Maezawa Takanobu, Arita Kayo, Shigenobu Shuji, Kobayashi Satoru
Okazaki Institute for Integrative Bioscience, National Institute for Basic Biology, National Institutes of Natural Sciences, Higashiyama, Myodaiji, Okazaki, Japan.
Dev Growth Differ. 2009 May;51(4):453-61. doi: 10.1111/j.1440-169X.2009.01108.x.
Nanos (Nos) is an evolutionarily conserved protein essential for the maintenance of primordial germ cells (PGCs). In Drosophila, the PGCs or pole cells express head involution defective (hid), which is required for caspase activation, but its translation is repressed by maternal Nos. In the absence of Nos activity, translation of hid mRNA into protein induces apoptosis in pole cells. However, it remains unclear how hid mRNA is regulated in pole cells. Here, we report that hid expression requires eiger (egr), a tumor necrosis factor ligand (TNF) homologue, which is induced in pole cells by decapentaplegic (dpp). In addition, we demonstrate that p53 and loki (lok), a damage-activated kinase known to be required for p53 phosphorylation, are both required for hid expression in pole cells. Since maternal lok mRNA is enriched in pole cells, it is possible that ubiquitously distributed p53 is activated in pole cells by maternal Lok. We propose that hid expression is activated in a pole cell-specific manner by loki/p53 and dpp/egr during embryogenesis.
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(PGC)的维持至关重要。在果蝇中,PGC或极细胞表达头部内卷缺陷蛋白(hid),这是半胱天冬酶激活所必需的,但其翻译受到母体Nos的抑制。在没有Nos活性的情况下,hid mRNA翻译成蛋白质会诱导极细胞凋亡。然而,目前尚不清楚hid mRNA在极细胞中是如何被调控的。在此,我们报告hid的表达需要艾格蛋白(egr),一种肿瘤坏死因子配体(TNF)同源物,它由果蝇的骨形态发生蛋白(dpp)在极细胞中诱导产生。此外,我们证明p53和洛基蛋白(lok),一种已知p53磷酸化所必需的损伤激活激酶,在极细胞中hid的表达中都是必需的。由于母体lok mRNA在极细胞中富集,有可能广泛分布的p53在极细胞中被母体Lok激活。我们提出,在胚胎发育过程中,hid的表达通过洛基蛋白/ p53和dpp / egr以极细胞特异性的方式被激活。