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Cellular genes derived from Gypsy/Ty3 retrotransposons in mammalian genomes

Authors :
Jean-Nicolas Volff
Institut de Génomique Fonctionnelle de Lyon (IGFL)
Université Claude Bernard Lyon 1 (UCBL)
Université de Lyon-Université de Lyon-Centre National de la Recherche Scientifique (CNRS)-Institut National de la Recherche Agronomique (INRA)-École normale supérieure - Lyon (ENS Lyon)
Association pour la Recherche contre le Cancer (ARC), Institut National de la Recherche Agronomique (INRA), Centre National de la Recherche Scientifique (CNRS), Ecole Nationale Superieure de Lyon (ENSL), Fondation pour la Recherche Medicale (FRM) et Agence Nationale de la Recherche (ANR)
École normale supérieure - Lyon (ENS Lyon)-Institut National de la Recherche Agronomique (INRA)-Université Claude Bernard Lyon 1 (UCBL)
Université de Lyon-Université de Lyon-Centre National de la Recherche Scientifique (CNRS)
École normale supérieure de Lyon (ENS de Lyon)-Institut National de la Recherche Agronomique (INRA)-Université Claude Bernard Lyon 1 (UCBL)
Source :
Annals of the New York Academy of Sciences, Conference on Natural Genetic Engineering and Natural Genome Editing, Conference on Natural Genetic Engineering and Natural Genome Editing, Jul 2008, Salzburg, Austria. pp.233-243, ⟨10.1111/j.1749-6632.2009.05005.x⟩
Publication Year :
2009

Abstract

International audience; Gypsy/Ty3 retrotransposons, a group of long terminal repeat retrotransposons related to vertebrate retroviruses, are found in the genome of many fungi, plants, and animals. Although multiple families of such retroelements are present in fish, active Gypsy/Ty3 retrotransposons have all been eliminated from the lineage leading to mammals at least 180 million years ago. However, over 50 cellular genes related to Gypsy/Ty3 retrotransposons have been identified in mammalian genomes, indicating recurrent "molecular domestication" of these elements by their host during evolution. Most retrotransposon-derived proteins are conserved in divergent mammalian species and show sequence similarity to Gag proteins, major structural proteins for retroelement particle formation. Among the proposed and demonstrated biological functions for gag-derived genes, placenta formation in the mouse requires two gag-derived genes from the same family. Some forms of epigenetic regulation of gag-related genes might derive from host genome defense mechanisms that repelled retrotransposon ancestors. Together, such observations support a major role for transposable elements as a source of new coding sequences allowing important genetic innovations during evolution.

Details

ISSN :
17496632
Volume :
1178
Database :
OpenAIRE
Journal :
Annals of the New York Academy of Sciences
Accession number :
edsair.doi.dedup.....fde978a05e87d16e338f7152ad157d47
Full Text :
https://doi.org/10.1111/j.1749-6632.2009.05005.x⟩