scholarly journals Control of Gene Expression from the SUC2 Promoter of Saccharomyces cerevisiae using Two Carbon Sources.

1992 ◽  
Vol 18 (5) ◽  
pp. 693-700 ◽  
Author(s):  
Takayuki Ohshima ◽  
Xiao-Li Zhang ◽  
Shinji Iijima ◽  
Takeshi Kobayashi ◽  
Fumio Hishinuma
1989 ◽  
Vol 32 (3) ◽  
Author(s):  
Kong Hua Lin ◽  
Shinji Iijima ◽  
Kazuyuki Shimizu ◽  
Fumio Hishinuma ◽  
Takeshi Kobayashi

PLoS ONE ◽  
2016 ◽  
Vol 11 (2) ◽  
pp. e0148320 ◽  
Author(s):  
Anssi Rantasalo ◽  
Elena Czeizler ◽  
Riitta Virtanen ◽  
Juho Rousu ◽  
Harri Lähdesmäki ◽  
...  

2012 ◽  
Vol 14 (2) ◽  
pp. 91-103 ◽  
Author(s):  
Gionata Scalcinati ◽  
Christoph Knuf ◽  
Siavash Partow ◽  
Yun Chen ◽  
Jérôme Maury ◽  
...  

2008 ◽  
Vol 190 (11) ◽  
pp. 3930-3939 ◽  
Author(s):  
S. James L. Cariss ◽  
Amy E. Tayler ◽  
Matthew B. Avison

ABSTRACT CreBC is a two-component system that controls the expression of a number of genes in Escherichia coli (called the cre regulon) that encode diverse functions, including intermediary metabolic enzymes. Using a reporter construct, we have shown that cre regulon gene expression is activated during growth in minimal media when glycolytic carbon sources are being fermented. It also is activated during aerobic growth when fermentation products are being used as carbon sources. CreB and CreC are essential for the activation of cre regulon gene expression, but CreA and CreD, encoded as part of the creABCD gene cluster, are not. CreB binds to a TTCACnnnnnnTTCAC direct repeat (the cre tag) in vitro, and this sequence, which is associated with cre regulon gene promoters, is required for the control of gene expression in vivo. These observations support the hypothesis that CreBC is a functional two-component system involved in the metabolic control of transcription in E. coli and confirm that CreB is a DNA binding transcriptional regulator.


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