Ono Bun-Ichiro, Yoshida Ryohma, Kamiya Koh, Sugimoto Tatsuzo
Department of Biotechnology, Faculty of Science and Engineering, Ritsumeikan University, Kusatsu, Shiga, Japan.
Genes Genet Syst. 2005 Oct;80(5):311-6. doi: 10.1266/ggs.80.311.
Among a large collection of nonsense (termination) suppressors of Saccharomyces cerevisiae, a few remained obscure for their molecular nature. Of those, a group of weak and recessive suppressors, sup111, sup112 and sup113, is of particular interest because of their dependency on [PSI+], a yeast prion. From the facts that these suppressors map at positions quite similar to the UPF2, UPF3 and UPF1 genes, respectively, and that some mutations in the UPF genes confer termination suppressor activity, we suspected that sup111, sup112 and sup113 would very well be mutant alleles of the UPF genes. We tested our speculation and found that sup113, sup111 and sup112 were in fact complemented with the wild-type alleles of UPF1, UPF2 and UPF3, respectively. We further obtained evidence that the UPF1, UPF2 and UPF3 loci of the strains carrying sup113, sup111 and sup112, respectively, had point mutations. From these results, we conclude that sup111, sup112 and sup113 are mutant alleles of UPF2, UPF3 and UPF1, respectively, and thus attribute suppressor activity of these mutations to defects in the NMD (nonsense-mediated mRNA decay) machinery.
在酿酒酵母的大量无义(终止)抑制子中,有一些的分子本质仍不清楚。其中,一组弱的隐性抑制子sup111、sup112和sup113特别令人感兴趣,因为它们依赖于酵母朊病毒[PSI+]。鉴于这些抑制子分别定位于与UPF2、UPF3和UPF1基因非常相似的位置,且UPF基因中的一些突变赋予终止抑制子活性,我们推测sup111、sup112和sup113很可能是UPF基因的突变等位基因。我们对这一推测进行了验证,发现sup113、sup111和sup112实际上分别被UPF1、UPF2和UPF3的野生型等位基因互补。我们进一步获得证据表明,分别携带sup113、sup111和sup112的菌株的UPF1、UPF2和UPF3位点存在点突变。从这些结果中,我们得出结论,sup111、sup112和sup113分别是UPF2、UPF3和UPF1的突变等位基因,因此将这些突变的抑制子活性归因于无义介导的mRNA降解(NMD)机制的缺陷。