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Negative autoregulation of cysB in Salmonella typhimurium: in vitro interactions of CysB protein with the cysB promoter.

机译:鼠伤寒沙门氏菌中cysB的负自动调节:CysB蛋白与cysB启动子的体外相互作用。

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摘要

CysB protein positively regulates genes of the Salmonella typhimurium cysteine regulon and negatively autoregulates cysB. The cysB promoter was characterized by primer extension of cellular RNA, which gave products identifying a major in vivo transcription start site located 95 bp upstream of the cysB start codon and two minor sites located 9 and 10 bp downstream of the major site. Gel shift binding studies and DNase I footprinting experiments showed that CysB protein binds to the cysB promoter from position -10 to +36 relative to the major transcription start site. We have designated this binding site CBS-B. CysB protein inhibited transcription initiation at the cysB promoter in an in vitro runoff assay, indicating that cysB is negatively autoregulated by the binding of CysB protein to the cysB promoter, where it acts as a repressor. N-Acetyl-L-serine, an inducer of the cysteine regulon, inhibited the binding of CysB protein to the cysB promoter and partially reversed the ability of CysB protein to inhibit transcription initiation. These effects are in contrast to those observed in studies of positively regulated cys promoters, in which N-acetyl-L-serine stimulates binding and causes CysB protein to activate transcription initiation.
机译:CysB蛋白可正向调节鼠伤寒沙门氏菌半胱氨酸调节子的基因,而负向自动调节cysB。 cysB启动子的特征在于细胞RNA的引物延伸,从而提供了可识别位于cysB起始密码子上游95 bp的主要体内转录起始位点和位于主要位点下游9和10 bp的两个次要位点的产物。凝胶移位结合研究和DNase I足迹实验表明,CysB蛋白相对于主要转录起始位点从-10到+36位置与cysB启动子结合。我们已将该结合位点指定为CBS-B。在体外径流测定中,CysB蛋白抑制了cysB启动子的转录起始,这表明cysB通过CysB蛋白与cysB启动子的结合而负向自动调节,在该处它充当阻遏物。 N-乙酰基-L-丝氨酸,半胱氨酸调节子的诱导剂,抑制CysB蛋白与cysB启动子的结合,并部分逆转CysB蛋白抑制转录起始的能力。这些作用与在正调节的cys启动子研究中观察到的相反,在该研究中,N-乙酰基-L-丝氨酸刺激结合并导致CysB蛋白激活转录起始。

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  • 作者

    Ostrowski, J; Kredich, N M;

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  • 年度 1991
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