Determinants of mer Promoter Activity from Pseudomonas aeruginosa .
Qingyuan HuJue WangChunhong LiuYu FengHao ChenPublished in: Genes (2024)
Since the MerR family is known for its special regulatory mechanism, we aimed to explore which factors determine the expression activity of the mer promoter. The Tn501/Tn21 mer promoter contains an abnormally long spacer (19 bp) between the -35 and -10 elements, which is essential for the unique DNA distortion mechanism. To further understand the role of base sequences in the mer promoter spacer, this study systematically engineered a series of mutant derivatives and used luminescent and fluorescent reporter genes to investigate the expression activity of these derivatives. The results reveal that the expression activity of the mer promoter is synergistically modulated by the spacer length (17 bp is optimal) and the region upstream of -10 (especially -13G). The spacing is regulated by MerR transcription factors through symmetrical sequences, and -13G presumably functions through interaction with the RNA polymerase sigma-70 subunit.
Keyphrases
- transcription factor
- dna methylation
- poor prognosis
- gene expression
- pseudomonas aeruginosa
- genome wide
- binding protein
- cystic fibrosis
- escherichia coli
- cell free
- long non coding rna
- biofilm formation
- circulating tumor
- genome wide identification
- staphylococcus aureus
- sensitive detection
- genetic diversity
- acinetobacter baumannii
- fluorescent probe
- candida albicans
- wild type
- genome wide analysis