Schwer B, Shuman S
Department of Biochemistry, Robert Wood Johnson Medical School, Piscataway, New Jersey 08854, USA.
RNA. 1996 Jun;2(6):574-83.
Acquisition of the 5'cap is the earliest modification event during eukaryotic mRNA synthesis. The cap is thought to facilitate later processing steps, such as pre-mRNA splicing. If this is so, then a defect in cap synthesis should impact on splicing in vivo. We tested this hypothesis by examining the consequences of conditional inactivation of the Saccharomyces cerevisiae CEG1 gene, which encodes mRNA guanylyltransferase (capping enzyme). Two different ceg1-ts mutants, Y66A and C354Y, displayed a pre-mRNA processing (prp) defect, characterized by an increase in the amount of unspliced pre-mRNA after shift to nonpermissive temperature and a decrease in the amount of mature mRNA. The guanylyltransferase activities of the Y66A and C354Y proteins were thermolabile, suggesting that defective capping in vivo was contributory to the prp phenotype. Although these results provide the first genetic link between capping and splicing in vivo, we were unable to demonstrate a role for either the cap or the capping enzyme during yeast pre-mRNA splicing in vitro.
5'帽的获得是真核生物mRNA合成过程中最早发生的修饰事件。人们认为帽子结构有助于后续的加工步骤,比如前体mRNA剪接。如果真是这样,那么帽合成缺陷应该会在体内影响剪接。我们通过检测酿酒酵母CEG1基因条件性失活的后果来验证这一假设,该基因编码mRNA鸟苷酸转移酶(加帽酶)。两种不同的ceg1-ts突变体Y66A和C354Y表现出前体mRNA加工(prp)缺陷,其特征是转移到非允许温度后未剪接前体mRNA的量增加,而成熟mRNA的量减少。Y66A和C354Y蛋白的鸟苷酸转移酶活性对温度敏感,这表明体内加帽缺陷是导致prp表型的原因。尽管这些结果提供了体内加帽与剪接之间的首个遗传联系,但我们无法在体外酵母前体mRNA剪接过程中证明帽或加帽酶的作用。