Pronounced Postmating Response in the Drosophila Female Reproductive Tract Fluid Proteome.


Journal

Molecular & cellular proteomics : MCP
ISSN: 1535-9484
Titre abrégé: Mol Cell Proteomics
Pays: United States
ID NLM: 101125647

Informations de publication

Date de publication:
2021
Historique:
received: 11 04 2021
revised: 09 09 2021
accepted: 21 09 2021
pubmed: 2 10 2021
medline: 25 3 2022
entrez: 1 10 2021
Statut: ppublish

Résumé

Fertility depends on the progression of complex and coordinated postmating processes within the extracellular environment of the female reproductive tract (FRT). Molecular interactions between ejaculate and FRT proteins regulate many of these processes, including sperm motility, migration, storage, and modification, along with concurrent changes in the female. Although extensive progress has been made in the proteomic characterization of the male-derived components of sperm and seminal fluid, investigations into the FRT have remained more limited. To achieve a comparable level of knowledge regarding female-derived proteins that comprise the reproductive environment, we utilized semiquantitative MS-based proteomics to study the composition of the FRT tissue and, separately, the luminal fluid, before and after mating in Drosophila melanogaster. Our approach leveraged whole-fly isotopic labeling to delineate female proteins from transferred male ejaculate proteins. Our results revealed several characteristics that distinguish the FRT fluid proteome from the FRT tissue proteome: (1) the fluid proteome is encoded by genes with higher overall levels of FRT gene expression and tissue specificity, including many genes with enriched expression in the fat body, (2) fluid-biased proteins are enriched for metabolic functions, and (3) the fluid exhibits pronounced postmating compositional changes. The dynamic mating-induced proteomic changes in the FRT fluid inform our understanding of secretory mechanisms of the FRT, serve as a foundation for establishing female contributions to the ejaculate-female interactions that regulate fertility, and highlight the importance of applying proteomic approaches to characterize the composition and dynamics of the FRT environment.

Identifiants

pubmed: 34597791
pii: S1535-9476(21)00128-6
doi: 10.1016/j.mcpro.2021.100156
pmc: PMC9357439
pii:
doi:

Substances chimiques

Drosophila Proteins 0
Proteome 0

Types de publication

Journal Article Research Support, N.I.H., Extramural Research Support, U.S. Gov't, Non-P.H.S.

Langues

eng

Sous-ensembles de citation

IM

Pagination

100156

Subventions

Organisme : NICHD NIH HHS
ID : R21 HD088910
Pays : United States

Informations de copyright

Copyright © 2021 The Authors. Published by Elsevier Inc. All rights reserved.

Déclaration de conflit d'intérêts

Conflict of interest The authors declare no competing interests.

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Auteurs

Caitlin E McDonough-Goldstein (CE)

Center for Reproductive Evolution, Department of Biology, Syracuse University, Syracuse, New York, USA. Electronic address: mcdonouce@gmail.com.

Emma Whittington (E)

Center for Reproductive Evolution, Department of Biology, Syracuse University, Syracuse, New York, USA.

Erin L McCullough (EL)

Center for Reproductive Evolution, Department of Biology, Syracuse University, Syracuse, New York, USA.

Sharleen M Buel (SM)

Center for Reproductive Evolution, Department of Biology, Syracuse University, Syracuse, New York, USA.

Scott Erdman (S)

Department of Biology, Syracuse University, Syracuse, New York, USA.

Scott Pitnick (S)

Center for Reproductive Evolution, Department of Biology, Syracuse University, Syracuse, New York, USA.

Steve Dorus (S)

Center for Reproductive Evolution, Department of Biology, Syracuse University, Syracuse, New York, USA. Electronic address: sdorus@syr.edu.

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