Martin J R, Raibaud A, Ollo R
Institut Pasteur, Laboratoire de Biologie Moléculaire de la Drosophile, Paris, France.
Nature. 1994 Feb 24;367(6465):741-5. doi: 10.1038/367741a0.
The genes torso (tor) and torso-like (tsl) are two of the Drosophila maternal group genes implicated in a receptor tyrosine kinase signalling pathway that specifies terminal cell fate (reviewed in ref. 3). Loss-of-function mutations in these loci cause an identical phenotype in which pattern elements from the anterior (acron) and posterior (telson) ends have been deleted. We have cloned the tsl gene and demonstrate here that, in agreement with previous genetic data, it encodes a protein that is secreted and whose transcription is restricted to specialized categories of follicle cells localized at the poles of the egg chamber. At early blastoderm stage, tsl protein forms a symmetrical concentration gradient at the poles on the surface of the devitellinized embryo. Unrestricted expression of the tsl protein in tsl female mutants induces terminal pattern elements and suppresses the formation of abdomen in embryos. These results suggest that the tsl protein is the ligand that binds to the torso receptor.
躯干基因(tor)和类躯干基因(tsl)是果蝇母体基因中的两个,它们参与了决定末端细胞命运的受体酪氨酸激酶信号通路(参考文献3中有综述)。这些基因座的功能丧失突变会导致相同的表型,即前(顶节)后(尾节)两端的模式元件缺失。我们克隆了tsl基因,并在此证明,与先前的遗传数据一致,它编码一种分泌蛋白,其转录仅限于位于卵室两极的特定类型的卵泡细胞。在胚盘早期,tsl蛋白在脱卵黄胚胎表面的两极形成对称的浓度梯度。tsl雌性突变体中tsl蛋白的无限制表达会诱导末端模式元件的形成,并抑制胚胎中腹部的形成。这些结果表明,tsl蛋白是与躯干受体结合的配体。