Transcriptional autoregulation by Mycobacterium tuberculosis PhoP involves recognition of novel direct repeat sequences in the regulatory region of the promoter

• Published in: FEBS letters 2006-10, Vol.580 (22), p.5328-5338
• Main Authors: Gupta, Sankalp, Sinha, Akesh, Sarkar, Dibyendu
• Format: Article
• Language: English
• Subjects: [N-(2 hydroxyethyl)] piperazine-N′-[2-ethanesulphonic acid]; Animals; Autoregulation; Bacterial Proteins - genetics; Bacterial Proteins - metabolism; Direct repeat units; DNA–protein interactions; EDTA; ethylene diamine tetra-acetic acid; Gene Expression Regulation, Bacterial - genetics; HEPES; Homeostasis - genetics; Humans; IPTG; isopropyl β-d-thiogalactopyranoside; Macrophages - microbiology; Mice; Mycobacterium tuberculosis; Mycobacterium tuberculosis - genetics; Mycobacterium tuberculosis - metabolism; Mycobacterium tuberculosis - pathogenicity; nitrilotriacetic acid; NTA; open reading frame; ORF; PAGE; phenylmethylsulfonyl-fluoride; PhoP-binding site; Phosphorylation; PMSF; polyacrylamide gel electrophoresis; Protein Processing, Post-Translational - genetics; Repetitive Sequences, Nucleic Acid - genetics; Response Elements - genetics; SDS; Signal Transduction - genetics; sodium dodecyl sulfate; Transcription, Genetic
• ISSN: 0014-5793; 1873-3468
• DOI: 10.1016/j.febslet.2006.09.004

The PhoP–PhoR two-component system is essential for virulence and intracellular growth of Mycobacterium tuberculosis (MTB) in human and mouse macrophages or in mice. Here, PhoP and truncated PhoR sensor proteins were shown to participate in phosphotransfer reactions using conserved residues characteristic of two-component signaling systems. β-Galactosidase activity originating from phoP promoter- lacZ construct was inhibited in presence of PhoP, suggesting transcriptional auto-inhibition by the response regulator. In vitro binding of PhoP is consistent with the in vivo transcriptional repression, indicating phosphorylation-independent assembly of the transcription initiation complex at elevated concentrations of PhoP. DNaseI protection studies reveal a consensus recognition sequence within the phoP promoter that includes three 9-bp direct repeat units. Each repeat unit adjusts to the consensus 1 AC T / G T / G T / G P y AP u C 9 . Alteration in the sequence of the newly-identified direct repeat units relieved phoP transcriptional repression in presence of PhoP, suggesting that PhoP represses its own expression by sequence-specific interaction(s) with the repeat units. Together, these results identify so far unknown PhoP-regulated genetic determinants in the regulatory region of the phoP promoter that are central to understanding of how PhoP may possibly function as a global regulator in MTB.