Mount S M
Department of Microbiology, University of Maryland, College Park, USA.
Bioessays. 1997 Mar;19(3):189-92. doi: 10.1002/bies.950190302.
SR proteins are essential for the splicing of messenger RNA precursors in vitro, where they also alter splice site selection in a concentration-dependent manner. Although experiments involving overexpression or dominant mutations have confirmed that these proteins can influence RNA processing decisions in vivo, similar results with loss-of-function mutations have been lacking. Now, a system for genetic depletion of the chicken B cell line DT40 has revealed that the SR protein ASF/SF2 (alternative splicing factor/splicing factor 2) is essential for viability in these cells(1). This study opens the way for a complete functional dissection of this protein, and other SR proteins, in vivo.
SR蛋白对于体外信使RNA前体的剪接至关重要,在体外它们还以浓度依赖的方式改变剪接位点的选择。尽管涉及过表达或显性突变的实验已证实这些蛋白可在体内影响RNA加工决策,但功能缺失突变的类似结果却一直缺乏。现在,一种用于鸡B细胞系DT40基因敲除的系统表明,SR蛋白ASF/SF2(可变剪接因子/剪接因子2)对于这些细胞的存活至关重要(1)。这项研究为在体内对该蛋白及其他SR蛋白进行完整的功能剖析开辟了道路。