TY - JOUR
T1 - Evolutionary Quantitative Proteomics of Reproductive Protein Divergence in Drosophila
AU - Garlovsky, Martin D.
AU - Ahmed-Braimah, Yasir H.
N1 - Funding Information:
Acknowledgments—We thank Mike Deery, Yagnesh Umrania, and Renata Feret from the Cambridge Proteomics facility for technical assistance and James L. Hougland and Michelle A. Sieburg for use of a spectrophotometer. The Syracuse University HTC Campus Grid and the National Science Foundation award ACI-1341006 provided computing services. Members of the Center for Reproductive Evolution and Sean Stankowski provided helpful discussion and feedback about the project. The response from three anonymous reviewers improved the article. This work was supported by the National Institutes of Health grant R35GM147454 and Syracuse University. The content is solely the responsibility of the authors and does not necessarily represent the official views of the National Institutes of Health.
Funding Information:
We thank Mike Deery, Yagnesh Umrania, and Renata Feret from the Cambridge Proteomics facility for technical assistance and James L. Hougland and Michelle A. Sieburg for use of a spectrophotometer. The Syracuse University HTC Campus Grid and the National Science Foundation award ACI-1341006 provided computing services. Members of the Center for Reproductive Evolution and Sean Stankowski provided helpful discussion and feedback about the project. The response from three anonymous reviewers improved the article. This work was supported by the National Institutes of Health grant R35GM147454 and Syracuse University. The content is solely the responsibility of the authors and does not necessarily represent the official views of the National Institutes of Health.
Publisher Copyright:
© 2023 THE AUTHORS.
PY - 2023/8
Y1 - 2023/8
N2 - Reproductive traits often evolve rapidly between species. Understanding the causes and consequences of this rapid divergence requires characterization of female and male reproductive proteins and their effect on fertilization success. Species in the Drosophila virilis clade exhibit rampant interspecific reproductive incompatibilities, making them ideal for studies on diversification of reproductive proteins and their role in speciation. Importantly, the role of intraejaculate protein abundance and allocation in interspecific divergence is poorly understood. Here, we identify and quantify the transferred male ejaculate proteome using multiplexed isobaric labeling of the lower female reproductive tract before and immediately after mating using three species of the virilis group. We identified over 200 putative male ejaculate proteins, many of which show differential abundance between species, suggesting that males transfer a species-specific allocation of seminal fluid proteins during copulation. We also identified over 2000 female reproductive proteins, which contain female-specific serine-type endopeptidases that showed differential abundance between species and elevated rates of molecular evolution, similar to that of some male seminal fluid proteins. Our findings suggest that reproductive protein divergence can also manifest in terms of species-specific protein abundance patterns.
AB - Reproductive traits often evolve rapidly between species. Understanding the causes and consequences of this rapid divergence requires characterization of female and male reproductive proteins and their effect on fertilization success. Species in the Drosophila virilis clade exhibit rampant interspecific reproductive incompatibilities, making them ideal for studies on diversification of reproductive proteins and their role in speciation. Importantly, the role of intraejaculate protein abundance and allocation in interspecific divergence is poorly understood. Here, we identify and quantify the transferred male ejaculate proteome using multiplexed isobaric labeling of the lower female reproductive tract before and immediately after mating using three species of the virilis group. We identified over 200 putative male ejaculate proteins, many of which show differential abundance between species, suggesting that males transfer a species-specific allocation of seminal fluid proteins during copulation. We also identified over 2000 female reproductive proteins, which contain female-specific serine-type endopeptidases that showed differential abundance between species and elevated rates of molecular evolution, similar to that of some male seminal fluid proteins. Our findings suggest that reproductive protein divergence can also manifest in terms of species-specific protein abundance patterns.
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U2 - 10.1016/j.mcpro.2023.100610
DO - 10.1016/j.mcpro.2023.100610
M3 - Article
C2 - 37391044
AN - SCOPUS:85168795087
SN - 1535-9476
VL - 22
JO - Molecular and Cellular Proteomics
JF - Molecular and Cellular Proteomics
IS - 8
M1 - 100610
ER -