Sorbonne Université, CNRS, Laboratoire de Biologie du Développement - Institut de Biologie Paris Seine, LBD - IBPS, F-75005 Paris, France.
Sorbonne Université, CNRS, Laboratoire de Biologie du Développement de Villefranche-sur-mer (LBDV), 06230 Villefranche-sur-mer, France.
Cells. 2020 May 7;9(5):1150. doi: 10.3390/cells9051150.
During oocyte development, meiosis arrests in prophase of the first division for a remarkably prolonged period firstly during oocyte growth, and then when awaiting the appropriate hormonal signals for egg release. This prophase arrest is finally unlocked when locally produced maturation initiation hormones (MIHs) trigger entry into M-phase. Here, we assess the current knowledge of the successive cellular and molecular mechanisms responsible for keeping meiotic progression on hold. We focus on two model organisms, the amphibian , and the hydrozoan jellyfish Conserved mechanisms govern the initial meiotic programme of the oocyte prior to oocyte growth and also, much later, the onset of mitotic divisions, via activation of two key kinase systems: Cdk1-Cyclin B/Gwl (MPF) for M-phase activation and Mos-MAPkinase to orchestrate polar body formation and cytostatic (CSF) arrest. In contrast, maintenance of the prophase state of the fully-grown oocyte is assured by highly specific mechanisms, reflecting enormous variation between species in MIHs, MIH receptors and their immediate downstream signalling response. Convergence of multiple signalling pathway components to promote MPF activation in some oocytes, including , is likely a heritage of the complex evolutionary history of spawning regulation, but also helps ensure a robust and reliable mechanism for gamete production.
在卵母细胞发育过程中,减数分裂首先在第一次分裂的前期停滞很长一段时间,首先在卵母细胞生长期间,然后在等待卵子释放的适当激素信号时。当局部产生的成熟起始激素 (MIH) 触发进入 M 期时,这种前期停滞最终被解除。在这里,我们评估了负责维持减数分裂进展的连续细胞和分子机制的最新知识。我们专注于两种模式生物,两栖类和水螅水母。保守的机制在卵母细胞生长之前以及稍后的有丝分裂分裂开始时,通过激活两个关键的激酶系统,来控制卵母细胞的初始减数分裂程序:用于 M 期激活的 Cdk1-Cyclin B/Gwl (MPF) 和 Mos-MAP 激酶来协调极体形成和细胞静止 (CSF) 停滞。相比之下,完全生长的卵母细胞的前期状态由高度特异性机制来保证,这反映了 MIH、MIH 受体及其直接下游信号转导反应在物种之间存在巨大差异。多种信号通路成分的汇聚以促进一些卵母细胞中的 MPF 激活,包括 ,这可能是产卵调节复杂进化历史的遗产,但也有助于确保配子产生的稳健可靠机制。