribed and possibly possess biological functions. Given the role of PPP1R2 in sperm motility, the presence of these proteins was assessed in human sperm, and two PPP1R2-related proteins were detected, PPP1R2P3 and PPP1R2P9. Signatures of negative and positive selection were also detected in PPP1R2P9, further suggesting a role as a functional protein. CONCLUSIONS: The results show that contrary to initial observations PPP1R2-related pseudogenes are not simple bystanders of the evolutionary process but may rather be at the origin of genes with novel functions.
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spelling pubmed-38405732013-11-27 Not so pseudo: the evolutionary history of protein phosphatase 1 regulatory subunit 2 and related pseudogenes Korrodi-Gregório, Luís Abrantes, Joana Muller, Thorsten Melo-Ferreira, José Marcus, Katrin da Cruz e Silva, Odete AB Fardilha, Margarida Esteves, Pedro J BMC Evol Biol Research Article BACKGROUND: Pseudogenes are traditionally considered “dead” genes, therefore lacking biological functions. This view has however been challenged during the last decade. This is the case of the Protein phosphatase 1 regulatory subunit 2 (PPP1R2) or inhibitor-2 gene family, for which several incomplete copies exist scattered throughout the genome. RESULTS: In this study, the pseudogenization process of PPP1R2 was analyzed. Ten PPP1R2-related pseudogenes (PPP1R2P1-P10), highly similar to PPP1R2, were retrieved from the human genome assembly present in the databases. The phylogenetic analysis of mammalian PPP1R2 and related pseudogenes suggested that PPP1R2P7 and PPP1R2P9 retroposons appeared before the great mammalian radiation, while the remaining pseudogenes are primate-specific and retroposed at different times during Primate evolution. Although considered inactive, four of these pseudogenes seem to be transcribed and possibly possess biological functions. Given the role of PPP1R2 in sperm motility, the presence of these proteins was assessed in human sperm, and two PPP1R2-related proteins were detected, PPP1R2P3 and PPP1R2P9. Signatures of negative and positive selection were also detected in PPP1R2P9, further suggesting a role as a functional protein. CONCLUSIONS: The results show that contrary to initial observations PPP1R2-related pseudogenes are not simple bystanders of the evolutionary process but may rather be at the origin of genes with novel functions. BioMed Central 2013-11-06 /pmc/articles/PMC3840573/ /pubmed/24195737 http://dx.doi.org/10.1186/1471-2148-13-242 Text en Copyright © 2013 Korrodi-Gregório 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
Korrodi-Gregório, Luís
Abrantes, Joana
Muller, Thorsten
Melo-Ferreira, José
Marcus, Katrin
da Cruz e Silva, Odete AB
Fardilha, Margarida
Esteves, Pedro J
Not so pseudo: the evolutionary history of protein phosphatase 1 regulatory subunit 2 and related pseudogenes
title Not so pseudo: the evolutionary history of protein phosphatase 1 regulatory subunit 2 and related pseudogenes
title_full Not so pseudo: the evolutionary history of protein phosphatase 1 regulatory subunit 2 and related pseudogenes
title_fullStr Not so pseudo: the evolutionary history of protein phosphatase 1 regulatory subunit 2 and related pseudogenes
title_full_unstemmed Not so pseudo: the evolutionary history of protein phosphatase 1 regulatory subunit 2 and related pseudogenes
title_short Not so pseudo: the evolutionary history of protein phosphatase 1 regulatory subunit 2 and related pseudogenes
title_sort not so pseudo: the evolutionary history of protein phosphatase 1 regulatory subunit 2 and related pseudogenes
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3840573/
https://www.ncbi.nlm.nih.gov/pubmed/24195737
http://dx.doi.org/10.1186/1471-2148-13-242
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