Institut for Integrative Biology of the Cell (I2BC), CNRS, Université Paris-Sud, CEA, Gif-sur-Yvette, France.
Laboratoire Evolution, Génomes, Comportements, Ecologie (EGCE), CNRS, IRD, Université Paris-Saclay, Gif-sur-Yvette, France.
PLoS Genet. 2024 Mar 14;20(3):e1011186. doi: 10.1371/journal.pgen.1011186. eCollection 2024 Mar.
Egg activation, representing the critical oocyte-to-embryo transition, provokes meiosis completion, modification of the vitelline membrane to prevent polyspermy, and translation of maternally provided mRNAs. This transition is triggered by a calcium signal induced by spermatozoon fertilization in most animal species, but not in insects. In Drosophila melanogaster, mature oocytes remain arrested at metaphase-I of meiosis and the calcium-dependent activation occurs while the oocyte moves through the genital tract. Here, we discovered that the oenocytes of fruitfly females are required for egg activation. Oenocytes, cells specialized in lipid-metabolism, are located beneath the abdominal cuticle. In adult flies, they synthesize the fatty acids (FAs) that are the precursors of cuticular hydrocarbons (CHCs), including pheromones. The oenocyte-targeted knockdown of a set of FA-anabolic enzymes, involved in very-long-chain fatty acid (VLCFA) synthesis, leads to a defect in egg activation. Given that some but not all of the identified enzymes are required for CHC/pheromone biogenesis, this putative VLCFA-dependent remote control may rely on an as-yet unidentified CHC or may function in parallel to CHC biogenesis. Additionally, we discovered that the most posterior ventral oenocyte cluster is in close proximity to the uterus. Since oocytes dissected from females deficient in this FA-anabolic pathway can be activated in vitro, this regulatory loop likely operates upstream of the calcium trigger. To our knowledge, our findings provide the first evidence that a physiological extra-genital signal remotely controls egg activation. Moreover, our study highlights a potential metabolic link between pheromone-mediated partner recognition and egg activation.
卵激活代表了卵子到胚胎的关键转变,引发了减数分裂的完成、卵黄膜的修饰以防止多精入卵,以及母体提供的 mRNA 的翻译。在大多数动物物种中,这个转变是由精子受精引发的钙信号触发的,但昆虫中并非如此。在黑腹果蝇中,成熟的卵母细胞在减数分裂的中期 I 停滞,而钙依赖性的激活发生在卵母细胞通过生殖道移动时。在这里,我们发现果蝇雌性的脂肪体细胞对于卵激活是必需的。脂肪体细胞专门从事脂质代谢,位于腹部表皮下面。在成年果蝇中,它们合成脂肪酸(FAs),这些脂肪酸是表皮烃(CHCs)的前体,包括信息素。脂肪体细胞靶向敲低一组参与非常长链脂肪酸(VLCFA)合成的 FA 合成酶,导致卵激活缺陷。鉴于一些但不是所有鉴定出的酶都参与 CHC/信息素生物合成,这种推测的 VLCFA 依赖的远程控制可能依赖于尚未鉴定的 CHC,或者与 CHC 生物合成平行发挥作用。此外,我们发现最尾侧的腹侧脂肪细胞簇与子宫非常接近。由于从缺乏这种 FA 合成途径的雌性中分离的卵母细胞可以在体外被激活,因此这个调节环可能在钙触发之前起作用。据我们所知,我们的发现提供了第一个证据,证明了一个生理上的非生殖信号可以远程控制卵激活。此外,我们的研究强调了信息素介导的伴侣识别和卵激活之间的潜在代谢联系。