The PI3K and MAPK/p38 pathways control stress granule assembly in a hierarchical manner

Alexander Martin Heberle; Patricia Razquin Navas; Miriam Langelaar-Makkinje; Katharina Kasack; Ahmed Sadik; Erik Faessler; Udo Hahn; Philip Marx-Stoelting; Christiane A Opitz; Christine Sers; Ines Heiland; Sascha Schäuble; Kathrin Thedieck

doi:10.26508/lsa.201800257

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The PI3K and MAPK/p38 pathways control stress granule assembly in a hierarchical manner

Alexander Martin Heberle, Patricia Razquin Navas, Miriam Langelaar-Makkinje, Katharina Kasack, View ORCID ProfileAhmed Sadik, View ORCID ProfileErik Faessler, Udo Hahn, Philip Marx-Stoelting, View ORCID ProfileChristiane A Opitz, View ORCID ProfileChristine Sers, View ORCID ProfileInes Heiland Correspondence email, View ORCID ProfileSascha Schäuble Correspondence email, View ORCID ProfileKathrin Thedieck Correspondence email

Alexander Martin Heberle

1Laboratory of Pediatrics, Section Systems Medicine of Metabolism and Signaling, University of Groningen, University Medical Center Groningen, Groningen, The Netherlands

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Patricia Razquin Navas

1Laboratory of Pediatrics, Section Systems Medicine of Metabolism and Signaling, University of Groningen, University Medical Center Groningen, Groningen, The Netherlands

2Department for Neuroscience, School of Medicine and Health Sciences, Carl von Ossietzky University Oldenburg, Oldenburg, Germany

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Miriam Langelaar-Makkinje

1Laboratory of Pediatrics, Section Systems Medicine of Metabolism and Signaling, University of Groningen, University Medical Center Groningen, Groningen, The Netherlands

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Katharina Kasack

3Laboratory of Molecular Tumor Pathology, Institute of Pathology, Charité Universitätsmedizin Berlin, Berlin, Germany

4German Cancer Consortium (DKTK), Partner Site Berlin, German Cancer Research Center (DKFZ), Heidelberg, Germany

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Ahmed Sadik

5Brain Cancer Metabolism Group, German Cancer Research Center (DKFZ), German Cancer Consortium (DKTK), Heidelberg, Germany

6Faculty of Bioscience, Heidelberg University, Heidelberg, Germany

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Erik Faessler

7Jena University Language and Information Engineering Lab, Friedrich-Schiller-University Jena, Jena, Germany

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Udo Hahn

7Jena University Language and Information Engineering Lab, Friedrich-Schiller-University Jena, Jena, Germany

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Philip Marx-Stoelting

8German Federal Institute for Risk Assessment, Strategies for Toxicological Assessment, Experimental Toxicology and ZEBET, German Centre for the Protection of Laboratory Animals (Bf3R), Berlin, Germany

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Christiane A Opitz

5Brain Cancer Metabolism Group, German Cancer Research Center (DKFZ), German Cancer Consortium (DKTK), Heidelberg, Germany

9Neurology Clinic and National Center for Tumor Diseases, University Hospital of Heidelberg, Heidelberg, Germany

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Christine Sers

3Laboratory of Molecular Tumor Pathology, Institute of Pathology, Charité Universitätsmedizin Berlin, Berlin, Germany

4German Cancer Consortium (DKTK), Partner Site Berlin, German Cancer Research Center (DKFZ), Heidelberg, Germany

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Ines Heiland

10Faculty of Bioscience, Fisheries and Economics, Department of Arctic and Marine Biology, UiT The Arctic University of Norway, Tromsø, Norway

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For correspondence: ines.heiland@uit.no

Sascha Schäuble

7Jena University Language and Information Engineering Lab, Friedrich-Schiller-University Jena, Jena, Germany

11Systems Biology and Bioinformatics, Leibniz Institute for Natural Product Research and Infection Biology, Hans Knöll Institute, Jena, Germany

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For correspondence: sascha.schaeuble@uni-jena.de

Kathrin Thedieck

1Laboratory of Pediatrics, Section Systems Medicine of Metabolism and Signaling, University of Groningen, University Medical Center Groningen, Groningen, The Netherlands

2Department for Neuroscience, School of Medicine and Health Sciences, Carl von Ossietzky University Oldenburg, Oldenburg, Germany

12Institute of Biochemistry and Center for Molecular Biosciences Innsbruck, University of Innsbruck, Innsbruck, Austria

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For correspondence: kathrin.thedieck@uibk.ac.at

Published 28 March 2019. DOI: 10.26508/lsa.201800257

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PI3K and p38 are pro-stress-granule-kinases

Alexander Martin Heberle, Patricia Razquin Navas, Miriam Langelaar-Makkinje, Katharina Kasack, Ahmed Sadik, Erik Faessler, Udo Hahn, Philip Marx-Stoelting, Christiane A Opitz, Christine Sers, Ines Heiland, Sascha Schäuble, Kathrin Thedieck

Life Science Alliance Mar 2019, 2 (2) e201800257; DOI: 10.26508/lsa.201800257

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PI3K and p38 are pro-stress-granule-kinases

Life Science Alliance Mar 2019, 2 (2) e201800257; DOI: 10.26508/lsa.201800257

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