Sato Kimihiro, Hayashi Yoshiki, Ninomiya Yuichi, Shigenobu Shuji, Arita Kayo, Mukai Masanori, Kobayashi Satoru
Okazaki Institute for Integrative Bioscience, National Institute for Basic Biology, National Institutes of Natural Sciences, Higashiyama, Myodaiji, Okazaki 444-8787, Japan.
Proc Natl Acad Sci U S A. 2007 May 1;104(18):7455-60. doi: 10.1073/pnas.0610052104. Epub 2007 Apr 20.
Nanos (Nos) is an evolutionarily conserved protein essential for the survival of primordial germ cells. In Drosophila, maternal Nos partitions into pole cells and suppresses apoptosis to permit proper germ-line development. However, how this critical event is regulated by Nos has remained elusive. Here, we report that Nos represses apoptosis of pole cells by suppressing translation of head involution defective (hid), a member of the RHG gene family that is required for Caspase activation. In addition, we demonstrate that hid acts in concert with another RHG gene, sickle (skl), to induce apoptosis. Expression of skl is induced in pole cells by maternal tao-1, a ste20-like serine/threonine kinase. Tao-1-dependent skl expression is required to potentiate hid activity. However, skl expression is largely suppressed in normal pole cells. Once the pole cells lack maternal Nos, Tao-1-dependent skl expression is fully activated, suggesting that skl expression is also restricted by Nos. These findings provide the first evidence that the germ line is maintained through the regulated expression of RHG genes.
纳米蛋白(Nos)是一种在进化上保守的蛋白质,对原始生殖细胞的存活至关重要。在果蝇中,母体Nos进入极细胞并抑制细胞凋亡,以确保生殖系的正常发育。然而,Nos如何调控这一关键事件仍不清楚。在这里,我们报告Nos通过抑制头部内卷缺陷蛋白(hid)的翻译来抑制极细胞的凋亡,hid是半胱天冬酶激活所需的RHG基因家族的成员。此外,我们证明hid与另一个RHG基因镰刀蛋白(skl)协同作用诱导细胞凋亡。母体tao-1(一种类Ste20丝氨酸/苏氨酸激酶)在极细胞中诱导skl的表达。Tao-1依赖的skl表达是增强hid活性所必需的。然而,skl在正常极细胞中的表达受到很大抑制。一旦极细胞缺乏母体Nos,Tao-1依赖的skl表达就会被完全激活,这表明skl的表达也受到Nos的限制。这些发现首次证明生殖系是通过RHG基因的调控表达来维持的。