4.7 Article

The Old and the New: Discovery Proteomics Identifies Putative Novel Seminal Fluid Proteins in Drosophila

期刊

MOLECULAR & CELLULAR PROTEOMICS
卷 18, 期 3, 页码 S23-S33

出版社

AMER SOC BIOCHEMISTRY MOLECULAR BIOLOGY INC
DOI: 10.1074/mcp.RA118.001098

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资金

  1. NSF [DEB-0093149]
  2. NERC [NE/N013832/1, NE/B504065/1, NE/I014632/1]
  3. EU [ITN-2008-213780 SPECIATION]
  4. University of Sheffield Biological Mass Spectrophotometry Facility (Yorkshire Cancer Research) [Shend01]
  5. University of Sheffield Biological Mass Spectrophotometry Facility (Wellcome Trust)
  6. Leverhulme Early Career Fellowship [ECF-2015-453]
  7. Kyoto Institute of Technology
  8. Natural Environment Research Council [NE/P000592/1, NE/B504065/1, NE/I014632/1, NE/N013832/1] Funding Source: researchfish

向作者/读者索取更多资源

Seminal fluid proteins (SFPs), the nonsperm component of male ejaculates produced by male accessory glands, are viewed as central mediators of reproductive fitness. SFPs effect both male and female post-mating functions and show molecular signatures of rapid adaptive evolution. Although Drosophila melanogaster is the dominant insect model for understanding SFP evolution, understanding of SFP evolutionary causes and consequences require additional comparative analyses of close and distantly related taxa. Although SFP identification was historically challenging, advances in label-free quantitative proteomics expands the scope of studying other systems to further advance the field. Focused studies of SFPs has so far overlooked the proteomes of male reproductive glands and their inherent complex protein networks for which there is little information on the overall signals of molecular evolution. Here we applied label-free quantitative proteomics to identify the accessory gland proteome and secretome in Drosophila pseudoobscura, a close relative of D. melanogaster, and use the dataset to identify both known and putative novel SFPs. Using this approach, we identified 163 putative SFPs, 32% of which overlapped with previously identified D. melanogaster SFPs and show that SFPs with known extracellular annotation evolve more rapidly than other proteins produced by or contained within the accessory gland. Our results will further the understanding of the evolution of SFPs and the underlying male accessory gland proteins that mediate reproductive fitness of the sexes.

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