Olivas W, Parker R
Department of Molecular and Cellular Biology and Howard Hughes Medical Institute, University of Arizona, Tucson, AZ 85721, USA.
EMBO J. 2000 Dec 1;19(23):6602-11. doi: 10.1093/emboj/19.23.6602.
Eukaryotic post-transcriptional regulation is often specified by control elements within mRNA 3'- untranslated regions (3'-UTRs). In order to identify proteins that regulate specific mRNA decay rates in Saccharomyces cerevisae, we analyzed the role of five members of the Puf family present in the yeast genome (referred to as JSN1/PUF1, PUF2, PUF3, PUF4 and MPT5/PUF5). Yeast strains lacking all five Puf proteins showed differential expression of numerous yeast mRNAs. Examination of COX17 mRNA indicates that Puf3p specifically promotes decay of this mRNA by enhancing the rate of deadenylation and subsequent turnover. Puf3p also binds to the COX17 mRNA 3'-UTR in vitro. This indicates that the function of Puf proteins as specific regulators of mRNA deadenylation has been conserved throughout eukaryotes. In contrast to the case in Caenorhabditis elegans and Drosophila, yeast Puf3p does not affect translation of COX17 mRNA. These observations indicate that Puf proteins are likely to play a role in the control of transcript-specific rates of degradation in yeast by interacting directly with the mRNA turnover machinery.
真核生物的转录后调控通常由mRNA 3'非翻译区(3'-UTR)内的调控元件决定。为了鉴定在酿酒酵母中调节特定mRNA降解速率的蛋白质,我们分析了酵母基因组中存在的Puf家族五个成员的作用(分别称为JSN1/PUF1、PUF2、PUF3、PUF4和MPT5/PUF5)。缺乏所有五种Puf蛋白的酵母菌株显示出许多酵母mRNA的差异表达。对COX17 mRNA的检测表明,Puf3p通过提高去腺苷酸化速率和随后的周转来特异性促进该mRNA的降解。Puf3p在体外也与COX17 mRNA的3'-UTR结合。这表明Puf蛋白作为mRNA去腺苷酸化的特异性调节因子的功能在整个真核生物中保守。与秀丽隐杆线虫和果蝇的情况相反,酵母Puf3p不影响COX17 mRNA的翻译。这些观察结果表明,Puf蛋白可能通过直接与mRNA周转机制相互作用,在酵母中转录本特异性降解速率的控制中发挥作用。