A nucleosome-free dG-dC-rich sequence element promotes constitutive transcription of the essential yeast RIO1 gene

被引:6
作者
Angermayr, M [1 ]
Schwerdtfeger, K [1 ]
Bandlow, W [1 ]
机构
[1] Univ Munich, Dept Biol 1, Bereich Genet, D-80638 Munich, Germany
关键词
chromatin analysis (in vivo footprinting); constitutive promoter; essential gene; gene shuffling; promoter analysis; protein serine kinase; Saccharomyces cerevisiae;
D O I
10.1515/BC.2003.143
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
RIO1 is an essential gene that encodes a protein serine kinase and is transcribed constitutively at a very low level. Transcriptional activation of RIO1 dispenses with a canonical TATA box as well as with classical transactivators or specific DNAbinding factors. Instead, a dGdCrich sequence element, that is located 40 to 48 bp upstream the single site of mRNA initiation, is essential and presumably constitutes the basal promoter. In addition, we demonstrate here that this promoter element comprises a nucleosomefree gap which is centered at the dGdC tract and flanked by two positioned nucleosomes. This element is both, necessary and sufficient, for basal transcription initiation at the RIO1 promoter and, thus, constitutes a novel type of core promoter element.
引用
收藏
页码:1287 / 1292
页数:6
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