Sinka Rita, Jankovics Ferenc, Somogyi Kálmán, Szlanka Tamás, Lukácsovich Tamás, Erdélyi Miklós
Institute of Genetics, Biological Research Center of the Hungarian Academy of Sciences, H-6701 PO Box 521, Szeged, Hungary.
Development. 2002 Jul;129(14):3469-78. doi: 10.1242/dev.129.14.3469.
Embryonic germ cell formation and abdomen development in Drosophila requires localisation and site specific translation of oskar mRNA in the posterior part of the oocyte. Targeting of oskar function to the posterior pole of the oocyte needs a large set of proteins and RNAs, encoded by posterior group genes. Consequently, mutations in the posterior group genes can result in embryos without abdomens and/or germ cells. During a systematic hobo-mediated mutant isolation screen, we identified poirot, a novel posterior group gene, owing to its germ cell-less phenotype. We show that the lack of poirot activity dramatically decreases OSK protein levels, without affecting the oskar mRNA distribution. In poirot mutant oocytes, delocalised OSK protein is observed, indicating that wild-type poirot has a role in the anchoring process of the OSK protein at the posterior pole. Furthermore, we demonstrate that poirot acts in an isoform-specific manner, only the short OSK isoform is affected, while the long OSK isoform remains at wild-type levels in poirot mutants.
果蝇中胚胎生殖细胞的形成和腹部发育需要osk mRNA在卵母细胞后部的定位和位点特异性翻译。将osk功能靶向到卵母细胞的后极需要大量由后部组基因编码的蛋白质和RNA。因此,后部组基因的突变会导致胚胎没有腹部和/或生殖细胞。在一项系统性的由hobo介导的突变体分离筛选中,我们鉴定出了一个新的后部组基因——poirot,这是由于其无生殖细胞的表型。我们发现,缺乏poirot活性会显著降低OSK蛋白水平,而不影响osk mRNA的分布。在poirot突变体卵母细胞中,观察到OSK蛋白发生了异位,这表明野生型poirot在OSK蛋白于后极的锚定过程中发挥作用。此外,我们证明poirot以一种异构体特异性的方式发挥作用,只有短OSK异构体受到影响,而长OSK异构体在poirot突变体中保持野生型水平。