Liu Y, Belote J M
Department of Biology, Syracuse University, NY 13244, USA.
Mol Gen Genet. 1995 Jul 28;248(2):182-9. doi: 10.1007/BF02190799.
Sex determination in Drosophila melanogaster is initiated in the early embryo by a signal provided by three types of genes: (1) X-linked numerator elements [e.g., sisterless-a (sis-a) and sisterless-b (sis-b)], (2) autosomally linked denominator elements [e.g., deadpan (dpn)], and (3) maternal factors [e.g., daughterless (da)]. This signal acts to stimulate transcription from an embryo-specific promoter of the master regulatory gene Sex-lethal (Sxl) in embryos that have two X chromosomes (females), while it fails to activate Sxl in those with only one X (males). It has been previously proposed that competitive dimerizations among the components of this signal might provide the molecular basis for this sex specificity. Here, we use the yeast two-hybrid system to demonstrate specific protein-protein interactions among the above-mentioned factors, and to delimit their interacting domains. These results support and extend the model of the molecular basis of the X/A ratio signal.
(1)X连锁的分子元件[如无姐妹a(sis-a)和无姐妹b(sis-b)],(2)常染色体连锁的分母元件[如呆板(dpn)],以及(3)母体因子[如无女儿(da)]。该信号在具有两条X染色体的胚胎(雌性)中刺激主调控基因性致死(Sxl)的胚胎特异性启动子转录,而在只有一条X染色体的胚胎(雄性)中则无法激活Sxl。此前有人提出,该信号成分之间的竞争性二聚化可能为这种性别特异性提供分子基础。在这里,我们使用酵母双杂交系统来证明上述因子之间的特异性蛋白质-蛋白质相互作用,并界定它们的相互作用结构域。这些结果支持并扩展了X/A比率信号分子基础的模型。