Bell L R, Maine E M, Schedl P, Cline T W
Department of Biology, Princeton University, New Jersey 08544.
Cell. 1988 Dec 23;55(6):1037-46. doi: 10.1016/0092-8674(88)90248-6.
The switch gene, Sex-lethal (Sxl), controls sexual development and dosage compensation. It must be active in females and inactive in males throughout development. Analysis of Sxl cDNAs shows that this on/off regulation may be explained by differential RNA splicing; only female transcripts appear to encode functional products, whereas all male transcripts contain an exon that truncates the open reading frame. The functional female product shows sequence similarities with ribonucleoproteins, suggesting that it is an RNA binding protein. Thus, we propose that Sxl encodes a factor that interacts with both its own pre-mRNA (accounting for positive autoregulation) and that of downstream genes to confer female-specific splicing. In this way, a single, simple mechanism could account for both the maintenance and expression of the sexually determined state.
性别致死基因(Sex-lethal,Sxl)控制着性别发育和剂量补偿。在整个发育过程中,它在雌性中必须处于激活状态,而在雄性中处于失活状态。对Sxl cDNA的分析表明,这种开/关调节可能是由不同的RNA剪接来解释的;只有雌性转录本似乎编码功能性产物,而所有雄性转录本都包含一个外显子,该外显子会截断开放阅读框。功能性的雌性产物与核糖核蛋白具有序列相似性,这表明它是一种RNA结合蛋白。因此,我们提出Sxl编码一种因子,该因子与其自身的前体mRNA(负责正向自调节)以及下游基因的前体mRNA相互作用,以赋予雌性特异性剪接。通过这种方式,一个单一、简单的机制就可以解释性别决定状态的维持和表达。