Stoner Christopher S, Pearson George D, Koç Ahmet, Merwin Jason R, Lopez Nathan I, Merrill Gary F
Department of Biochemistry and Biophysics, Oregon State University, 2011 ALS Building, Corvallis, Oregon 97331-7305, USA.
Biochemistry. 2009 Sep 29;48(38):9156-69. doi: 10.1021/bi900757q.
Reporter gene transactivation by human p53 is inhibited in budding yeast lacking the TRR1 gene encoding thioredoxin reductase. To investigate the role of thioredoxin in controlling p53 activity, the level of reporter gene transactivation by p53 was determined in yeast lacking the TRX1 and TRX2 genes encoding cytosolic thioredoxin. Surprisingly, p53 activity was unimpaired in yeast lacking thioredoxin. Subsequent analyses showed that thioredoxin deletion suppressed the inhibitory effect of thioredoxin reductase deletion, suggesting that accumulation of oxidized thioredoxin in mutant yeast was necessary for p53 inhibition. Purified human thioredoxin and p53 interacted in vitro (Kd = 0.9 microM thioredoxin). To test the idea that dithio-disulfide exchange reactions between p53 and thioredoxin were responsible for p53 inhibition in mutant yeast, each p53 cysteine was changed to serine, and the effect of the substitution on p53 activity in TRR1 and Deltatrr1 yeast was determined. Substitutions at Zn-coordinating cysteines C176, C238, or C242 resulted in p53 inactivation. Unexpectedly, substitution at cysteine C275 also inactivated p53, which was the first evidence for a non-zinc-coordinating cysteine being essential for p53 function. Cysteine substitutions at six positions (C124, C135, C141, C182, C229, and C277) neither inactivated p53 nor relieved the requirement for thioredoxin reductase. Furthermore, no tested combination of these six cysteine substitutions relieved thioredoxin reductase dependence. The results suggested that p53 dependence on thioredoxin reductase either was indirect, perhaps mediated by an upstream activator of p53, or was due to oxidation of one or more of the four essential cysteines.
在缺乏编码硫氧还蛋白还原酶的TRR1基因的芽殖酵母中,人p53介导的报告基因反式激活受到抑制。为了研究硫氧还蛋白在调控p53活性中的作用,我们检测了在缺乏编码胞质硫氧还蛋白的TRX1和TRX2基因的酵母中,p53介导的报告基因反式激活水平。令人惊讶的是,在缺乏硫氧还蛋白的酵母中,p53的活性并未受损。随后的分析表明,硫氧还蛋白缺失抑制了硫氧还蛋白还原酶缺失的抑制作用,这表明突变酵母中氧化型硫氧还蛋白的积累是p53抑制所必需的。纯化的人硫氧还蛋白和p53在体外相互作用(硫氧还蛋白的解离常数Kd = 0.9 microM)。为了验证p53与硫氧还蛋白之间的二硫键-二硫键交换反应是突变酵母中p53抑制的原因这一想法,我们将每个p53半胱氨酸都替换为丝氨酸,并检测了该替换对TRR1和Deltatrr1酵母中p53活性的影响。锌配位半胱氨酸C176、C238或C242的替换导致p53失活。出乎意料的是,半胱氨酸C275的替换也使p53失活,这是首个证明非锌配位半胱氨酸对p53功能至关重要的证据。六个位置(C124、C135、C141、C182、C229和C277)的半胱氨酸替换既未使p53失活,也未消除对硫氧还蛋白还原酶的需求。此外,这六个半胱氨酸替换的任何测试组合都未消除对硫氧还蛋白还原酶的依赖性。结果表明,p53对硫氧还蛋白还原酶的依赖性要么是间接的,可能由p53的上游激活剂介导,要么是由于四个必需半胱氨酸中的一个或多个被氧化所致。