Skip Navigation

This Article
Right arrow Full Text Freely available
Right arrow FREE Full Text (PDF) Freely available
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 ISI Web of Science
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 arrow Search for citing articles in:
ISI Web of Science (19)
Right arrowRequest Permissions
Google Scholar
Right arrow Articles by Parsch, J.
Right arrow Articles by Hartl, D. L.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Parsch, J.
Right arrow Articles by Hartl, D. L.
Social Bookmarking
 Add to CiteULike   Add to Connotea   Add to Del.icio.us  
What's this?

Molecular Biology and Evolution 18:801-811 (2001)
© 2001 Society for Molecular Biology and Evolution


ARTICLE

Molecular Evolution of the ocnus and janus Genes in the Drosophila melanogaster Species Subgroup

John Parsch, Colin D. Meiklejohn, Elisabeth Hauschteck-Jungen, Peter Hunziker and Daniel L. Hartl

*Department of Organismic and Evolutionary Biology, Harvard University;
{dagger}Zoologisches Institut and
{ddagger}Biochemisches Institut, Universität Zürich, Zürich, Switzerland

Genes involved in male fertility are potential targets for sexual selection, and their evolution may play a role in reproductive isolation and speciation. Here we describe a new Drosophila melanogaster gene, ocnus (ocn), that encodes a protein abundant in testes nuclear extracts. RT-PCR indicates that ocn transcription is limited to males and is specific to testes. ocn shares homology with another testis-specific gene, janusB (janB), and is located just distal to janB on chromosome 3. The two genes also share homology with the adjacent janusA (janA) gene, suggesting that multiple duplication events have occurred within this region of the genome. We cloned and sequenced these three genes from species of the D. melanogaster species subgroup. Phylogenetic analysis based on protein-encoding sequences predicts a duplication pattern of janA -> janA janB -> janA janB ocn, with the latter event occurring after the divergence of the D. melanogaster and Drosophila obscura species groups. We found significant heterogeneity in the rates of evolution among the three genes within the D. melanogaster species subgroup as measured by the ratio of nonsynonymous to synonymous substitutions, suggesting that diversification of gene function followed each duplication event and that each gene evolved under different selective constraints. All three genes showed faster rates of evolution than genes encoding proteins with metabolic function. These results are consistent with previous studies that have detected an increased rate of evolution in genes with reproductive function.


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


This article has been cited by other articles:


Home page
Proc. Natl. Acad. Sci. USAHome page
L. M. Mikhaylova, A. M. Boutanaev, and D. I. Nurminsky
Transcriptional regulation by Modulo integrates meiosis and spermatid differentiation in male germ line
PNAS, August 8, 2006; 103(32): 11975 - 11980.
[Abstract] [Full Text] [PDF]


Home page
GeneticsHome page
B. J. Wagstaff and D. J. Begun
Molecular Population Genetics of Accessory Gland Protein Genes and Testis-Expressed Genes in Drosophila mojavensis and D. arizonae
Genetics, November 1, 2005; 171(3): 1083 - 1101.
[Abstract] [Full Text] [PDF]


Home page
Mol Biol EvolHome page
E. S. Balakirev, V. R. Chechetkin, V. V. Lobzin, and F. J. Ayala
Entropy and GC Content in the {beta}-esterase Gene Cluster of the Drosophila melanogaster Subgroup
Mol. Biol. Evol., October 1, 2005; 22(10): 2063 - 2072.
[Abstract] [Full Text] [PDF]


Home page
Mol Biol EvolHome page
Z. Zhang, T. M. Hambuch, and J. Parsch
Molecular Evolution of Sex-Biased Genes in Drosophila
Mol. Biol. Evol., November 1, 2004; 21(11): 2130 - 2139.
[Abstract] [Full Text] [PDF]


Home page
GeneticsHome page
C. D. Meiklejohn, Y. Kim, D. L. Hartl, and J. Parsch
Identification of a Locus Under Complex Positive Selection in Drosophila simulans by Haplotype Mapping and Composite-Likelihood Estimation
Genetics, September 1, 2004; 168(1): 265 - 279.
[Abstract] [Full Text] [PDF]


Home page
GeneticsHome page
J. Parsch
Selective Constraints on Intron Evolution in Drosophila
Genetics, December 1, 2003; 165(4): 1843 - 1851.
[Abstract] [Full Text] [PDF]


Home page
Proc. Natl. Acad. Sci. USAHome page
C. D. Meiklejohn, J. Parsch, J. M. Ranz, and D. L. Hartl
Rapid evolution of male-biased gene expression in Drosophila
PNAS, August 19, 2003; 100(17): 9894 - 9899.
[Abstract] [Full Text] [PDF]


Home page
Mol Biol EvolHome page
C. I. Castillo-Davis and D. L. Hartl
Genome Evolution and Developmental Constraint in Caenorhabditis elegans
Mol. Biol. Evol., May 1, 2002; 19(5): 728 - 735.
[Abstract] [Full Text] [PDF]


Home page
GeneticsHome page
J. Parsch, C. D. Meiklejohn, and D. L. Hartl
Patterns of DNA Sequence Variation Suggest the Recent Action of Positive Selection in the janus-ocnus Region of Drosophila simulans
Genetics, October 1, 2001; 159(2): 647 - 657.
[Abstract] [Full Text] [PDF]



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.