Transcriptional analysis of the pst operon of Escherichia coli

被引:48
|
作者
Aguena, M
Yagil, M
Spira, B
机构
[1] Univ Sao Paulo, Inst Ciencias Biomed, Dept Microbiol, BR-05508900 Sao Paulo, Brazil
[2] Tel Aviv Univ, Dept Biochem, IL-69978 Tel Aviv, Israel
基金
巴西圣保罗研究基金会;
关键词
pst operon; PHO-regulon; Echerichia coli;
D O I
10.1007/s00438-002-0764-4
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
The pst operon of Escherichia coli, which encodes the phosphate-specific transport system, is composed of five genes, pstS, pstC, pstA, pstB and phoU, whose transcription is induced by phosphate starvation. A phosphate-regulated promoter located upstream of the most proximal gene, (pstS) controls the transcription of the entire operon. Though the full-length pst mRNA could be detected by an improved RT-PCR protocol, Northern analysis using several pst-specific probes failed to reveal this transcript. Instead, smaller but distinct pst mRNA species were evident. Primer-extension experiments localized the 5' ends of pst mRNAs within the operon. The data suggest that the full-length mRNA is rapidly processed post-transcriptionally.
引用
收藏
页码:518 / 524
页数:7
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