Weng Y, Czaplinski K, Peltz S W
Department of Molecular Genetics and Microbiology, Robert Wood Johnson Medical School, University of Medicine and Dentistry of New Jersey, Piscataway 08854, USA.
Mol Cell Biol. 1996 Oct;16(10):5477-90. doi: 10.1128/MCB.16.10.5477.
mRNA degradation is an important control point in the regulation of gene expression and has been linked to the process of translation. One clear example of this linkage is the nonsense-mediated mRNA decay pathway, in which nonsense mutations in a gene can reduce the abundance of the mRNA transcribed from that gene. For the yeast Saccharomyces cerevisiae, the Upf1 protein (Upf1p), which contains a cysteine- and histidine-rich region and nucleoside triphosphate hydrolysis and helicase motifs, was shown to be a trans-acting factor in this decay pathway. Biochemical analysis of the wild-type Upf1p demonstrates that it has RNA-dependent ATPase, RNA helicase, and RNA binding activities. A UPF1 gene disruption results in stabilization of nonsense-containing mRNAs, leading to the production of enough functional product to overcome an auxotrophy resulting from a nonsense mutation. A genetic and biochemical study of the UPF1 gene was undertaken in order to understand the mechanism of Upf1p function in the nonsense-mediated mRNA decay pathway. Our analysis suggests that Upf1p is a multifunctional protein with separable activities that can affect mRNA turnover and nonsense suppression. Mutations in the conserved helicase motifs of Upf1p that inactivate its mRNA decay function while not allowing suppression of leu2-2 and tyr7-1 nonsense alleles have been identified. In particular, one mutation located in the ATP binding and hydrolysis motif of Upf1p that changed the aspartic and glutamic acid residues to alanine residues (DE572AA) lacked ATPase and helicase activities, and the mutant formed a Upf1p:RNA complex in the absence of ATP; surprisingly, however, the Upf1p:RNA complex dissociated as a consequence of ATP binding. This result suggests that ATP binding, independent of its hydrolysis, can modulate Upf1p:RNA complex formation for this mutant protein. The role of the RNA binding activity of Upf1p in modulating nonsense suppression is discussed.
mRNA降解是基因表达调控中的一个重要控制点,并且与翻译过程相关联。这种关联的一个明显例子是非义介导的mRNA降解途径,其中基因中的无义突变可降低从该基因转录的mRNA的丰度。对于酿酒酵母而言,Upf1蛋白(Upf1p)含有富含半胱氨酸和组氨酸的区域以及核苷三磷酸水解和解旋酶基序,已被证明是该降解途径中的反式作用因子。对野生型Upf1p的生化分析表明,它具有RNA依赖性ATP酶、RNA解旋酶和RNA结合活性。UPF1基因破坏导致含无义的mRNA稳定化,从而产生足够的功能性产物以克服由无义突变引起的营养缺陷。为了理解Upf1p在无义介导的mRNA降解途径中的功能机制,对UPF1基因进行了遗传和生化研究。我们的分析表明,Upf1p是一种多功能蛋白,具有可分离的活性,可影响mRNA周转和无义抑制。已鉴定出Upf1p保守解旋酶基序中的突变,这些突变使其mRNA降解功能失活,同时不允许抑制leu2-2和tyr7-1无义等位基因。特别是,位于Upf1p的ATP结合和水解基序中的一个突变,将天冬氨酸和谷氨酸残基变为丙氨酸残基(DE572AA),缺乏ATP酶和解旋酶活性,并且该突变体在没有ATP的情况下形成Upf1p:RNA复合物;然而,令人惊讶的是,由于ATP结合,Upf1p:RNA复合物解离。该结果表明,对于该突变蛋白,ATP结合独立于其水解可调节Upf1p:RNA复合物的形成。讨论了Upf1p的RNA结合活性在调节无义抑制中的作用。