Sakamoto H, Inoue K, Higuchi I, Ono Y, Shimura Y
Department of Biophysics, Faculty of Science, Kyoto University, Japan.
Nucleic Acids Res. 1992 Nov 11;20(21):5533-40. doi: 10.1093/nar/20.21.5533.
Drosophila melanogaster somatic sexual differentiation is accomplished by serial function of the products of sex-determination genes. Sex-lethal (Sxl), is one such gene. It is functionally expressed only in female flies. The sex-specific expression of this gene is regulated by alternative mRNA splicing which results in either the inclusion or exclusion of the translation stop codon containing third exon. Although previous genetic and molecular analyses suggest that functional Sxl expression is maintained by a positive feedback loop, where the female-specific Sxl product promotes the synthesis of its own female-specific mRNA, the mechanistic details of such regulation have remained unclear. We have developed a cotransfection system using Drosophila cultured (Kc) cells in which Sxl primary transcripts are expressed with or without the female specific Sxl product. Here we show that the female-specific Sxl product induces the synthesis of its own female-specific mRNA by negative control of male-specific splicing. Deletion, substitution, and binding experiments have demonstrated that multiple uridine-rich sequences in the introns around the male-specific third exon are involved in the splicing regulation of Sxl pre-mRNA.
果蝇的体细胞性别分化是由性别决定基因产物的系列功能完成的。性致死基因(Sxl)就是这样一个基因。它仅在雌蝇中功能性表达。该基因的性别特异性表达受可变mRNA剪接调控,可变mRNA剪接导致包含第三个外显子的翻译终止密码子被包含或排除。尽管先前的遗传学和分子分析表明功能性Sxl表达通过正反馈环维持,其中雌性特异性Sxl产物促进其自身雌性特异性mRNA的合成,但这种调控的机制细节仍不清楚。我们利用果蝇培养的(Kc)细胞开发了一种共转染系统,在该系统中,Sxl初级转录本在有或没有雌性特异性Sxl产物的情况下表达。在这里我们表明,雌性特异性Sxl产物通过对雄性特异性剪接的负调控诱导其自身雌性特异性mRNA的合成。缺失、取代和结合实验表明,雄性特异性第三个外显子周围内含子中的多个富含尿苷的序列参与了Sxl前体mRNA的剪接调控。