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Identification and analysis of unitary pseudogenes: historic and contemporary gene losses in humans and other primates

BACKGROUND: Unitary pseudogenes are a class of unprocessed pseudogenes without functioning counterparts in the genome. They constitute only a small fraction of annotated pseudogenes in the human genome. However, as they represent distinct functional losses over time, they shed light on the unique fe...

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Autores principales: Zhang, Zhengdong D, Frankish, Adam, Hunt, Toby, Harrow, Jennifer, Gerstein, Mark
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2864566/
https://www.ncbi.nlm.nih.gov/pubmed/20210993
http://dx.doi.org/10.1186/gb-2010-11-3-r26
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author Zhang, Zhengdong D
Frankish, Adam
Hunt, Toby
Harrow, Jennifer
Gerstein, Mark
author_facet Zhang, Zhengdong D
Frankish, Adam
Hunt, Toby
Harrow, Jennifer
Gerstein, Mark
author_sort Zhang, Zhengdong D
collection PubMed
description BACKGROUND: Unitary pseudogenes are a class of unprocessed pseudogenes without functioning counterparts in the genome. They constitute only a small fraction of annotated pseudogenes in the human genome. However, as they represent distinct functional losses over time, they shed light on the unique features of humans in primate evolution. RESULTS: We have developed a pipeline to detect human unitary pseudogenes through analyzing the global inventory of orthologs between the human genome and its mammalian relatives. We focus on gene losses along the human lineage after the divergence from rodents about 75 million years ago. In total, we identify 76 unitary pseudogenes, including previously annotated ones, and many novel ones. By comparing each of these to its functioning ortholog in other mammals, we can approximately date the creation of each unitary pseudogene (that is, the gene 'death date') and show that for our group of 76, the functional genes appear to be disabled at a fairly uniform rate throughout primate evolution - not all at once, correlated, for instance, with the 'Alu burst'. Furthermore, we identify 11 unitary pseudogenes that are polymorphic - that is, they have both nonfunctional and functional alleles currently segregating in the human population. Comparing them with their orthologs in other primates, we find that two of them are in fact pseudogenes in non-human primates, suggesting that they represent cases of a gene being resurrected in the human lineage. CONCLUSIONS: This analysis of unitary pseudogenes provides insights into the evolutionary constraints faced by different organisms and the timescales of functional gene loss in humans.
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spelling pubmed-28645662010-05-05 Identification and analysis of unitary pseudogenes: historic and contemporary gene losses in humans and other primates Zhang, Zhengdong D Frankish, Adam Hunt, Toby Harrow, Jennifer Gerstein, Mark Genome Biol Research BACKGROUND: Unitary pseudogenes are a class of unprocessed pseudogenes without functioning counterparts in the genome. They constitute only a small fraction of annotated pseudogenes in the human genome. However, as they represent distinct functional losses over time, they shed light on the unique features of humans in primate evolution. RESULTS: We have developed a pipeline to detect human unitary pseudogenes through analyzing the global inventory of orthologs between the human genome and its mammalian relatives. We focus on gene losses along the human lineage after the divergence from rodents about 75 million years ago. In total, we identify 76 unitary pseudogenes, including previously annotated ones, and many novel ones. By comparing each of these to its functioning ortholog in other mammals, we can approximately date the creation of each unitary pseudogene (that is, the gene 'death date') and show that for our group of 76, the functional genes appear to be disabled at a fairly uniform rate throughout primate evolution - not all at once, correlated, for instance, with the 'Alu burst'. Furthermore, we identify 11 unitary pseudogenes that are polymorphic - that is, they have both nonfunctional and functional alleles currently segregating in the human population. Comparing them with their orthologs in other primates, we find that two of them are in fact pseudogenes in non-human primates, suggesting that they represent cases of a gene being resurrected in the human lineage. CONCLUSIONS: This analysis of unitary pseudogenes provides insights into the evolutionary constraints faced by different organisms and the timescales of functional gene loss in humans. BioMed Central 2010 2010-03-08 /pmc/articles/PMC2864566/ /pubmed/20210993 http://dx.doi.org/10.1186/gb-2010-11-3-r26 Text en Copyright ©2010 Zhang 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
Zhang, Zhengdong D
Frankish, Adam
Hunt, Toby
Harrow, Jennifer
Gerstein, Mark
Identification and analysis of unitary pseudogenes: historic and contemporary gene losses in humans and other primates
title Identification and analysis of unitary pseudogenes: historic and contemporary gene losses in humans and other primates
title_full Identification and analysis of unitary pseudogenes: historic and contemporary gene losses in humans and other primates
title_fullStr Identification and analysis of unitary pseudogenes: historic and contemporary gene losses in humans and other primates
title_full_unstemmed Identification and analysis of unitary pseudogenes: historic and contemporary gene losses in humans and other primates
title_short Identification and analysis of unitary pseudogenes: historic and contemporary gene losses in humans and other primates
title_sort identification and analysis of unitary pseudogenes: historic and contemporary gene losses in humans and other primates
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2864566/
https://www.ncbi.nlm.nih.gov/pubmed/20210993
http://dx.doi.org/10.1186/gb-2010-11-3-r26
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