Nat Commun. 2020 Dec 22;11(1):6430. doi: 10.1038/s41467-020-20181-5. | PubMed

Nick D Pokorzynski^1,2, Nathan D Hatch², Scot P Ouellette², Rey A Carabeo³

1. School of Molecular Biosciences, College of Veterinary Medicine, Washington State University, Pullman, WA, USA.
2. Department of Pathology and Microbiology, University of Nebraska Medical Center, Omaha, NE, USA.
3. Department of Pathology and Microbiology, University of Nebraska Medical Center, Omaha, NE, USA. rey.carabeo@unmc.edu.

Abstract

The trp operon of Chlamydia trachomatis is organized differently from other model bacteria. It contains trpR, an intergenic region (IGR), and the biosynthetic trpB and trpA open-reading frames. TrpR is a tryptophan-dependent repressor that regulates the major promoter (PtrpR), while the IGR harbors an alternative promoter (PtrpBA) and an operator sequence for the iron-dependent repressor YtgR to regulate trpBA expression. Here, we report that YtgR repression at PtrpBA is also dependent on tryptophan by regulating YtgR levels through a rare triple-tryptophan motif (WWW) in the YtgCR precursor. Inhibiting translation during tryptophan limitation at the WWW motif subsequently promotes Rho-independent transcription termination of ytgR, thereby de-repressing PtrpBA. Thus, YtgR represents an alternative strategy to attenuate trpBA expression, expanding the repertoire for trp operon attenuation beyond TrpL- and TRAP-mediated mechanisms described in other bacteria. Furthermore, repurposing the iron-dependent repressor YtgR underscores the fundamental importance of maintaining tryptophan-dependent attenuation of the trpRBA operon.

Presented By Nick D Pokorzynski | ORCID iD