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Resveratrol and related stilbene derivatives induce stress granules with distinct clearance kinetics

Resveratrol and related stilbene derivatives induce stress granules with distinct clearance kinetics
Resveratrol and related stilbene derivatives induce stress granules with distinct clearance kinetics

Stress granules (SGs) are ribonucleoprotein functional condensates that form under stress conditions in all eukaryotic cells. Although their stress-survival function is far from clear, SGs have been implicated in the regulation of many vital cellular pathways. Consequently, SG dysfunction is thought to be a mechanistic point of origin for many neurodegenerative disorders, including amyotrophic lateral sclerosis (ALS). Additionally, SGs are thought to play a role in pathogenic pathways as diverse as viral infection and chemotherapy resistance. There is a growing consensus on the hypothesis that understanding the mechanistic regulation of SG physical properties is essential to understanding their function. Although the internal dynamics and condensation mechanisms of SGs have been broadly investigated, there have been fewer investigations into the timing of SG formation and clearance in live cells. Because the lifetime of SG persistence can be a key factor in their function and tendency toward pathological dysregulation, SG clearance mechanisms deserve particular attention. Here we show that resveratrol and its analogues piceatannol, pterostilbene, and 3,4,5,4'-tetramethoxystilbene induce G3BP-dependent SG formation with atypically rapid clearance kinetics. Resveratrol binds to G3BP, thereby reducing its protein-protein association valency. We suggest that altering G3BP valency is a pathway for the formation of uniquely transient SGs.

Carrier Proteins/metabolism, Cell Line, Tumor, Cytoplasmic Granules/drug effects, DNA Helicases/drug effects, HEK293 Cells, HeLa Cells, Humans, Kinetics, Poly-ADP-Ribose Binding Proteins/drug effects, RNA Helicases/drug effects, RNA Recognition Motif Proteins/drug effects, Resveratrol/pharmacology, Ribonucleoproteins/metabolism, Stress Granules/drug effects
1059-1524
ar18
Amen, Triana
388dc540-e819-4d07-8f1e-ee0f3949a54b
Guihur, Anthony
6cdb4b54-3810-4760-89a9-debf34566ea0
Zelent, Christina
97327770-1f76-412f-a340-6561ec6479ca
Ursache, Robertas
a4d1d0a8-5372-44e0-9224-2df31b67764c
Wilting, Jörg
eed875e7-fc2d-435d-b89c-a3cb52f9c122
Kaganovich, Daniel
ebb13f4e-e925-4aef-88e7-ddc25ef52d8f
Amen, Triana
388dc540-e819-4d07-8f1e-ee0f3949a54b
Guihur, Anthony
6cdb4b54-3810-4760-89a9-debf34566ea0
Zelent, Christina
97327770-1f76-412f-a340-6561ec6479ca
Ursache, Robertas
a4d1d0a8-5372-44e0-9224-2df31b67764c
Wilting, Jörg
eed875e7-fc2d-435d-b89c-a3cb52f9c122
Kaganovich, Daniel
ebb13f4e-e925-4aef-88e7-ddc25ef52d8f

Amen, Triana, Guihur, Anthony, Zelent, Christina, Ursache, Robertas, Wilting, Jörg and Kaganovich, Daniel (2021) Resveratrol and related stilbene derivatives induce stress granules with distinct clearance kinetics. Molecular Biology of the Cell, 32 (21), ar18. (doi:10.1091/mbc.E21-02-0066).

Record type: Article

Abstract

Stress granules (SGs) are ribonucleoprotein functional condensates that form under stress conditions in all eukaryotic cells. Although their stress-survival function is far from clear, SGs have been implicated in the regulation of many vital cellular pathways. Consequently, SG dysfunction is thought to be a mechanistic point of origin for many neurodegenerative disorders, including amyotrophic lateral sclerosis (ALS). Additionally, SGs are thought to play a role in pathogenic pathways as diverse as viral infection and chemotherapy resistance. There is a growing consensus on the hypothesis that understanding the mechanistic regulation of SG physical properties is essential to understanding their function. Although the internal dynamics and condensation mechanisms of SGs have been broadly investigated, there have been fewer investigations into the timing of SG formation and clearance in live cells. Because the lifetime of SG persistence can be a key factor in their function and tendency toward pathological dysregulation, SG clearance mechanisms deserve particular attention. Here we show that resveratrol and its analogues piceatannol, pterostilbene, and 3,4,5,4'-tetramethoxystilbene induce G3BP-dependent SG formation with atypically rapid clearance kinetics. Resveratrol binds to G3BP, thereby reducing its protein-protein association valency. We suggest that altering G3BP valency is a pathway for the formation of uniquely transient SGs.

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More information

e-pub ahead of print date: 14 October 2021
Published date: 1 November 2021
Keywords: Carrier Proteins/metabolism, Cell Line, Tumor, Cytoplasmic Granules/drug effects, DNA Helicases/drug effects, HEK293 Cells, HeLa Cells, Humans, Kinetics, Poly-ADP-Ribose Binding Proteins/drug effects, RNA Helicases/drug effects, RNA Recognition Motif Proteins/drug effects, Resveratrol/pharmacology, Ribonucleoproteins/metabolism, Stress Granules/drug effects

Identifiers

Local EPrints ID: 482134
URI: http://eprints.soton.ac.uk/id/eprint/482134
ISSN: 1059-1524
PURE UUID: ddd0f1d6-8afc-4a99-bcb3-9a3631829344
ORCID for Triana Amen: ORCID iD orcid.org/0000-0003-4808-7806
ORCID for Daniel Kaganovich: ORCID iD orcid.org/0000-0003-2398-1596

Catalogue record

Date deposited: 19 Sep 2023 17:13
Last modified: 17 Mar 2024 04:22

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Contributors

Author: Triana Amen ORCID iD
Author: Anthony Guihur
Author: Christina Zelent
Author: Robertas Ursache
Author: Jörg Wilting
Author: Daniel Kaganovich ORCID iD

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