Serine-ubiquitination regulates Golgi morphology and the secretory pathway upon Legionella infection

  • SidE family of Legionella effectors catalyze non-canonical phosphoribosyl-linked ubiquitination (PR-ubiquitination) of host proteins during bacterial infection. SdeA localizes predominantly to ER and partially to the Golgi apparatus, and mediates serine ubiquitination of multiple ER and Golgi proteins. Here we show that SdeA causes disruption of Golgi integrity due to its ubiquitin ligase activity. The Golgi linking proteins GRASP55 and GRASP65 are PR-ubiquitinated on multiple serine residues, thus preventing their ability to cluster and form oligomeric structures. In addition, we found that the functional consequence of Golgi disruption is not linked to the recruitment of Golgi membranes to the growing Legionella-containing vacuoles. Instead, it affects the host secretory pathway. Taken together, our study sheds light on the Golgi manipulation strategy by which Legionella hijacks the secretory pathway and promotes bacterial infection.
Metadaten
Author:Yaobin Liu, Rukmini MukherjeeORCiD, Florian Bonn, Thomas Colby, Ivan MatićORCiDGND, Marius Glogger, Mike HeilemannORCiDGND, Ivan ĐikićORCiDGND
URN:urn:nbn:de:hebis:30:3-628034
DOI:https://doi.org/10.1038/s41418-021-00830-y
ISSN:1476-5403
Parent Title (English):Cell death and differentiation
Publisher:Macmillan
Place of publication:London
Document Type:Article
Language:English
Date of Publication (online):2021/07/20
Date of first Publication:2021/07/20
Publishing Institution:Universitätsbibliothek Johann Christian Senckenberg
Release Date:2022/06/07
Tag:Biochemistry; Cell biology
Volume:28
Issue:10
Page Number:13
First Page:2957
Last Page:2969
Note:
This project was funded by European Research Council (ERC) under the European Union’s Horizon 2020 research and innovation programme (ID, grant agreement No 742720), and LOEWE Main Research Focus DynaMem of the German Federal State of Hesse (III L6-519/03/03.001-(O006), to ID). Work in Ivan Matic’s laboratory was funded by the Deutsche Forschungsgemeinschaft (DFG, German Research Foundation) under Germany’s Excellence Strategy-CECAD, EXC 2030-390661388 (to IM), and the EMBO Young Investigator Programme (to IM). MH and MG acknowledge funding by the Deutsche Forschungsgemeinschaft (DFG, German Research Foundation)—Project-ID 253130777—SFB 1177. Open Access funding enabled and organized by Projekt DEAL
HeBIS-PPN:495777498
Institutes:Biochemie, Chemie und Pharmazie
Medizin
Fachübergreifende Einrichtungen / Buchmann Institut für Molekulare Lebenswissenschaften (BMLS)
Dewey Decimal Classification:5 Naturwissenschaften und Mathematik / 57 Biowissenschaften; Biologie / 570 Biowissenschaften; Biologie
6 Technik, Medizin, angewandte Wissenschaften / 61 Medizin und Gesundheit / 610 Medizin und Gesundheit
Sammlungen:Universitätspublikationen
Licence (German):License LogoCreative Commons - Namensnennung 4.0