Néant I, Dubé F
Département d'Océanographie, Université du Québec à Rimouski, Québec, Canada.
Mol Reprod Dev. 1996 Aug;44(4):443-51. doi: 10.1002/(SICI)1098-2795(199608)44:4<443::AID-MRD3>3.0.CO;2-L.
6-dimethylaminopurine (6-DMAP), a potent protein kinase inhibitor, drives most cells into an interphasic stage. Experiments were undertaken with oocytes from three marine invertebrate species, i.e., Mytilus edulis, Spisula solidissima, and Strongylocentrotus droebachiensis, wherein oocytes were arrested at different phases of meiosis. 6-DMAP induced a continuous DNA synthesis in meiotic cells, whereas it allowed a single round of DNA replication in treated mitotic cells, regardless of species considered. The effects of 6-DMAP were accompanied in all cases by rephosphorylation on tyrosine of the p34cdc2 homolog, the M-phase promoting factor (MPF) catalytic subunit. The fact that 6-DMAP overcomes the inhibitory control of replication during meiosis suggests that this process depends upon protein phosphorylation, while DNA synthesis regulation in mitotic cells relies on 6-DMAP-insensitive events.
6-二甲基氨基嘌呤(6-DMAP)是一种有效的蛋白激酶抑制剂,可使大多数细胞进入间期阶段。实验使用了三种海洋无脊椎动物物种(即紫贻贝、硬壳蛤和球海胆)的卵母细胞,其中卵母细胞在减数分裂的不同阶段停滞。6-DMAP诱导减数分裂细胞中持续的DNA合成,而无论所考虑的物种如何,它都允许处理过的有丝分裂细胞进行一轮DNA复制。在所有情况下,6-DMAP的作用都伴随着p34cdc2同源物(M期促进因子(MPF)催化亚基)酪氨酸的重新磷酸化。6-DMAP克服减数分裂期间复制的抑制控制这一事实表明,该过程依赖于蛋白质磷酸化,而有丝分裂细胞中的DNA合成调节则依赖于对6-DMAP不敏感的事件。