Skip Navigation


MBE Advance Access originally published online on October 14, 2008
Molecular Biology and Evolution 2009 26(1):61-70; doi:10.1093/molbev/msn227
This Article
Right arrow Full Text
Right arrow Full Text (PDF)
Right arrow Supplementary Data
Right arrow All Versions of this Article:
26/1/61    most recent
msn227v1
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Add to My Personal Archive
Right arrow Download to citation manager
Right arrowRequest Permissions
Google Scholar
Right arrow Articles by Aguadé, M.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Aguadé, M.
Social Bookmarking
 Add to CiteULike   Add to Connotea   Add to Del.icio.us  
What's this?

© The Author 2008. Published by Oxford University Press on behalf of the Society for Molecular Biology and Evolution. All rights reserved. For permissions, please e-mail: journals.permissions@oxfordjournals.org

Research Articles

Nucleotide and Copy-Number Polymorphism at the Odorant Receptor Genes Or22a and Or22b in Drosophila melanogaster

Montserrat Aguadé

Departament de Genètica, Facultat de Biologia, Universitat de Barcelona, Barcelona, Spain

E-mail: maguade{at}ub.edu.

Accepted for publication September 27, 2008.

In Drosophila, odorant receptors are encoded by an old and moderately sized multigene family. Or22a and Or22b are two tandemly arranged genes of this family that have proved to be the result of a rather young duplication. Nucleotide variation in the region spanning both duplicates was surveyed in four natural populations (two African and two non-African) of Drosophila melanogaster and also analyzed in species of the melanogaster subgroup. The intraspecific survey revealed a particular copy-number polymorphism in some of the studied populations, with the two genes (Or22a and Or22b) present in the long variant and a single chimeric gene (Or22ab) present in the short variant. Estimated nucleotide diversity was higher in the short than in the long variant, despite the ancestral character of the latter variant in D. melanogaster. The general skew toward low-frequency variants detected in the non-African long variant and its reduced level of silent polymorphism relative to divergence is consistent with the recent fixation of an advantageous mutation at, or nearby, the Or22 long variant region. The nonnegligible frequency of the short variant and the presence of a highly divergent haplotype in the East African sample would point to direct or indirect selection for its maintenance in the species. There was evidence for a generally more rapid evolution of the Or22b copy at both synonymous and nonsynonymous sites. However, an excess of nonsynonymous substitutions was only detected in the early history of this copy.

Key Words: Drosophila melanogaster • nucleotide polymorphism • odorant receptors


Michael Nachman, Associate Editor


Add to CiteULike CiteULike   Add to Connotea Connotea   Add to Del.icio.us Del.icio.us    What's this?




Disclaimer: Please note that abstracts for content published before 1996 were created through digital scanning and may therefore not exactly replicate the text of the original print issues. All efforts have been made to ensure accuracy, but the Publisher will not be held responsible for any remaining inaccuracies. If you require any further clarification, please contact our Customer Services Department.