Comparative genomics search for losses of long-established genes on the human lineage.

Taking advantage of the complete genome sequences of several mammals, we developed a novel method to detect losses of well-established genes in the human genome through syntenic mapping of gene structures between the human, mouse, and dog genomes. Unlike most previous genomic methods for pseudogene...

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Main Authors: Jingchun Zhu, J Zachary Sanborn, Mark Diekhans, Craig B Lowe, Tom H Pringle, David Haussler
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2007-12-01
Series:PLoS Computational Biology
Online Access:https://doi.org/10.1371/journal.pcbi.0030247
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spelling doaj-cfa9ec0326204710889b5fcf5e2258992021-04-21T15:21:09ZengPublic Library of Science (PLoS)PLoS Computational Biology1553-734X1553-73582007-12-01312e24710.1371/journal.pcbi.0030247Comparative genomics search for losses of long-established genes on the human lineage.Jingchun ZhuJ Zachary SanbornMark DiekhansCraig B LoweTom H PringleDavid HausslerTaking advantage of the complete genome sequences of several mammals, we developed a novel method to detect losses of well-established genes in the human genome through syntenic mapping of gene structures between the human, mouse, and dog genomes. Unlike most previous genomic methods for pseudogene identification, this analysis is able to differentiate losses of well-established genes from pseudogenes formed shortly after segmental duplication or generated via retrotransposition. Therefore, it enables us to find genes that were inactivated long after their birth, which were likely to have evolved nonredundant biological functions before being inactivated. The method was used to look for gene losses along the human lineage during the approximately 75 million years (My) since the common ancestor of primates and rodents (the euarchontoglire crown group). We identified 26 losses of well-established genes in the human genome that were all lost at least 50 My after their birth. Many of them were previously characterized pseudogenes in the human genome, such as GULO and UOX. Our methodology is highly effective at identifying losses of single-copy genes of ancient origin, allowing us to find a few well-known pseudogenes in the human genome missed by previous high-throughput genome-wide studies. In addition to confirming previously known gene losses, we identified 16 previously uncharacterized human pseudogenes that are definitive losses of long-established genes. Among them is ACYL3, an ancient enzyme present in archaea, bacteria, and eukaryotes, but lost approximately 6 to 8 Mya in the ancestor of humans and chimps. Although losses of well-established genes do not equate to adaptive gene losses, they are a useful proxy to use when searching for such genetic changes. This is especially true for adaptive losses that occurred more than 250,000 years ago, since any genetic evidence of the selective sweep indicative of such an event has been erased.https://doi.org/10.1371/journal.pcbi.0030247
collection DOAJ
language English
format Article
sources DOAJ
author Jingchun Zhu
J Zachary Sanborn
Mark Diekhans
Craig B Lowe
Tom H Pringle
David Haussler
spellingShingle Jingchun Zhu
J Zachary Sanborn
Mark Diekhans
Craig B Lowe
Tom H Pringle
David Haussler
Comparative genomics search for losses of long-established genes on the human lineage.
PLoS Computational Biology
author_facet Jingchun Zhu
J Zachary Sanborn
Mark Diekhans
Craig B Lowe
Tom H Pringle
David Haussler
author_sort Jingchun Zhu
title Comparative genomics search for losses of long-established genes on the human lineage.
title_short Comparative genomics search for losses of long-established genes on the human lineage.
title_full Comparative genomics search for losses of long-established genes on the human lineage.
title_fullStr Comparative genomics search for losses of long-established genes on the human lineage.
title_full_unstemmed Comparative genomics search for losses of long-established genes on the human lineage.
title_sort comparative genomics search for losses of long-established genes on the human lineage.
publisher Public Library of Science (PLoS)
series PLoS Computational Biology
issn 1553-734X
1553-7358
publishDate 2007-12-01
description Taking advantage of the complete genome sequences of several mammals, we developed a novel method to detect losses of well-established genes in the human genome through syntenic mapping of gene structures between the human, mouse, and dog genomes. Unlike most previous genomic methods for pseudogene identification, this analysis is able to differentiate losses of well-established genes from pseudogenes formed shortly after segmental duplication or generated via retrotransposition. Therefore, it enables us to find genes that were inactivated long after their birth, which were likely to have evolved nonredundant biological functions before being inactivated. The method was used to look for gene losses along the human lineage during the approximately 75 million years (My) since the common ancestor of primates and rodents (the euarchontoglire crown group). We identified 26 losses of well-established genes in the human genome that were all lost at least 50 My after their birth. Many of them were previously characterized pseudogenes in the human genome, such as GULO and UOX. Our methodology is highly effective at identifying losses of single-copy genes of ancient origin, allowing us to find a few well-known pseudogenes in the human genome missed by previous high-throughput genome-wide studies. In addition to confirming previously known gene losses, we identified 16 previously uncharacterized human pseudogenes that are definitive losses of long-established genes. Among them is ACYL3, an ancient enzyme present in archaea, bacteria, and eukaryotes, but lost approximately 6 to 8 Mya in the ancestor of humans and chimps. Although losses of well-established genes do not equate to adaptive gene losses, they are a useful proxy to use when searching for such genetic changes. This is especially true for adaptive losses that occurred more than 250,000 years ago, since any genetic evidence of the selective sweep indicative of such an event has been erased.
url https://doi.org/10.1371/journal.pcbi.0030247
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