Madden S L, Johnson D L, Bergman L W
Department of Chemistry, Clippinger Laboratories, Ohio University, Athens 45701-2979.
Mol Cell Biol. 1990 Nov;10(11):5950-7. doi: 10.1128/mcb.10.11.5950-5957.1990.
The PHO80 and PHO85 gene products encode proteins necessary for the repression of transcription from the major acid phosphatase gene (PHO5) of Saccharomyces cerevisiae. The deduced amino acid sequences of these genes have revealed that PHO85 is likely to encode a protein kinase, whereas no potential function has been revealed for PHO80. We undertook several approaches to aid in the elucidation of the PHO80 function, including deletion analysis, chemical mutagenesis, and expression analysis. DNA deletion analysis revealed that residues from both the carboxy- and amino-terminal regions of the protein, amounting to a total of 21% of the PHO80 protein, were not required for function with respect to repressor activity. Also, 10 independent single-amino-acid changes within PHO80 which resulted in the failure to repress PHO5 transcription were isolated. Nine of the 10 missense mutations resided in two subregions of the PHO80 molecule. In addition, expression analysis of the PHO80 and PHO85 genes suggested that the PHO85 gene product was not necessary for PHO80 expression and that the PHO85 gene was expressed at much higher levels in the cell than was the PHO80 gene. Furthermore, high levels of PHO80 were shown to suppress the effect of a PHO85 deletion at a level close to full repression. Implications for the function of the negative regulators in this system are discussed.
PHO80和PHO85基因产物编码了酿酒酵母主要酸性磷酸酶基因(PHO5)转录抑制所必需的蛋白质。这些基因推导的氨基酸序列显示,PHO85可能编码一种蛋白激酶,而PHO80尚未揭示潜在功能。我们采取了几种方法来帮助阐明PHO80的功能,包括缺失分析、化学诱变和表达分析。DNA缺失分析表明,该蛋白质羧基端和氨基端区域的残基,总计占PHO80蛋白的21%,对于阻遏物活性的功能并非必需。此外,分离出了PHO80内10个导致无法抑制PHO5转录的独立单氨基酸变化。10个错义突变中的9个位于PHO80分子的两个亚区域。另外,PHO80和PHO85基因的表达分析表明,PHO85基因产物对于PHO80的表达并非必需,并且PHO85基因在细胞中的表达水平远高于PHO80基因。此外,高水平的PHO80被证明能在接近完全抑制的水平上抑制PHO85缺失的影响。本文讨论了该系统中负调控因子功能的意义。