Parent genes of retrotransposition-generated gene duplicates in Drosophila melanogaster have distinct expression profiles

Morgan G.I. Langille, Denise V. Clark

Résultat de recherche: Articleexamen par les pairs

9 Citations (Scopus)

Résumé

Genes arising by retrotransposition are always different from their parent genes from the outset. In addition, the cDNA must insert into a region that allows expression or it will become a processed pseudogene. We sought to determine whether this class of gene duplication differs from other gene duplications based on functional criteria. Using amino acid sequences from Drosophila melanogaster, we identified retroduplicated gene pairs at various levels of sequence identity. Analysis of gene ontology annotations showed some enrichment of retroduplications in the cellular physiological processes class. Retroduplications show a higher level of nucleotide substitution than other gene duplications, suggesting a higher rate of divergence. Remarkably, analysis of microarray data for gene expression during embryogenesis showed that parent genes are more highly expressed relative to their retroduplicated copies, tandem duplications, and all genes. Furthermore, an expressed sequence tag library representation shows a broader distribution for parent genes than for all other genes and, as found previously by others, retroduplicated gene transcripts are found most abundantly in testes. Therefore, in examining retroduplicated gene pairs, we have found that parent genes of retroduplications are also a distinctive class in terms of transcript expression levels and distribution.

Langue d'origineEnglish
Pages (de-à)334-343
Nombre de pages10
JournalGenomics
Volume90
Numéro de publication3
DOI
Statut de publicationPublished - sept. 2007
Publié à l'externeOui

Note bibliographique

Funding Information:
We thank the Canadian Bioinformatics Resource at the National Research Council in Halifax, Canada, for computing support. This work was supported by a Natural Sciences and Engineering Research Council of Canada grant to D.V.C.

ASJC Scopus Subject Areas

  • Genetics

PubMed: MeSH publication types

  • Journal Article
  • Research Support, Non-U.S. Gov't

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