Séron K, Blondel M O, Haguenauer-Tsapis R, Volland C
Institut Jacques Monod, CNRS/Université Paris 7-Denis Diderot 2, 75251 Paris Cedex 05, France.
J Bacteriol. 1999 Mar;181(6):1793-800. doi: 10.1128/JB.181.6.1793-1800.1999.
In Saccharomyces cerevisiae the FUR4-encoded uracil permease catalyzes the first step of the pyrimidine salvage pathway. The availability of uracil has a negative regulatory effect upon its own transport. Uracil causes a decrease in the level of uracil permease, partly by decreasing the FUR4 mRNA level in a promoter-independent fashion, probably by increasing its instability. Uracil entry also triggers more rapid degradation of the existing permease by promoting high efficiency of ubiquitination of the permease that signals its internalization. A direct binding of intracellular uracil to the permease is possibly involved in this feedback regulation, as the behavior of the permease is similar in mutant cells unable to convert intracellular uracil into UMP. We used cells impaired in the ubiquitination step to show that the addition of uracil produces rapid inhibition of uracil transport. This may be the first response prior to the removal of the permease from the plasma membrane. Similar down-regulation of uracil uptake, involving several processes, was observed under adverse conditions mainly corresponding to a decrease in the cellular content of ribosomes. These results suggest that uracil of exogenous or catabolic origin down-regulates the cognate permease to prevent buildup of excess intracellular uracil-derived nucleotides.
在酿酒酵母中,由FUR4编码的尿嘧啶通透酶催化嘧啶补救途径的第一步。尿嘧啶的可用性对其自身的转运具有负调控作用。尿嘧啶会导致尿嘧啶通透酶水平降低,部分原因是通过不依赖启动子的方式降低FUR4 mRNA水平,可能是通过增加其不稳定性。尿嘧啶的进入还通过促进对通透酶进行高效泛素化(这标志着通透酶的内化)来触发现有通透酶更快地降解。细胞内尿嘧啶与通透酶的直接结合可能参与了这种反馈调节,因为在无法将细胞内尿嘧啶转化为UMP的突变细胞中,通透酶的行为是相似的。我们使用在泛素化步骤中受损的细胞来表明添加尿嘧啶会迅速抑制尿嘧啶转运。这可能是在通透酶从质膜上移除之前的第一个反应。在主要对应于核糖体细胞含量降低的不利条件下,观察到了涉及多个过程的类似尿嘧啶摄取下调。这些结果表明,外源性或分解代谢来源的尿嘧啶会下调同源通透酶,以防止细胞内过量尿嘧啶衍生核苷酸的积累。