Ben-Yehuda S, Dix I, Russell C S, McGarvey M, Beggs J D, Kupiec M
Department of Molecular Microbiology and Biotechnology, Tel Aviv University, Ramat Aviv 69978, Israel.
Genetics. 2000 Dec;156(4):1503-17. doi: 10.1093/genetics/156.4.1503.
The PRP17/CDC40 gene of Saccharomyces cerevisiae functions in two different cellular processes: pre-mRNA splicing and cell cycle progression. The Prp17/Cdc40 protein participates in the second step of the splicing reaction and, in addition, prp17/cdc40 mutant cells held at the restrictive temperature arrest in the G2 phase of the cell cycle. Here we describe the identification of nine genes that, when mutated, show synthetic lethality with the prp17/cdc40Delta allele. Six of these encode known splicing factors: Prp8p, Slu7p, Prp16p, Prp22p, Slt11p, and U2 snRNA. The other three, SYF1, SYF2, and SYF3, represent genes also involved in cell cycle progression and in pre-mRNA splicing. Syf1p and Syf3p are highly conserved proteins containing several copies of a repeated motif, which we term RTPR. This newly defined motif is shared by proteins involved in RNA processing and represents a subfamily of the known TPR (tetratricopeptide repeat) motif. Using two-hybrid interaction screens and biochemical analysis, we show that the SYF gene products interact with each other and with four other proteins: Isy1p, Cef1p, Prp22p, and Ntc20p. We discuss the role played by these proteins in splicing and cell cycle progression.
酿酒酵母的PRP17/CDC40基因在两个不同的细胞过程中发挥作用:前体mRNA剪接和细胞周期进程。Prp17/Cdc40蛋白参与剪接反应的第二步,此外,在限制温度下培养的prp17/cdc40突变细胞在细胞周期的G2期停滞。在此,我们描述了九个基因的鉴定,这些基因在发生突变时,与prp17/cdc40Δ等位基因表现出合成致死性。其中六个基因编码已知的剪接因子:Prp8p、Slu7p、Prp16p、Prp22p、Slt11p和U2 snRNA。另外三个基因,SYF1、SYF2和SYF3,代表也参与细胞周期进程和前体mRNA剪接的基因。Syf1p和Syf3p是高度保守的蛋白质,含有几个重复基序的拷贝,我们将其称为RTPR。这个新定义的基序由参与RNA加工的蛋白质共享,代表已知TPR(四肽重复)基序的一个亚家族。通过双杂交相互作用筛选和生化分析,我们表明SYF基因产物彼此之间以及与其他四种蛋白质相互作用:Isy1p、Cef1p、Prp22p和Ntc20p。我们讨论了这些蛋白质在剪接和细胞周期进程中所起的作用。