Ross A, Munger S, Capel B
Department of Cell Biology, Duke University Medical Center, Durham, NC 27710, USA.
Sex Dev. 2007;1(2):127-37. doi: 10.1159/000100034.
Relatively little is known regarding the signals that regulate the proliferation and sex-specific development of germ cells during mammalian fetal gonad differentiation. Members of the bone morphogenetic protein (BMP) family have been identified as key regulators of germ cells in the Drosophila gonad. Here we show that in mice Bmp7 is expressed in gonads of both sexes and is required for germ cell proliferation during a narrow window of development between 10.5-11.5 days post coitum (dpc). The proliferation defect is more severe in male than in female embryos suggesting that there are sexually dimorphic compensatory pathways. BMP signaling appears to be an evolutionarily conserved pathway regulating embryonic germ cell proliferation in vertebrate and invertebrate species.
关于在哺乳动物胎儿性腺分化过程中调节生殖细胞增殖和性别特异性发育的信号,人们了解相对较少。骨形态发生蛋白(BMP)家族成员已被确定为果蝇性腺中生殖细胞的关键调节因子。在此我们表明,在小鼠中,Bmp7在两性性腺中均有表达,并且在交配后10.5 - 11.5天(dpc)这一狭窄的发育窗口期内对生殖细胞增殖是必需的。雄性胚胎中的增殖缺陷比雌性胚胎更严重,这表明存在性别二态性的补偿途径。BMP信号似乎是一条在脊椎动物和无脊椎动物物种中调节胚胎生殖细胞增殖的进化保守途径。