The actin and Rho‐modifying toxins PTC3 and PTC5 of Photorhabdus luminescens: enzyme characterization and induction of MAL/SRF‐dependent transcription. (22nd November 2014)

• Record Type: Journal Article
• Authors: Pfaumann, Vanda; Lang, Alexander E.; Schwan, Carsten; Schmidt, Gudula; Aktories, Klaus
• Is Part Of: Cellular microbiology. Volume 17:Number 4(2015:Apr.)
• Page Start: 579
• Page End: 594
• Publication Date: 2014-11-22
• Subjects: Microbiology -- Periodicals; Cytology -- Periodicals; Host-parasite relationships -- Periodicals; Microbiology -- Periodicals; Cells -- Periodicals; Microbiologie -- Périodiques; Microbiologie; Relation hôte-parasite; Cytologie; Cellule; Réponse cellulaire; Ressource Internet (Descripteur de forme); Périodique électronique (Descripteur de forme); 579.05
• DOI: 10.1111/cmi.12386
• Languages: English
• ISSNs: 1462-5814

Abstract

<abstract abstract-type="main"> <title>Summary</title> <p>PTC3 and PTC5 are tripartite Tc (toxin complex) toxins from <italic>P</italic><italic>hotorhabdus luminescens</italic>, which consist of the binding component TcdA1, the linker component TcdB2 and the enzyme components TccC3 and TccC5 respectively. While PTC5 adenosine diphosphate (ADP)‐ribosylates Rho proteins at Gln61/63 resulting in constitutive activation of the GTPases, PTC3 ADP‐ribosylates actin at Thr148 thereby inducing actin polymerization. Here, we identified amino acids involved in ADP‐ribosyltransferase activity of TccC3 and TccC5 and analysed the substrate specificity of Rho‐activating TccC5. We compared the time dependency of Rho protein activation by PTC5 in HeLa cells with the effects of <italic>E</italic><italic>scherichia coli</italic> cytotoxic necrotizing factor 1, which activates Rho GTPases by deamidation of Gln61/63. Using a luciferase reporter assay, we show that PTC5 and PTC3 stimulated gene transcription via myocardin‐related transcription factor A (also called MAL) and AP1. MAL activation by PTC5 involved Rho kinase and formins. Activation of AP1 by PTC5 occurred via two MAP kinase pathways involving extracellular signal‐regulated kinase and Jun kinase respectively.</p> </abstract>