Kai Papenfort

Professor

Friedrich Schiller University Jena
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Germany

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Kai Papenfort is a Professor at Friedrich-Schiller-Universität Jena, Germany. His research primarily focuses on bacterial communication, small RNA regulation, and the role of extracellular vesicles in microbial interactions. Recent publications include studies on quorum sensing mechanisms, the influence of small RNAs on bacterial metabolism, and innovative organ-on-chip models for infectious disease research.

Articles (19)

Genome-wide profiling of Hfq-bound RNAs reveals the iron-responsive small RNA RusT in <i>Caulobacter crescentus</i>

The alphaproteobacterium Caulobacter crescentus thrives in oligotrophic environments and is able to optimally exploit minimal resources by entertaining an intricate network of gene expression control mechanisms. Numerous transcriptional activators and repressors have been reported to contribute to these processes, but only few studies have focused on regulation at the post-transcriptional level in C. crescentus . Small RNAs (sRNAs) are a prominent class of regulators of bacterial gene expression, and most sRNAs characterized today engage in direct base-pairing interactions to modulate the translation and/or stability of target mRNAs. In many cases, the ubiquitous RNA chaperone, Hfq, contributes to the establishment of RNA-RNA interactions. Although the deletion of the hfq gene is associated with a severe loss of fitness in C. crescentus , the RNA ligands of the chaperone have remained largely unexplored. Here we report on the identification of coding and non-coding transcripts associated with Hfq in C. crescentus and demonstrate Hfq-dependent post-transcriptional regulation in this organism. We show that the Hfq-bound sRNA RusT is transcriptionally controlled by the NtrYX two-component system and induced in response to iron starvation. By combining RusT pulse expression with whole-genome transcriptome analysis, we determine 16 candidate target transcripts that are deregulated, many of which encode outer membrane transporters. We hence suggest RusT to support remodeling of the C. crescentus cell surface when iron supplies are limited. IMPORTANCE The conserved RNA-binding protein Hfq contributes significantly to the adaptation of bacteria to different environmental conditions. Hfq not only stabilizes associated sRNAs but also promotes inter-molecular base-pairing interactions with target transcripts. Hfq plays a pivotal role for growth and survival, controlling central metabolism and cell wall synthesis in the oligotroph Caulobacter crescentus . However, direct evidence for Hfq-dependent post-transcriptional regulation and potential oligotrophy in C. crescentus has been lacking. Here, we identified sRNAs and mRNAs associated with Hfq in vivo , and demonstrated the requirement of Hfq for sRNA-mediated regulation, particularly of outer membrane transporters in C. crescentus .

Year:

2024

Collaborators (8)

Patrick H Viollier

-

SWITZERLAND

Ruman Gerst

Leibniz-Institut für Naturstoff-Forschung und Infektionsbiologie eV Hans-Knöll-Institut

GERMANY

Sacha Pidot

Senior lecturer/Group leader

University of Melbourne

AUSTRALIA

Praveen Kumar Singh

RWTH Aachen University

GERMANY

Kathrin S. Fröhlich

-

GERMANY

Alexander Goesmann

Full professor

Justus Liebig Universitat Giessen

GERMANY

Kai Thormann

Justus Liebig Universitat Giessen

GERMANY

Sarah Woodson

Professor

Johns Hopkins University

UNITED STATES
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