Lynch K W, Maniatis T
Department of Molecular and Cellular Biology, Harvard University, Cambridge, Massachusetts 02138.
Genes Dev. 1995 Feb 1;9(3):284-93. doi: 10.1101/gad.9.3.284.
Regulated alternative splicing of doublesex (dsx) pre-mRNA requires a splicing enhancer designated the dsx repeat element (dsxRE) that contains six copies of a 13-nucleotide repeat sequence. Previous studies have shown that the activity of the dsxRE requires the splicing regulators Transformer (Tra) and Transformer 2 (Tra2), and one or more members of the SR family of general splicing factors. In this paper we identify a purine-rich enhancer (PRE) sequence within the dsxRE, and show that this element functionally synergizes with the repeat sequences. In vitro binding studies show that the PRE is required for specific binding of Tra2 to the dsxRE, and that Tra and SR proteins bind cooperatively to the dsxRE in the presence or absence of the PRE. Thus positive control of dsx pre-mRNA splicing requires the Tra- and Tra2-dependent assembly of a multiprotein complex on at least two distinct enhancer elements.
双性基因(doublesex,dsx)前体mRNA的可变剪接受一个名为dsx重复元件(dsxRE)的剪接增强子调控,该元件包含六个13个核苷酸重复序列的拷贝。先前的研究表明,dsxRE的活性需要剪接调节因子Transformer(Tra)和Transformer 2(Tra2),以及一般剪接因子SR家族的一个或多个成员。在本文中,我们在dsxRE内鉴定出一个富含嘌呤的增强子(PRE)序列,并表明该元件与重复序列在功能上协同作用。体外结合研究表明,PRE是Tra2与dsxRE特异性结合所必需的,并且在有或没有PRE的情况下,Tra和SR蛋白协同结合到dsxRE上。因此,dsx前体mRNA剪接的正调控需要在至少两个不同的增强子元件上由Tra和Tra2依赖组装的多蛋白复合物。