Tian M, Maniatis T
Harvard University, Department of Biochemistry and Molecular Biology, Cambridge, Massachusetts 02138.
Cell. 1993 Jul 16;74(1):105-14. doi: 10.1016/0092-8674(93)90298-5.
Female-specific splicing of Drosophila doublesex (dsx) pre-mRNA is regulated by the products of the transformer (tra) and transformer 2 (tra2) genes. In this paper we show that Tra and Tra2 act by recruiting general splicing factors to a regulatory element located downstream of a female-specific 3' splice site. Remarkably, Tra, Tra2, and members of the serine/arginine-rich (SR) family of general splicing factors are sufficient to commit dsx pre-mRNA to female-specific splicing, and individual SR proteins differ significantly in their ability to participate in commitment complex formation. Characterization of the proteins associated with affinity-purified complex formed on dsx pre-mRNA reveals the presence of Tra, Tra2, SR proteins, and additional unidentified components. We conclude that Tra, Tra2, and SR proteins are essential components of a splicing enhancer complex.
果蝇双性基因(dsx)前体mRNA的雌性特异性剪接受转变蛋白(tra)和转变蛋白2(tra2)基因产物的调控。在本文中,我们表明Tra和Tra2通过将一般剪接因子招募到位于雌性特异性3'剪接位点下游的调控元件上发挥作用。值得注意的是,Tra、Tra2以及富含丝氨酸/精氨酸(SR)的一般剪接因子家族成员足以使dsx前体mRNA进行雌性特异性剪接,并且单个SR蛋白在参与形成起始复合物的能力上存在显著差异。对与dsx前体mRNA上亲和纯化复合物相关的蛋白质进行表征,揭示了Tra、Tra2、SR蛋白以及其他未鉴定成分的存在。我们得出结论,Tra、Tra2和SR蛋白是剪接增强子复合物的重要组成部分。