Sureau A, Gattoni R, Dooghe Y, Stévenin J, Soret J
CNRS-UMR 146, Institut Curie, Bât. 110, Centre Universitaire, 91405 Orsay, France.
EMBO J. 2001 Apr 2;20(7):1785-96. doi: 10.1093/emboj/20.7.1785.
SC35 belongs to the family of SR proteins that regulate alternative splicing in a concentration-dependent manner in vitro and in vivo. We previously reported that SC35 is expressed through alternatively spliced mRNAs with differing 3' untranslated sequences and stabilities. Here, we show that overexpression of SC35 in HeLa cells results in a significant decrease of endogenous SC35 mRNA levels along with changes in the relative abundance of SC35 alternatively spliced mRNAs. Remarkably, SC35 leads to both an exon inclusion and an intron excision in the 3' untranslated region of its mRNAs. In vitro splicing experiments performed with recombinant SR proteins demonstrate that SC35, but not ASF/SF2 or 9G8, specifically activates these alternative splicing events. Interestingly, the resulting mRNA is very unstable and we present evidence that mRNA surveillance is likely to be involved in this instability. SC35 therefore constitutes the first example of a splicing factor that controls its own expression through activation of splicing events leading to expression of unstable mRNA.
SC35属于SR蛋白家族,该家族在体外和体内以浓度依赖的方式调节可变剪接。我们之前报道过,SC35通过具有不同3'非翻译序列和稳定性的可变剪接mRNA进行表达。在此,我们表明,在HeLa细胞中过表达SC35会导致内源性SC35 mRNA水平显著下降,同时SC35可变剪接mRNA的相对丰度也会发生变化。值得注意的是,SC35会导致其mRNA的3'非翻译区出现外显子包含和内含子切除。用重组SR蛋白进行的体外剪接实验表明,是SC35而非ASF/SF2或9G8特异性激活了这些可变剪接事件。有趣的是,产生的mRNA非常不稳定,我们提供的证据表明,mRNA监测可能与这种不稳定性有关。因此,SC35构成了一个剪接因子的首个例子,该剪接因子通过激活剪接事件来控制自身表达,从而导致不稳定mRNA的表达。