Zur and zinc increase expression of E. coli ribosomal protein L31 through RNA-mediated repression of the repressor L31p

Rebecca A. Rasmussen, Suning Wang, Jeannie M. Camarillo, Victoria Sosnowski, Byoung Kyu Cho, Young Ah Goo, Julius B. Lucks, Thomas V. O'Halloran

Research output: Contribution to journalArticlepeer-review

5 Scopus citations

Abstract

Bacteria can adapt in response to numerous stress conditions. One such stress condition is zinc depletion. The zinc-sensing transcription factor Zur regulates the way numerous bacterial species respond to severe changes in zinc availability. Under zinc sufficient conditions, Zn-loaded Zur (Zn2-Zur) is well-known to repress transcription of genes encoding zinc uptake transporters and paralogues of a few ribosomal proteins. Here, we report the discovery and mechanistic basis for the ability of Zur to up-regulate expression of the ribosomal protein L31 in response to zinc in E. coli. Through genetic mutations and reporter gene assays, we find that Zur achieves the up-regulation of L31 through a double repression cascade by which Zur first represses the transcription of L31p, a zinc-lacking paralogue of L31, which in turn represses the translation of L31. Mutational analyses show that translational repression by L31p requires an RNA hairpin structure within the l31 mRNA and involves the N-terminus of the L31p protein. This work uncovers a new genetic network that allows bacteria to respond to host-induced nutrient limiting conditions through a sophisticated ribosomal protein switching mechanism.

Original languageEnglish (US)
Pages (from-to)12739-12753
Number of pages15
JournalNucleic acids research
Volume50
Issue number22
DOIs
StatePublished - Dec 9 2022

Funding

FUNDING National Science Foundation Graduate Research Fellowship Program [DGE-1842165 to R.A.R.]; National Institute of General Medical Sciences of the National Institutes of Health [T32GM105538 to R.A.R., 1R01GM130901 to J.B.L., R01GM038784 to T.V.O.]. Funding for open access charge: NIH.

ASJC Scopus subject areas

  • Genetics

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