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大肠杆菌K12中ilvY和ilvC基因的核苷酸序列及体内表达。来自反向重叠启动子的转录。

Nucleotide sequence and in vivo expression of the ilvY and ilvC genes in Escherichia coli K12. Transcription from divergent overlapping promoters.

作者信息

Wek R C, Hatfield G W

出版信息

J Biol Chem. 1986 Feb 15;261(5):2441-50.

PMID:3003115
Abstract

The ilvC gene of Escherichia coli K12 encodes acetohydroxy acid isomeroreductase, the second enzyme in the parallel isoleucine-valine biosynthetic pathway. Previous data have shown that transcription of the ilvC gene is induced by the acetohydroxy acid isomeroreductase substrates, acetohydroxybutyrate or acetolactate, and that this substrate induction of ilvC expression is mediated by a positive activator encoded by the ilvY gene. We report here the isolation and complete nucleotide sequence of the ilvY and ilvC genes. The ilvY and ilvC genes encode polypeptides of Mr 33,200 and 54,000, respectively. In vitro transcription-translation of these gene templates results in the synthesis of gene products of these identical molecular weights. The ilvC gene is transcribed in the same direction as the genes of the adjacent ilvGMEDA operon. The ilvY gene is transcribed in a direction opposite to the ilvC and ilvGMEDA genes. The in vivo transcriptional initiation sites of the ilvY and ilvC genes have been determined by S1 nuclease protection experiments. These transcriptional initiation sites are 45 nucleotides apart, and transcription of the ilvY and ilvC genes is initiated via divergent overlapping promoters. The nucleotide sequence of the ilvY and ilvC promoters and 5'-coding regions of Salmonella typhimurium LT2 have been determined. A comparison of these sequences with E. coli K12 suggests regions important in the promotion, regulation, and translation of the ilvY and ilvC genes. A model is presented in which the ilvY-encoded activator binds to an operator site in the overlapping promoter region and reciprocally regulates the transcription of the ilvY and ilvC genes. The carboxyl-terminal amino acid sequence of threonine deaminase encoded by the ilvA gene of the ilv-GMEDA operon of E. coli K12 has been identified by homology with the previously deduced threonine deaminase amino acid sequence encoded by the ilv1 gene of Saccharomyces cerevisiae. Based on the deduced amino acid sequences of the ilvA and ilvY genes, the translational termination codons for both genes are shown to be separated by 52 nucleotides. The proximity of the ilvA and ilvY genes suggests that the 3'-ends of these transcripts overlap.

摘要

大肠杆菌K12的ilvC基因编码乙酰羟酸异构还原酶,这是异亮氨酸-缬氨酸平行生物合成途径中的第二种酶。先前的数据表明,ilvC基因的转录由乙酰羟酸异构还原酶的底物乙酰羟丁酸或乙酰乳酸诱导,并且ilvC表达的这种底物诱导是由ilvY基因编码的一种正激活剂介导的。我们在此报告ilvY和ilvC基因的分离及完整核苷酸序列。ilvY和ilvC基因分别编码分子量为33200和54000的多肽。这些基因模板的体外转录-翻译导致合成这些相同分子量的基因产物。ilvC基因与相邻的ilvGMEDA操纵子的基因转录方向相同。ilvY基因的转录方向与ilvC和ilvGMEDA基因相反。ilvY和ilvC基因的体内转录起始位点已通过S1核酸酶保护实验确定。这些转录起始位点相隔45个核苷酸,ilvY和ilvC基因的转录通过发散重叠启动子起始。已确定鼠伤寒沙门氏菌LT2的ilvY和ilvC启动子以及5'-编码区的核苷酸序列。将这些序列与大肠杆菌K12进行比较,提示了在ilvY和ilvC基因的启动、调控及翻译中重要的区域。提出了一个模型,其中ilvY编码的激活剂与重叠启动子区域中的一个操纵位点结合,并相互调节ilvY和ilvC基因的转录。通过与先前推导的酿酒酵母ilv1基因编码的苏氨酸脱氨酶氨基酸序列进行同源性比较,确定了大肠杆菌K1 alvGMEDA操纵子的ilvA基因编码的苏氨酸脱氨酶的羧基末端氨基酸序列。根据ilvA和ilvY基因推导的氨基酸序列,显示这两个基因的翻译终止密码子相隔52个核苷酸。ilvA和ilvY基因的接近表明这些转录本的3'-末端重叠。

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