TRANSCRIPTIONAL REGULATION BY AN UPSTREAM REPRESSION SEQUENCE FROM THE YEAST ENOLASE GENE ENO1

被引:7
作者
CARMEN, AA [1 ]
BRINDLE, PK [1 ]
PARK, CS [1 ]
HOLLAND, MJ [1 ]
机构
[1] UNIV CALIF DAVIS,SCH MED,DEPT BIOL CHEM,DAVIS,CA 95616
关键词
ENO1; REPRESSION;
D O I
10.1002/yea.320111105
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 [生物化学与分子生物学]; 081704 [应用化学];
摘要
The activity of an upstream repression sequence (URS element) that mediates a 20-fold repression of ENO1 expression in cells grown in a medium containing glucose was characterized. Sequences that are sufficient for orientation-dependent ENO1 URS element activity were mapped between positions -241 and -126 relative to the ENO1 transcriptional initiation site. The ENO1 URS element repressed transcription of the yeast CYC1 gene when positioned between the CYC1 upstream activation sequences (UAS elements) and TATAAA boxes. The ENO1 URS element failed to repress transcription of the wild-type yeast enolase gene ENO2; however, expression of an ENO2 gene lacking one of the ENO2 UAS elements was efficiently repressed by the ENO1 URS element, suggesting that the URS element interferes with the transcriptional activation by some, but not all, UAS elements. In contrast to the ENO1 gene, the ENO1 URS element repressed CYC1 and ENO2 expression in cells grown on glucose or glycerol plus lactate. Evidence is presented that the ENO1 URS element also functions during stationary growth phase.
引用
收藏
页码:1031 / 1043
页数:13
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