Skip Navigation


MBE Advance Access originally published online on January 12, 2005
Molecular Biology and Evolution 2005 22(4):1044-1052; doi:10.1093/molbev/msi087
This Article
Right arrow Full Text Freely available
Right arrow FREE Full Text (PDF) Freely available
Right arrow Supplementary Material
Right arrow All Versions of this Article:
22/4/1044    most recent
msi087v1
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 (25)
Right arrowRequest Permissions
Google Scholar
Right arrow Articles by Good, J. M.
Right arrow Articles by Nachman, M. W.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Good, J. M.
Right arrow Articles by Nachman, M. W.
Social Bookmarking
 Add to CiteULike   Add to Connotea   Add to Del.icio.us  
What's this?

Molecular Biology and Evolution vol. 22 no. 4 © Society for Molecular Biology and Evolution 2005; all rights reserved.

Research Article

Rates of Protein Evolution Are Positively Correlated with Developmental Timing of Expression During Mouse Spermatogenesis

Jeffrey M. Good and Michael W. Nachman

Department of Ecology and Evolutionary Biology, University of Arizona

E-mail: jgood{at}email.arizona.edu.

Male reproductive genes often evolve very rapidly, and sexual selection is thought to be a primary force driving this divergence. We investigated the molecular evolution of 987 genes expressed at different times during mouse spermatogenesis to determine if the rate of evolution and the intensity of positive selection vary across stages of male gamete development. Using mouse-rat orthologs, we found that rates of protein evolution were positively correlated with the developmental timing of expression. Genes expressed early in spermatogenesis had rates of divergence similar to the genome median, while genes expressed after the onset of meiosis were found to evolve much more quickly. Rates of protein evolution were fastest for genes expressed during the dramatic morphogenesis of round spermatids into spermatozoa. Late-expressed genes were also more likely to be specific to the male germline. To test for evidence of positive selection, we analyzed the ratio of nonsynonymous to synonymous changes using a maximum likelihood framework in comparisons among mouse, rat, and human. Many genes showed evidence of positive selection, and most of these genes were expressed late in spermatogenesis and were testis specific. Overall, these data suggest that the intensity of positive selection associated with the evolution of male gametes varies considerably across development and acts primarily on phenotypes that develop late in spermatogenesis.

Key Words: Mus musculus • pleiotropy • sexual selection • sperm development • X chromosome


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
Mol Biol EvolHome page
H. Ramsay, L. H. Rieseberg, and K. Ritland
The Correlation of Evolutionary Rate with Pathway Position in Plant Terpenoid Biosynthesis
Mol. Biol. Evol., May 1, 2009; 26(5): 1045 - 1053.
[Abstract] [Full Text] [PDF]


Home page
Mol Biol EvolHome page
S. A. Ramm, L. McDonald, J. L. Hurst, R. J. Beynon, and P. Stockley
Comparative Proteomics Reveals Evidence for Evolutionary Diversification of Rodent Seminal Fluid and Its Functional Significance in Sperm Competition
Mol. Biol. Evol., January 1, 2009; 26(1): 189 - 198.
[Abstract] [Full Text] [PDF]


Home page
GeneticsHome page
L. M. Turner, E. B. Chuong, and H. E. Hoekstra
Comparative Analysis of Testis Protein Evolution in Rodents
Genetics, August 1, 2008; 179(4): 2075 - 2089.
[Abstract] [Full Text] [PDF]


Home page
GeneticsHome page
J. M. Good, M. D. Dean, and M. W. Nachman
A Complex Genetic Basis to X-Linked Hybrid Male Sterility Between Two Species of House Mice
Genetics, August 1, 2008; 179(4): 2213 - 2228.
[Abstract] [Full Text] [PDF]


Home page
GeneticsHome page
A. Llopart and J. M. Comeron
Recurrent Events of Positive Selection in Independent Drosophila Lineages at the Spermatogenesis Gene roughex
Genetics, June 1, 2008; 179(2): 1009 - 1020.
[Abstract] [Full Text] [PDF]


Home page
Mol Biol EvolHome page
M. D. Dean, J. M. Good, and M. W. Nachman
Adaptive Evolution of Proteins Secreted during Sperm Maturation: An Analysis of the Mouse Epididymal Transcriptome
Mol. Biol. Evol., February 1, 2008; 25(2): 383 - 392.
[Abstract] [Full Text] [PDF]


Home page
Mol Biol EvolHome page
S. A. Ramm, P. L. Oliver, C. P. Ponting, P. Stockley, and R. D. Emes
Sexual Selection and the Adaptive Evolution of Mammalian Ejaculate Proteins
Mol. Biol. Evol., January 1, 2008; 25(1): 207 - 219.
[Abstract] [Full Text] [PDF]


Home page
Genome ResHome page
C. Voolstra, D. Tautz, P. Farbrother, L. Eichinger, and B. Harr
Contrasting evolution of expression differences in the testis between species and subspecies of the house mouse
Genome Res., January 1, 2007; 17(1): 42 - 49.
[Abstract] [Full Text] [PDF]


Home page
GeneticsHome page
A. Oka, T. Aoto, Y. Totsuka, R. Takahashi, M. Ueda, A. Mita, N. Sakurai-Yamatani, H. Yamamoto, S. Kuriki, N. Takagi, et al.
Disruption of Genetic Interaction Between Two Autosomal Regions and the X Chromosome Causes Reproductive Isolation Between Mouse Strains Derived From Different Subspecies
Genetics, January 1, 2007; 175(1): 185 - 197.
[Abstract] [Full Text] [PDF]


Home page
GeneticsHome page
M. Metta, R. Gudavalli, J.-M. Gibert, and C. Schlotterer
No Accelerated Rate of Protein Evolution in Male-Biased Drosophila pseudoobscura Genes
Genetics, September 1, 2006; 174(1): 411 - 420.
[Abstract] [Full Text] [PDF]


Home page
GeneticsHome page
D. J. Begun, H. A. Lindfors, M. E. Thompson, and A. K. Holloway
Recently Evolved Genes Identified From Drosophila yakuba and D. erecta Accessory Gland Expressed Sequence Tags
Genetics, March 1, 2006; 172(3): 1675 - 1681.
[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]



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.