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Seminal fluid plays an essential role in promoting male reproductive success and modulating female physiology and behavior. In the fruit fly, <i>Drosophila melanogaster</i>, Sex Peptide (SP) is the best-characterized protein mediator of these effects. It is secreted from the paired male accessory glands (AGs), which, like the mammalian prostate and seminal vesicles, generate most of the seminal fluid contents. After mating, SP binds to spermatozoa and is retained in the female sperm storage organs. It is gradually released by proteolytic cleavage and induces several long-term postmating responses, including increased ovulation, elevated feeding, and reduced receptivity to remating, primarily signaling through the SP receptor (SPR). Here, we demonstrate a previously unsuspected SPR-independent function for SP. We show that, in the AG lumen, SP and secreted proteins with membrane-binding anchors are carried on abundant, large neutral lipid-containing microcarriers, also found in other SP-expressing <i>Drosophila</i> species. These microcarriers are transferred to females during mating where they rapidly disassemble. Remarkably, SP is a key microcarrier assembly and disassembly factor. Its absence leads to major changes in the seminal proteome transferred to females upon mating. Males expressing nonfunctional SP mutant proteins that affect SP's binding to and release from sperm in females also do not produce normal microcarriers, suggesting that this male-specific defect contributes to the resulting widespread abnormalities in ejaculate function. Our data therefore reveal a role for SP in formation of seminal macromolecular assemblies, which may explain the presence of SP in <i>Drosophila</i> species that lack the signaling functions seen in <i>D</i> <i>melanogaster</i>.

Original publication

DOI

10.1073/pnas.2019622118

Type

Journal article

Journal

Proceedings of the National Academy of Sciences of the United States of America

Publication Date

02/2021

Volume

118

Addresses

Department of Physiology, Anatomy and Genetics, University of Oxford, OX1 3QX Oxford, United Kingdom.