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Divergent Evolution of Legionella RCC1 Repeat Effectors Defines the Range of Ran GTPase Cycle Targets

Authors :
Swart, A Leoni
Steiner, Bernhard
Gomez-Valero, Laura
Schütz, Sabina
Hannemann, Mandy
Janning, Petra
Irminger, Michael
Rothmeier, Eva
Buchrieser, Carmen
Itzen, Aymelt
Panse, Vikram Govind
Hilbi, Hubert
Institute of Medical Microbiology [Zurich]
Universität Zürich [Zürich] = University of Zurich (UZH)
Biologie des Bactéries intracellulaires - Biology of Intracellular Bacteria
Institut Pasteur [Paris]-Centre National de la Recherche Scientifique (CNRS)
Center for Integrated Protein Science (CIPSM)
Technische Universität Munchen - Université Technique de Munich [Munich, Allemagne] (TUM)-Helmholtz-Zentrum München (HZM)-Ludwig Maximilian University of Munich [Germany] (LMU München)
Max-Planck-Institut für Molekulare Physiologie
Max-Planck-Gesellschaft
Max Von Pettenkofer Institute (MVP)
Ludwig-Maximilians-Universität München (LMU)
Institute of Biochemistry and Signal Transduction [Hamburg, Germany]
Universitaetsklinikum Hamburg-Eppendorf = University Medical Center Hamburg-Eppendorf [Hamburg] (UKE)
Research in the laboratory of H.H. was supported by the Swiss National Science Foundation (SNF
31003A_153200 and 31003A_175557), the OPO Foundation, and the Novartis Foundation for Medical-Biological Research. A. Welin was supported by a grant from the Swedish Research Council (2014-396). V.G.P. was supported by grants from the Swiss National Science Foundation, NCCR RNA & Disease, Novartis Foundation for Medical-Biological Research and the Olga Mayenfisch Foundation.
Work in the laboratory of C.B. was financed by the Institut Pasteur and by grant ANR-10-LABX-62-IBEID.
We thank Amanda Welin for performing imaging flow cytometry experiments and Nadia Keller for flow cytometry analysis.
Confocal laser scanning microscopy and imaging flow cytometry were performed using equipment of the Center of Microscopy and Image Analysis, University of Zurich. Proteomics analysis was performed at the Functional Genomics Center Zürich.
ANR-10-LABX-0062,IBEID,Integrative Biology of Emerging Infectious Diseases(2010)
University of Zurich
Hilbi, Hubert
Institut Pasteur [Paris] (IP)-Centre National de la Recherche Scientifique (CNRS)
Technische Universität Munchen - Université Technique de Munich [Munich, Allemagne] (TUM)-Ludwig-Maximilians-Universität München (LMU)-Helmholtz Zentrum München = German Research Center for Environmental Health
Source :
mBio, mBio, American Society for Microbiology, 2020, 11 (2), pp.e00405-20. ⟨10.1128/mBio.00405-20⟩, mBio, Vol 11, Iss 2, p e00405-20 (2020), mBio, 2020, 11 (2), pp.e00405-20. ⟨10.1128/mBio.00405-20⟩, mBio, Vol 11, Iss 2 (2020)
Publication Year :
2020
Publisher :
HAL CCSD, 2020.

Abstract

International audience; Legionella pneumophila governs its interactions with host cells by secreting >300 different "effector" proteins. Some of these effectors contain eukaryotic domains such as the RCC1 (regulator of chromosome condensation 1) repeats promoting the activation of the small GTPase Ran. In this report, we reveal a conserved pattern of L. pneumophila RCC1 repeat genes, which are distributed in two main clusters of strains. Accordingly, strain Philadelphia-1 contains two RCC1 genes implicated in bacterial virulence, legG1 (Legionella eukaryotic gene 1), and ppgA, while strain Paris contains only one, pieG. The RCC1 repeat effectors localize to different cellular compartments and bind distinct components of the Ran GTPase cycle, including Ran modulators and the small GTPase itself, and yet they all promote the activation of Ran. The pieG gene spans the corresponding open reading frames of legG1 and a separate adjacent upstream gene, lpg1975. legG1 and lpg1975 are fused upon addition of a single nucleotide to encode a protein that adopts the binding specificity of PieG. Thus, a point mutation in pieG splits the gene, altering the effec-tor target. These results indicate that divergent evolution of RCC1 repeat effectors defines the Ran GTPase cycle targets and that modulation of different components of the cycle might fine-tune Ran activation during Legionella infection.IMPORTANCE Legionella pneumophila is a ubiquitous environmental bacterium which, upon inhalation, causes a life-threatening pneumonia termed Legionnaires' disease. The opportunistic pathogen grows in amoebae and macrophages by employing a "type IV" secretion system, which secretes more than 300 different "effec-tor" proteins into the host cell, where they subvert pivotal processes. The function of many of these effector proteins is unknown, and their evolution has not been studied. L. pneumophila RCC1 repeat effectors target the small GTPase Ran, a molecular switch implicated in different cellular processes such as nucleocytoplasmic transport and microtubule cytoskeleton dynamics. We provide evidence that one or more RCC1 repeat genes are distributed in two main clusters of L. pneumophila strains and have divergently evolved to target different components of the Ran GTPase activation cycle at different subcellular sites. Thus, L. pneumophila employs a sophisticated strategy to subvert host cell Ran GTPase during infection.

Details

Language :
English
ISSN :
21612129 and 21507511
Database :
OpenAIRE
Journal :
mBio, mBio, American Society for Microbiology, 2020, 11 (2), pp.e00405-20. ⟨10.1128/mBio.00405-20⟩, mBio, Vol 11, Iss 2, p e00405-20 (2020), mBio, 2020, 11 (2), pp.e00405-20. ⟨10.1128/mBio.00405-20⟩, mBio, Vol 11, Iss 2 (2020)
Accession number :
edsair.dedup.wf.001..687ee4c504643f1f703e2fc7885119da
Full Text :
https://doi.org/10.1128/mBio.00405-20⟩