The Inhibitor Endosidin 4 Targets SEC7 Domain-Type ARF GTPase Exchange Factors and Interferes with Subcellular Trafficking in Eukaryotes

Investor logo

Warning

This publication doesn't include Faculty of Sports Studies. It includes Central European Institute of Technology. Official publication website can be found on muni.cz.
Authors

KANIA U. NODZYNSKI Tomasz LU Q. HICKS G.R. NERINCKX W. MISHEV K. PEUROIS F. CHERFILS J. DE RYCKE R. GRONES P. ROBERT S. RUSSINOVA E. FRIML J.

Year of publication 2018
Type Article in Periodical
Magazine / Source Plant Cell
MU Faculty or unit

Central European Institute of Technology

Citation
Web https://academic.oup.com/plcell/article/30/10/2553/6099476?login=true
Doi http://dx.doi.org/10.1105/tpc.18.00127
Keywords GUANINE-NUCLEOTIDE-EXCHANGE; ADP-RIBOSYLATION FACTOR-1; AUXIN EFFLUX CARRIER; TRANS-GOLGI NETWORK; ENDOPLASMIC-RETICULUM; YEAST GOLGI; ARABIDOPSIS-THALIANA; ROOT GRAVITROPISM; BREFELDIN-A; INDUCED HAPLOINSUFFICIENCY
Description The trafficking of subcellular cargos in eukaryotic cells crucially depends on vesicle budding, a process mediated by ARFGEFs (ADP-ribosylation factor guanine nucleotide exchange factors). In plants, ARF-GEFs play essential roles in endocytosis, vacuolar trafficking, recycling, secretion, and polar trafficking. Moreover, they are important for plant development, mainly through controlling the polar subcellular localization of PIN-FORMED transporters of the plant hormone auxin. Here, using a chemical genetics screen in Arabidopsis thaliana, we identified Endosidin 4 (ES4), an inhibitor of eukaryotic ARF-GEFs. ES4 acts similarly to and synergistically with the established ARF-GEF inhibitor Brefeldin A and has broad effects on intracellular trafficking, including endocytosis, exocytosis, and vacuolar targeting. Additionally, Arabidopsis and yeast (Saccharomyces cerevisiae) mutants defective in ARF-GEF show altered sensitivity to ES4. ES4 interferes with the activation-based membrane association of the ARF1 GTPases, but not of their mutant variants that are activated independently of ARF-GEF activity. Biochemical approaches and docking simulations confirmed that ES4 specifically targets the SEC7 domain-containing ARF-GEFs. These observations collectively identify ES4 as a chemical tool enabling the study of ARF-GEF-mediated processes, including ARF-GEF-mediated plant development.
Related projects:

You are running an old browser version. We recommend updating your browser to its latest version.

More info