Promoters and transcripts associated with the aroP gene of Escherichia coli.

AUTOR(ES)

Wang, P

RESUMO

Analysis of in vitro transcriptional events initiating within the region immediately upstream of the aroP coding region has revealed the presence of three promoters, P1, P2, and P3. Both P1 and P2 give rise to mRNA encoding the AroP protein, whereas P3 initiates transcription in the opposite direction. Both P1 and P3 contain UP elements which contribute to promoter strength. Regulation of expression from these three promoters has been examined in vitro by using supercoiled DNA templates and in vivo by using lacZ transcriptional fusions and specific promoter mutants. Expression from P2 is partially repressed by TyrR alone both in vitro and in vivo. Addition of the aromatic amino acid tyrosine, phenylalanine, or tryptophan further increases this repression. P1 is not repressed by TyrR alone but is repressed in vivo in the presence of phenylalanine, tyrosine, or tryptophan. This also occurs in vitro but requires Ca2+ ions in the reaction mixture for its demonstration. Under these conditions, transcription from P3 is enhanced by TyrR protein with phenylalanine, tyrosine, or tryptophan. However, we were unable to demonstrate P3 expression in vivo. Under repressing conditions, there is no production of truncated RNA molecules (from P1), which would be expected if repression involved a roadblock mechanism.

Documentos Relacionados

• Cloning of the aroP gene and identification of its product in Escherichia coli K-12.
• Repression of the aroP gene of Escherichia coli involves activation of a divergent promoter.
• Transcription control of the aroP gene in Escherichia coli K-12: analysis of operator mutants.
• A topological model for the general aromatic amino acid permease, AroP, of Escherichia coli.
• Mechanism of Repression of the aroP P2 Promoter by the TyrR Protein of Escherichia coli