Tijerina P, Sayre M H
Department of Biochemistry, Johns Hopkins University School of Hygiene and Public Health, Baltimore, Maryland 21205, USA.
J Biol Chem. 1998 Jan 9;273(2):1107-13. doi: 10.1074/jbc.273.2.1107.
The influence of transcription factor (TF) IIE on mRNA synthesis in vivo was examined in a temperature-sensitive yeast mutant. A missense mutation in the conserved zinc finger domain severely weakened TFIIE's transcription activity without appreciably affecting its quaternary structure, chromatographic properties, or cellular abundance. The mutation conferred recessive slow-growth and heat-sensitive phenotypes in yeast, but quantitative effects on promoter utilization by RNA polymerase II ranged from strongly negative to somewhat positive. Heat-induced activation of the HSP26, HSP104, and SSA4 genes was attenuated in the mutant, indicating dependence on TFIIE for maximal rates of de novo synthesis. Constitutive HSP expression in mutant cells was elevated, exposing a negative (likely indirect) influence by TFIIE in the absence of heat stress. Our results corroborate and extend recent findings of differential dependence on TFIIE activity for yeast promoters, but reveal an important counterpoint to the notion that dependence is tied to TATA element structure (Sakurai, H., Ohishi, T., and Fukasawa, T. (1997) J. Biol. Chem. 272, 15936-15942). We also provide empirical evidence for conservation of structure-activity relationships in TFIIE's zinc finger domain, and establish a direct link between TFIIE's biochemical activity in reconstituted transcription and its function in cellular mRNA synthesis.
在一个温度敏感型酵母突变体中研究了转录因子(TF)IIE对体内mRNA合成的影响。保守锌指结构域中的一个错义突变严重削弱了TFIIE的转录活性,而对其四级结构、色谱性质或细胞丰度没有明显影响。该突变在酵母中赋予隐性的生长缓慢和热敏感表型,但对RNA聚合酶II对启动子的利用的定量影响范围从强烈负向到有些正向。突变体中热诱导的HSP26、HSP104和SSA4基因的激活减弱,表明从头合成的最大速率依赖于TFIIE。突变体细胞中组成型HSP表达升高,揭示了在无热应激时TFIIE的负向(可能是间接的)影响。我们的结果证实并扩展了最近关于酵母启动子对TFIIE活性差异依赖性的发现,但揭示了一个与依赖性与TATA元件结构相关这一观点重要的对立观点(樱井,H.,大石,T.,和深泽,T.(1997)《生物化学杂志》272,15936 - 15942)。我们还为TFIIE锌指结构域中结构 - 活性关系的保守性提供了经验证据,并在重组转录中TFIIE的生化活性与其在细胞mRNA合成中的功能之间建立了直接联系。