Nouraini S, Hu J, McBroom L D, Friesen J D
Department of Genetics, Hospital for Sick Children, Toronto, Canada.
Yeast. 1996 Oct;12(13):1339-50. doi: 10.1002/(SICI)1097-0061(199610)12:13%3C1339::AID-YEA31%3E3.0.CO;2-C.
A binding site for the transcription factor Abf1p was identified as an important promoter element of the gene that encodes Rpo26, a subunit common to all three yeast nuclear RNA polymerases (RNAP). Mutations in the Abf1p binding site were identified among a pool of rpo26 mutant alleles that confer synthetic lethality in combination with a temperature-sensitive mutation (rpo21-4) in the gene that encodes the largest subunit of RNAPII (Rpo21p). In the presence of the wild-type allele of RPO21 these rpo26 promoter mutations confer a cold-sensitive growth defect. Electrophoretic mobility-shift assays using purified Abf1p demonstrated that Abf1p binds to the RPO26 promoter and that the promoter mutations abolish this binding in vitro. Quantitation of the amount of RPO26 mRNA showed that mutations in the Abf1p binding site reduce the expression of RPO26 by approximately 60%. Mutations that affect Abf1p binding also result in a shift of the RPO26 transcriptional start sites to positions further upstream than normal. These results suggest that binding of the Abf1p transcription factor to the RPO26 promoter is important not only in establishing the level of transcription for this gene, but also in positioning the initiation sites of transcription.
转录因子Abf1p的结合位点被确定为编码Rpo26基因的一个重要启动子元件,Rpo26是酵母三种核RNA聚合酶(RNAP)共有的一个亚基。在一组rpo26突变等位基因中发现了Abf1p结合位点的突变,这些突变与编码RNAPII最大亚基(Rpo21p)的基因中的温度敏感突变(rpo21-4)结合时会导致合成致死性。在RPO21野生型等位基因存在的情况下,这些rpo26启动子突变会导致冷敏感生长缺陷。使用纯化的Abf1p进行的电泳迁移率变动分析表明,Abf1p与RPO26启动子结合,并且启动子突变在体外消除了这种结合。对RPO26 mRNA量的定量分析表明,Abf1p结合位点的突变使RPO26的表达降低了约60%。影响Abf1p结合的突变还导致RPO26转录起始位点比正常情况向上游更远处移动。这些结果表明,Abf1p转录因子与RPO26启动子的结合不仅对于确定该基因的转录水平很重要,而且对于定位转录起始位点也很重要。