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'Frankenstein genes', or the Mad Magazine version of the human pseudogenome

Annotation of the human genome is inching forward. Seven human chromosomes have now been fully annotated, covering 17 per cent of the genome, and at least one chromosome has been re-annotated. The enormity of the task forces a dependence on automated tools for detecting and assembling the genes, fol...

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Detalles Bibliográficos
Autor principal: Nelson, David R
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2004
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3525266/
https://www.ncbi.nlm.nih.gov/pubmed/15588491
http://dx.doi.org/10.1186/1479-7364-1-4-310
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author Nelson, David R
author_facet Nelson, David R
author_sort Nelson, David R
collection PubMed
description Annotation of the human genome is inching forward. Seven human chromosomes have now been fully annotated, covering 17 per cent of the genome, and at least one chromosome has been re-annotated. The enormity of the task forces a dependence on automated tools for detecting and assembling the genes, followed by hand curation to correct errors and polish the gene models. The accuracy of gene prediction algorithms is very good for internal exons from intact genes, but these programs do peculiar and exasperating things to pseudogenes. These programs can actually resurrect pseudogenes from the dead, making them into viable gene models for intact proteins, albeit science-fictional proteins. This process is demonstrated for four human pseudogenes from the cytochrome P450 family and one putatively functional P450 gene, CYP2U1, having a non-consensus intron boundary. These examples are offered as a call-to-arms to improve pseudogene prediction as an art in itself, and not as a by-product of gene annotation. Failure to do so will flood the databases with thousands of false-positive predictions. Indeed, they are already there.
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spelling pubmed-35252662012-12-19 'Frankenstein genes', or the Mad Magazine version of the human pseudogenome Nelson, David R Hum Genomics Genome Update Annotation of the human genome is inching forward. Seven human chromosomes have now been fully annotated, covering 17 per cent of the genome, and at least one chromosome has been re-annotated. The enormity of the task forces a dependence on automated tools for detecting and assembling the genes, followed by hand curation to correct errors and polish the gene models. The accuracy of gene prediction algorithms is very good for internal exons from intact genes, but these programs do peculiar and exasperating things to pseudogenes. These programs can actually resurrect pseudogenes from the dead, making them into viable gene models for intact proteins, albeit science-fictional proteins. This process is demonstrated for four human pseudogenes from the cytochrome P450 family and one putatively functional P450 gene, CYP2U1, having a non-consensus intron boundary. These examples are offered as a call-to-arms to improve pseudogene prediction as an art in itself, and not as a by-product of gene annotation. Failure to do so will flood the databases with thousands of false-positive predictions. Indeed, they are already there. BioMed Central 2004-05-01 /pmc/articles/PMC3525266/ /pubmed/15588491 http://dx.doi.org/10.1186/1479-7364-1-4-310 Text en Copyright ©2004 Henry Stewart Publications
spellingShingle Genome Update
Nelson, David R
'Frankenstein genes', or the Mad Magazine version of the human pseudogenome
title 'Frankenstein genes', or the Mad Magazine version of the human pseudogenome
title_full 'Frankenstein genes', or the Mad Magazine version of the human pseudogenome
title_fullStr 'Frankenstein genes', or the Mad Magazine version of the human pseudogenome
title_full_unstemmed 'Frankenstein genes', or the Mad Magazine version of the human pseudogenome
title_short 'Frankenstein genes', or the Mad Magazine version of the human pseudogenome
title_sort 'frankenstein genes', or the mad magazine version of the human pseudogenome
topic Genome Update
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3525266/
https://www.ncbi.nlm.nih.gov/pubmed/15588491
http://dx.doi.org/10.1186/1479-7364-1-4-310
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