Gygi S P, Rochon Y, Franza B R, Aebersold R
Department of Molecular Biotechnology, University of Washington, Seattle, Washington 98195-7730, USA.
Mol Cell Biol. 1999 Mar;19(3):1720-30. doi: 10.1128/MCB.19.3.1720.
We have determined the relationship between mRNA and protein expression levels for selected genes expressed in the yeast Saccharomyces cerevisiae growing at mid-log phase. The proteins contained in total yeast cell lysate were separated by high-resolution two-dimensional (2D) gel electrophoresis. Over 150 protein spots were excised and identified by capillary liquid chromatography-tandem mass spectrometry (LC-MS/MS). Protein spots were quantified by metabolic labeling and scintillation counting. Corresponding mRNA levels were calculated from serial analysis of gene expression (SAGE) frequency tables (V. E. Velculescu, L. Zhang, W. Zhou, J. Vogelstein, M. A. Basrai, D. E. Bassett, Jr., P. Hieter, B. Vogelstein, and K. W. Kinzler, Cell 88:243-251, 1997). We found that the correlation between mRNA and protein levels was insufficient to predict protein expression levels from quantitative mRNA data. Indeed, for some genes, while the mRNA levels were of the same value the protein levels varied by more than 20-fold. Conversely, invariant steady-state levels of certain proteins were observed with respective mRNA transcript levels that varied by as much as 30-fold. Another interesting observation is that codon bias is not a predictor of either protein or mRNA levels. Our results clearly delineate the technical boundaries of current approaches for quantitative analysis of protein expression and reveal that simple deduction from mRNA transcript analysis is insufficient.
我们已经确定了在对数中期生长的酿酒酵母中表达的选定基因的mRNA与蛋白质表达水平之间的关系。通过高分辨率二维(2D)凝胶电泳分离总酵母细胞裂解物中所含的蛋白质。切除了150多个蛋白质斑点,并通过毛细管液相色谱-串联质谱(LC-MS/MS)进行鉴定。通过代谢标记和闪烁计数对蛋白质斑点进行定量。根据基因表达序列分析(SAGE)频率表计算相应的mRNA水平(V. E. 韦尔库列斯库、L. 张、W. 周、J. 沃格尔斯坦、M. A. 巴斯莱、D. E. 巴塞特、小P. 希特、B. 沃格尔斯坦和K. W. 金兹勒,《细胞》88:243 - 251,1997)。我们发现mRNA与蛋白质水平之间的相关性不足以从定量mRNA数据预测蛋白质表达水平。实际上,对于某些基因,虽然mRNA水平相同,但蛋白质水平变化超过20倍。相反,观察到某些蛋白质的稳态水平不变,而各自的mRNA转录水平变化高达30倍。另一个有趣的观察结果是密码子偏好性既不是蛋白质水平的预测指标,也不是mRNA水平的预测指标。我们的结果清楚地划定了当前蛋白质表达定量分析方法的技术界限,并表明仅从mRNA转录本分析进行简单推断是不够的。