Variation in sex peptide expression in D. melanogaster

Genetics Research

Volumn 91, Issue 4, 2009, Pages 237-242

  Smith, D T ^a   Hosken, D J ^a   Ffrench Constant, R H ^a   Wedell, N ^a  

^a UNIVERSITY OF EXETER   (United Kingdom)

Author keywords

[No Author keywords available]

Indexed keywords

DROSOPHILA PROTEIN; RNA; SEX PEPTIDE; UNCLASSIFIED DRUG;

ARTICLE; COPULATION; DROSOPHILA MELANOGASTER; FEMALE; GENE DISRUPTION; GENETIC ASSOCIATION; GENETIC SELECTION; GENETIC VARIABILITY; MALE; NONHUMAN; PROTEIN EXPRESSION; SEX DIFFERENCE; WOLBACHIA;

ANIMALS; DROSOPHILA MELANOGASTER; DROSOPHILA PROTEINS; FEMALE; GENE EXPRESSION PROFILING; GENETIC VARIATION; HOST-PATHOGEN INTERACTIONS; MALE; PEPTIDES; REGRESSION ANALYSIS; REVERSE TRANSCRIPTASE POLYMERASE CHAIN REACTION; SEXUAL BEHAVIOR, ANIMAL; SPECIES SPECIFICITY; WOLBACHIA;

DROSOPHILA MELANOGASTER; WOLBACHIA;

EID: 70349248413     PISSN: 00166723     EISSN: 14695073     Source Type: Journal    
DOI: 10.1017/S0016672309000226     Document Type: Article

References (59)

1. Aigaki, T., Fleischmann, I., Chen, P. S. & Kubli, E. (1991). Ectopic expression of sex peptide alters reproductive behavior of female D. melanogaster. Neuron 7, 557-563.
2. Baker, D. A., Meadows, L. A., Wang, J., Dow, J. A. & Russell, S. (2007). Variable sexually dimorphic gene expression in laboratory strains of Drosophila melanogaster. BMC Genomics 8, 10.
3. Begun, D. J. & Lindfors, H. A. (2005). Rapid evolution of genomic Acp complement in the melanogaster subgroup of Drosophila. Molecular Biology and Evolution 22, 2010-2021.
4. Bertram, M. J., Neubaum, D. M. & Wolfner, M. F. (1996). Localization of the Drosophila male accessory gland protein Acp36DE in the mated female suggests a role in sperm storage. Insect Biochemistry and Molecular Biology 26, 971-980.
5. Champion de Crespigny, F. E. C., Pitt, T. D. & Wedell, N. (2006). Increased male mating rate in Drosophila is associated with Wolbachia infection. Journal of Evolutionary Biology 19, 1964-1972.
6. Champion de Crespigny, F. E. C. & Wedell, N. (2006). Wolbachia infection reduces sperm competitive ability in an insect. Proceedings of the Royal Society B-Biological Sciences 273, 1455-1458.
7. Chapman, T., Bangham, J., Vinti, G., Seifried, B., Lung, O., Wolfner, M. F., Smith, H. K. & Partridge, L. (2003). The sex peptide of Drosophila melanogaster: Female postmating responses analyzed by using RNA interference. Proceedings of the National Academy of Sciences of the USA 100, 9923-9928.
8. Chapman, T., Herndon, L. A., Heifetz, Y., Partridge, L. & Wolfner, M. F. (2001). The Acp26Aa seminal fluid protein is a modulator of early egg hatchability in Drosophila melanogaster. Proceedings of the Royal Society of London Series B-Biological Sciences 268, 1647-1654.
9. Chapman, T., Liddle, L. F., Kalb, J. M., Wolfner, M. F. & Partridge, L. (1995). Cost of mating in Drosophila melanogaster females is mediated by male accessory-gland products. Nature 373, 241-244.
10. Chen, P. S., Stummzollinger, E., Aigaki, T., Balmer, J., Bienz, M. & Bohlen, P. (1988). A male accessory-gland peptide that regulates reproductive behavior of female Drosophila melanogaster. Cell 54, 291-298.
11. Cirera, S. & Aguade, M. (1997). Evolutionary history of the sex-peptide (Acp70A) gene region in Drosophila melanogaster. Genetics 147 189-197.
12. Coleman, S., Drahn, B., Petersen, G., Stolorov, J. & Kraus, K. (1995). A Drosophila male accessory gland protein that is a member of the serpin superfamily of proteinase inhibitors is transferred to females during mating. Insect Biochemistry and Molecular Biology 25, 203-207.
13. Corby-Harris, V., Pontaroli, A. C., Shimkets, L. J., Bennetzen, J. L., Habel, K. E. & Promislow, D. E. L. (2007). Geographical distribution and diversity of bacteria associated with natural populations of Drosophila melanogaster. Applied and Environmental Microbiology 73 3470-3479.
14. Dobson, S. L., Bourtzis, K., Braig, H. R., Jones, B. F., Zhou, W. G., Rousset, F. & O'Neill, S. L. (1999). Wolbachia infections are distributed throughout insect somatic and germ line tissues. Insect Biochemistry and Molecular Biology 29, 153-160.
15. Eberhard, W. G. (1996). Female Control: Sexual Selection by Cryptic Female Choice. Princeton, NJ: Princeton University Press.
16. Findlay, G. D., Yi, X. H., MacCoss, M. J. & Swanson, W. J. (2008). Proteomics reveals novel Drosophila seminal fluid proteins transferred at mating. PLoS Biology 6, 1417-1426.
17. Fiumera, A. C., Dumont, B. L. & Clark, A. G. (2005). Sperm competitive ability in Drosophila melanogaster associated with variation in male reproductive proteins. Genetics 169, 243-257.
18. Fiumera, A. C., Dumont, B. L. & Clark, A. G. (2007). Associations between sperm competition and natural variation in male reproductive genes on the third chromosome of Drosophila melanogaster. Genetics 176, 1245-1260.
19. Folstad, I. & Karter, A. J. (1992). Parasites, bright males, and the immunocompetence handicap. American Naturalist 139, 603-622.
20. Gromko, M. H., Gilbert, D. G. & Richmond, R. C. (1984a). Sperm transfer and use in the multiple mating system of Drosophila. In Sperm Competition and the Evolution of Animal Mating Systems (ed. R. L. Smith), pp. 372-427. San Diego: Academic Press, Inc.
21. Gromko, M. H., Newport, M. E. A. & Kortier, M. G. (1984b). Sperm dependence of female receptivity to remating in Drosophila melanogaster. Evolution 38, 1273-1282.
22. Haerty, W., Jagadeeshan, S., Kulathinal, R. J., Wong, A., Ram, K. R., Sirot, L. K., Levesque, L., Artieri, C. G., Wolfner, M. F., Civetta, A. & Singh, R. S. (2007). Evolution in the fast lane: Rapidly evolving sex-related genes in Drosophila. Genetics 177, 1321-1335.
23. Harshman, L. G. & Zera, A. J. (2007). The cost of reproduction: The devil in the details. Trends in Ecology & Evolution 22, 80-86.
24. Heifetz, Y., Lung, O., Frongillo, E. A. & Wolfner, M. F. (2000). The Drosophila seminal fluid protein Acp26Aa stimulates release of oocytes by the ovary. Current Biology 10, 99-102.
25. Heifetz, Y., Vandenberg, L. N., Cohn, H. I. & Wolfner, M. F. (2005). Two cleavage products of the Drosophila accessory gland protein ovulin can independently induce ovulation. Proceedings of the National Academy of Sciences of the USA 102, 743-748.
26. Herndon, L. A. & Wolfner, M. F. (1995). A Drosophila seminal fluid protein, Acp26Aa, stimulates egg-laying in females for 1 day after mating. Proceedings of the National Academy of Sciences of the USA 92, 10114-10118.
27. Hihara, F. (1981). Effects of the male accessory gland secretion on oviposition and remating in females of Drosophila melanogaster. Zoological Magazine 90, 307-316.
28. Hoffmann, A. A., Clancy, D. J. & Merton, E. (1994). Cytoplasmic incompatibility in Australian populations of Drosophila melanogaster. Genetics 136, 993-999.
29. Hoffmann, A. A., Turelli, M. & Harshman, L. G. (1990). Factors affecting the distribution of cytoplasmic incompatibility in Drosophila simulans. Genetics 126, 933-948.
30. Jeyaprakash, A. & Hoy, M. A. (2000). Long PCR improves Wolbachia DNA amplification: wsp sequences found in 76% of sixty-three arthropod species. Insect Molecular Biology 9, 393-405.
31. Linklater, J. R., Wertheim, B., Wigby, S. & Chapman, T. (2007). Ejaculate depletion patterns evolve in response to experimental manipulation of sex ratio in Drosophila melanogaster. Evolution 61, 2027-2034.
32. Livak, K. J. & Schmittgen, T. D. (2001). Analysis of relative gene expression data using real-time quantitative PCR and the 2(T)(-Delta Delta C) method. Methods 25, 402-408.
33. McGraw, E. A., Merritt, D. J., Droller, J. N. & O'Neill, S. L. (2002). Wolbachia density and virulence attenuation after transfer into a novel host. Proceedings of the National Academy of Sciences of the USA 99, 2918-2923.
34. Min, K. T. & Benzer, S. (1997). Wolbachia, normally a symbiont of Drosophila, can be virulent, causing degeneration and early death. Proceedings of the National Academy of Sciences of the USA 94 10792-10796.
35. Monsma, S. A., Harada, H. A. & Wolfner, M. F. (1990). Synthesis of two Drosophila male accessory gland proteins and their fate after transfer to the female during mating. Developmental Biology 142 465-475.
36. Moshitzky, P., Fleischmann, I., Chaimov, N., Saudan, P., Klauser, S., Kubli, E. & Applebaum, S. W. (1996). Sex-peptide activates juvenile hormone biosynthesis in the Drosophila melanogaster corpus allatum. Archives of Insect Biochemistry and Physiology 32, 363-374.
37. Mueller, J. L., Ram, K. R., McGraw, L. A., Qazi, M. C. B., Siggia, E. D., Clark, A. G., Aquadro, C. F. & Wolfner, M. F. (2005). Cross-species comparison of Drosophila male accessory gland protein genes. Genetics 171, 131-143.
38. Negri, I., Franchini, A., Mandrioli, M., Mazzoglio, P. J. & Almai, A. (2008). The gonads of Zyginidia pullula males feminized by Wolbachia pipientis. Bulletin of Insectology 61, 213-214.
39. Neubaum, D. M. & Wolfner, M. F. (1999). Mated Drosophila melanogaster females require a seminal fluid protein, Acp36DE, to store sperm efficiently. Genetics 153, 845-857.
40. Ottiger, M., Soller, M., Stocker, R. F. & Kubli, E. (2000). Binding sites of Drosophila melanogaster sex peptide pheromones. Journal of Neurobiology 44, 57-71.
41. Peng, J., Chen, S., Busser, S., Liu, H. F., Honegger, T. & Kubli, E. (2005). Gradual release of sperm bound sex-peptide controls female postmating behavior in Drosophila. Current Biology 15, 207-213.
42. Pfaffl, M. W. (2001). A new mathematical model for relative quantification in real-time RT-PCR. Nucleic Acids Research 29 6.
43. Ram, K. R., Ji, S. & Wolfner, M. F. (2005). Fates and targets of male accessory gland proteins in mated female Drosophila melanogaster. Insect Biochemistry and Molecular Biology 35, 1059-1071.
44. Ram, K. R. & Wolfner, M. F. (2007). Seminal influences: Drosophila Acps and the molecular interplay between males and females during reproduction. Integrative and Comparative Biology 47, 427-445.
45. Rogers, D. W., Chapman, T., Fowler, K. & Pomiankowski, A. (2005). Mating-induced reduction in accessory reproductive organ size in the stalk-eyed fly Cyrtodiopsis dalmanni. BMC Evolutionary Biology 5, 6.
46. Rowe, L. & Houle, D. (1996). The lek paradox and the capture of genetic variance by condition dependent traits. Proceedings of the Royal Society of London Series B-Biological Sciences 263, 1415-1421.
47. Schully, S. D. & Hellberg, M. E. (2006). Positive selection on nucleotide substitutions and indels in accessory gland proteins of the Drosophila pseudoobscura subgroup. Journal of Molecular Evolution 62, 793-802.
48. Snook, R. R., Cleland, S. Y., Wolfner, M. F. & Karr, T. L. (2000). Offsetting effects of Wolbachia infection and heat shock on sperm production in Drosophila simulans: Analyses of fecundity, fertility and accessory gland proteins. Genetics 155, 167-178.
49. Snook, R. R. & Hosken, D. J. (2004). Sperm death and dumping in Drosophila. Nature 428, 939-941.
50. Swanson, W. J., Clark, A. G., Waldrip-Dail, H. M., Wolfner, M. F. & Aquadro, C. F. (2001). Evolutionary EST analysis identifies rapidly evolving male reproductive proteins in Drosophila. Proceedings of the National Academy of Sciences of the USA 98, 7375-7379.
51. Swanson, W. J. & Vacquier, V. D. (2002). The rapid evolution of reproductive proteins. Nature Reviews Genetics 3, 137-144.
52. Tram, U., Ferree, P. A. & Sullivan, W. (2003). Identification of Wolbachia-host interacting factors through cytological analysis. Microbes and Infection 5, 999-1011.
53. Tram, U. & Sullivan, W. (2002). Role of delayed nuclear envelope breakdown and mitosis in Wolbachia-induced cytoplasmic incompatibility. Science 296, 1124-1126.
54. Weeks, A. R., Turelli, M., Harcombe, W. R., Reynolds, K. T. & Hoffmann, A. A. (2007). From parasite to mutualist: Rapid evolution of Wolbachia in natural populations of Drosophila. PLoS Biology 5, 997-1005.
55. Werren, J. H. (1997). Biology of Wolbachia. Annual Review of Entomology 42, 587-609.
56. Werren, J. H., Zhang, W. & Guo, L. R. (1995). Evolution and phylogeny of Wolbachia- reproductive parasites of arthropods. Proceedings of the Royal Society of London Series B-Biological Sciences 261, 55-63.
57. Wigby, S. & Chapman, T. (2005). Sex peptide causes mating costs in female Drosophila melanogaster. Current Biology 15, 316-321.
58. Wolfner, M. F. (2002). The gifts that keep on giving: Physiological functions and evolutionary dynamics of male seminal proteins in Drosophila. Heredity 88, 85-93.
59. Yapici, N., Kim, Y. J., Ribeiro, C. & Dickson, B. J. (2008). A receptor that mediates the post-mating switch in Drosophila reproductive behaviour. Nature 451, 33-31.