Vivier M A, Pretorius I S
Institute for Wine Biotechnology, Department of Microbiology, University of Stellenbosch 7600, South Africa.
Curr Genet. 1998 Jan;33(1):10-5. doi: 10.1007/s002940050302.
Accurate transcription by RNA polymerase II is usually dependent on the presence of a TATA element, and/or an initiator element, in the promoters of protein-encoding genes. The STA1-3 genes, encoding three glucoamylase isozymes (Sta1p, Sta2p and Sta3p, respectively) responsible for starch hydrolysis in the yeast Saccharomyces cerevisiae, have been shown to contain long and complex promoters with several regulatory regions. These promoters are also virtually identical to the yeast MUC1 gene promoter; this gene encodes a mucin-like protein and is evolutionary linked to, and transcriptionally co-regulated with, STA1-3. The STA1-3 genes contain two putative TATA sequences; one conforming to the typical TATA box sequence, TATAAA, and another with the sequence of TATAAT. Here we present a study into the functional relevance of these putative TATA sequences and their effects on the transcription of the STA2 gene (as a representative model of the STA1-3 multigene family) and, by analogy, the MUC1 gene. We show that the TATAAA motif is the functional TATA box for STA2 and influences transcript levels, transcript initiation sites, and glucoamylase activities.
RNA聚合酶II的准确转录通常取决于蛋白质编码基因启动子中TATA元件和/或起始子元件的存在。酿酒酵母中负责淀粉水解的三种葡糖淀粉酶同工酶(分别为Sta1p、Sta2p和Sta3p)的编码基因STA1-3,已被证明含有具有多个调控区域的长而复杂的启动子。这些启动子实际上也与酵母MUC1基因启动子相同;该基因编码一种黏蛋白样蛋白,与STA1-3在进化上相关联,并在转录上共同调控。STA1-3基因包含两个假定的TATA序列;一个符合典型的TATA盒序列TATAAA,另一个序列为TATAAT。在此,我们对这些假定的TATA序列的功能相关性及其对STA2基因(作为STA1-3多基因家族的代表性模型)以及类推的MUC1基因转录的影响进行了研究。我们表明,TATAAA基序是STA2的功能性TATA盒,影响转录本水平、转录起始位点和葡糖淀粉酶活性。