Jarvis E E, Hagen D C, Sprague G F
Department of Biology, University of Oregon, Eugene 97403.
Mol Cell Biol. 1988 Jan;8(1):309-20. doi: 10.1128/mcb.8.1.309-320.1988.
STE3 mRNA is present only in Saccharomyces cerevisiae alpha cells, not in a or a/alpha cells, and the transcript level increases about fivefold when cells are treated with a-factor mating pheromone. Deletions in the 5' noncoding region of STE3 defined a 43-base-pair (bp) upstream activation sequence (UAS) that can impart both modes of regulation to a CYC1-lacZ fusion when substituted for the native CYC1 UAS. UAS activity required the alpha 1 product of MAT alpha, which is known to be required for transcription of alpha-specific genes. A chromosomal deletion that removed only 14 bp of the STE3 UAS reduced STE3 transcript levels 50- to 100-fold, indicating that the UAS is essential for expression. The STE3 UAS shares a 26-bp homology with the 5' noncoding sequences of the only other known alpha-specific genes, MF alpha 1 and MF alpha 2. We view the homology as having two components--a nearly palindromic 16-bp "P box" and an adjacent 10-bp "Q box." A synthetic STE3 P box was inactive as a UAS; a perfect palindrome P box was active in all three cell types. We propose that the P box is the binding site for a transcription activator, but that alpha 1 acting via the Q box is required for this activator to bind to the imperfect P boxes of alpha-specific genes. Versions of the P box are also found upstream of a-specific genes, within the binding sites of the repressor alpha 2 encoded by MAT alpha. Thus, the products of MAT alpha may render gene expression alpha or a-specific by controlling access of the same transcription activator to its binding site, the P box.
STE3信使核糖核酸仅存在于酿酒酵母α细胞中,而不存在于a细胞或a/α细胞中,当细胞用a因子交配信息素处理时,转录水平增加约五倍。STE3 5'非编码区的缺失定义了一个43个碱基对(bp)的上游激活序列(UAS),当它替代天然CYC1 UAS时,可赋予CYC1-乳糖酶Z融合蛋白两种调控模式。UAS活性需要MATα的α1产物,已知该产物是α特异性基因转录所必需的。一个仅去除STE3 UAS 14 bp的染色体缺失使STE3转录水平降低了50至100倍,表明UAS对表达至关重要。STE3 UAS与仅有的其他已知α特异性基因MFα1和MFα2的5'非编码序列有26 bp的同源性。我们认为这种同源性有两个组成部分——一个近乎回文的16 bp“P盒”和一个相邻的10 bp“Q盒”。一个合成的STE3 P盒作为UAS无活性;一个完美的回文P盒在所有三种细胞类型中都有活性。我们提出P盒是转录激活因子的结合位点,但通过Q盒起作用的α1是该激活因子与α特异性基因的不完美P盒结合所必需的。在a特异性基因的上游、MATα编码的阻遏物α2的结合位点内也发现了P盒的变体。因此,MATα的产物可能通过控制同一转录激活因子对其结合位点P盒的访问来使基因表达具有α或a特异性。