Chapman T, Neubaum D M, Wolfner M F, Partridge L
Department of Biology, University College London, UK.
Proc Biol Sci. 2000 Jun 7;267(1448):1097-105. doi: 10.1098/rspb.2000.1114.
A crucial factor determining sperm fertilization success in multiply mated Drosophila melanogaster females is the efficiency with which sperm are stored. This process is modulated by the accessory gland protein Acp36DE. In this study, we show that the effect of Acp36DE on sperm storage itself alters the outcome of sperm competition. As second-mating males, Acp36DE1 (null) males had significantly lower P2-values than Acp36DE2 (truncation) or Acp36DE+ (control) males, as might be expected as the null males' sperm are poorly stored. We used spermless males, which are null for Acp36DE, to show that, in the absence of sperm co-transfer, Acp36DE itself could not displace first-male sperm. The results therefore suggest that males null for Acp36DE suffer in sperm displacement because fewer sperm are stored or retained, not because Acp36DE itself displaces sperm. Acp36DE1 (null) males also gained significantly fewer fertilizations than controls when they were the first males to mate. Using spermless males, we also showed that significantly more second-male offspring were produced following the transfer of Acp36DE by spermless first-mating males. This implies that the transfer of Acp36DE itself by the first male facilitated the storage or use of the second male's sperm and that co-transfer with sperm is not necessary for Acp36DE effects on second-male sperm storage. Acp36DE may persist in the reproductive tract and aid the storage of any sperm including those of later-mating males or prime the female for future efficient sperm storage. Our results indicate that mutations in genes that affect sperm storage can drastically affect the outcome of sperm competition.
在多次交配的黑腹果蝇雌性中,决定精子受精成功的一个关键因素是精子储存的效率。这个过程受到附属腺蛋白Acp36DE的调节。在本研究中,我们表明Acp36DE对精子储存本身的影响改变了精子竞争的结果。作为第二次交配的雄性,Acp36DE1(无效)雄性的P2值显著低于Acp36DE2(截短)或Acp36DE+(对照)雄性,正如预期的那样,因为无效雄性的精子储存不佳。我们使用了对Acp36DE无效的无精子雄性,以表明在没有精子共同转移的情况下,Acp36DE本身无法取代首次交配雄性的精子。因此,结果表明,Acp36DE无效的雄性在精子取代方面表现不佳,是因为储存或保留的精子较少,而不是因为Acp36DE本身取代了精子。当Acp36DE1(无效)雄性作为首次交配的雄性时,它们获得的受精也显著少于对照组。使用无精子雄性,我们还表明,无精子的首次交配雄性转移Acp36DE后,产生的第二次交配雄性后代显著更多。这意味着首次交配雄性转移Acp36DE本身促进了第二次交配雄性精子的储存或使用,并且Acp36DE对第二次交配雄性精子储存的影响并不需要与精子共同转移。Acp36DE可能会在生殖道中持续存在,并有助于储存任何精子,包括后来交配雄性的精子,或者使雌性为未来高效的精子储存做好准备。我们的结果表明,影响精子储存的基因突变会极大地影响精子竞争的结果。