Coucouvanis E C, Jones P P
Department of Biological Sciences, Stanford University, CA 94305.
Mech Dev. 1993 Jul;42(1-2):49-58. doi: 10.1016/0925-4773(93)90097-h.
Primordial germ cells (PGCs) of the mouse undergo key developmental transitions during embryonic days 12-15. On day 12 they complete migration into the gonads. They cease mitotic proliferation on day 13 and subsequently enter sex-specific pathways of development. The molecular mechanisms controlling these transitions are poorly understood, yet they are crucial to production of normal gametes later in life. We have used the polymerase chain reaction (PCR) to directly compare levels of expression of several protooncogenes proposed to be involved in control of cell proliferation and differentiation in proliferating and differentiating PCGs of both sexes over a 4 day time course. We report here that mRNA levels for nuclear protooncogenes c-myc, c-fos, and c-jun increase dramatically in both sexes from little or no detectable expression on day 12 to high expression on days 13-15. We observe c-kit message on day 12 in combined PGCs of both sexes, in female but not male PGCs on day 13, and in both sexes on day 14, c-kit mRNA is undetectable on day 15 in either sex, c-mos is not expressed at detectable levels on day 12 in either sex, but increases gradually in female PGCs to very high levels on day 15. In male PGCs, c-mos is expressed at high levels on days 13-15. Our results are consistent with a role for protooncogenes c-myc, c-fos and c-jun in mediating the initial differentiation of PGCs of both sexes that occurs upon colonization of the gonad. Because c-kit and c-mos are expressed differentially in male and female day 13-15 germ cells, they may play roles in initiating or mediating progress along the sex-specific pathways of development that PGCs embark upon at this time.
小鼠的原始生殖细胞(PGCs)在胚胎第12至15天经历关键的发育转变。在第12天,它们完成向性腺的迁移。它们在第13天停止有丝分裂增殖,随后进入特定性别的发育途径。控制这些转变的分子机制尚不清楚,但它们对于后期正常配子的产生至关重要。我们使用聚合酶链反应(PCR)在4天的时间进程中直接比较了几种原癌基因在两性增殖和分化的PGCs中控制细胞增殖和分化的表达水平。我们在此报告,核原癌基因c-myc、c-fos和c-jun的mRNA水平在两性中均从第12天几乎检测不到表达急剧增加到第13至15天的高表达。我们在第12天的两性混合PGCs中观察到c-kit信息,在第13天的雌性而非雄性PGCs中观察到,在第14天的两性中均观察到,在第15天,无论雌雄,c-kit mRNA均检测不到,c-mos在第12天的两性中均未检测到可检测水平的表达,但在雌性PGCs中逐渐增加,在第15天达到非常高的水平。在雄性PGCs中,c-mos在第13至15天高水平表达。我们的结果与原癌基因c-myc、c-fos和c-jun在介导两性PGCs在性腺定植时发生的初始分化中的作用一致。因为c-kit和c-mos在第13至15天的雄性和雌性生殖细胞中差异表达,它们可能在启动或介导PGCs此时开始的特定性别发育途径的进展中发挥作用。