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PMID: 17196768 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't

Frequent emergence and functional resurrection of processed pseudogenes in the human and mouse genomes.

Gene ·Vol. 389 ·No. 2 ·2007-03-15 ·Pages 196-203

Sakai H, Koyanagi KO, Imanishi T, Itoh T, Gojobori T

Abstract

Despite the wide distribution of processed pseudogenes in mammalian genomes, such as those of human and mouse, relatively little is known about their roles in genomic evolution. While gene duplications are recognized as one of the major driving forces in genome evolution, processed pseudogenes, which are retrotransposed copies of mRNAs, have been regarded as junk or selfish DNA for a long time. In order to elucidate the quantitative and qualitative contribution of processed pseudogenes to the mammalian genome evolution, we attempted to detect processed pseudogenes by extensively mapping the mRNAs to both the human and mouse genomes, and then we estimated the rate of their emergence. As a result, we revealed that the rate of pseudogene emergence was about 1-2% per gene per million years, which was as high as the rate (0.9%) of gene duplication in the human genome, although the rate of pseudogene emergence was found to drastically decrease in the hominid lineage. Furthermore, 1% of the processed pseudogenes seemed to be reinvigorated by post-retrotransposition transcription, many of them preserving the intact coding regions. Since the expression patterns of transcribed pseudogenes in various tissues were quite different between human and mouse, their emergence might have led to species-specific evolution. Our results indicate that the generation of processed pseudogenes was not wholly futile but instead has been an indispensable resource, driving dynamic evolution of the mammalian genomes.

MeSH Terms
Amino Acid Sequence Animals Evolution, Molecular Genome Genome, Human Humans Mice Molecular Sequence Data Phylogeny Pseudogenes RNA, Messenger/genetics,metabolism Sequence Alignment Transcription, Genetic
Chemicals
RNA, Messenger
Authors & Affiliations
5 authors, click to expand affiliations / ORCID
Sakai Hiroaki
Japan Biological Information Research Center, Japan Biological Informatics Consortium, AIST Bio-IT Research Bldg 7F, 2-42 Aomi, Tokyo, Japan.
Koyanagi Kanako O
Imanishi Tadashi
Itoh Takeshi
Gojobori Takashi
Article Info
Journal
Gene
Abbr.
Gene
ISSN
0378-1119
Published
2007-03-15
Epub
2006-00-18
Pages
196-203
Language
English
Region
Netherlands
NLM ID
7706761
Subset
IM
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