Stalling the stress response: chronic low-level stress inhibits stress granule formation via translation elongation impairment.
New post from Mohammed Jalloh #UniversityofArizona highlighting work from the Ivanov lab. #preprint
#preLight β¬οΈπ
https://prelights.biologists.com/highlights/chronic-stress-antagonizes-formation-of-stress-granules/
#biology #preprint #stress #StressGranules #translation #biochemistry

Chronic stress antagonizes formation of Stress Granules - preLights
Stalling the stress response: chronic low-level stress inhibits stress granule formation via translation elongation impairment
preLightsA very nice review on RNA granules from Geraldine Seydoux's lab at Genes & Development.
"RNA granules: functional compartments or incidental condensates?"
#RNA #granules #mRNA #phaseseparation #translation #splicing #Pbodies #StressGranules
#GermGranules
https://genesdev.cshlp.org/content/37/9-10/354.abstract
RNA granules: functional compartments or incidental condensates?
A biweekly scientific journal publishing high-quality research in molecular biology and genetics, cancer biology, biochemistry, and related fields
In EMBO Journal issue 3:
Host #mucins negotiate peace with #toxigenic #Vibrio
Cytosolic #stressgranules relieve nuclear #ubiquitin-#proteasome system
#Smoothened #cholesterylation and ER exit links in #Hedgehog signaling
Developmental #cellfate decision control by #chromatin reader #TRIM33
Cover by Kimon Lemonides, Helen Walden et al
https://www.embopress.org/toc/14602075/2023/42/3
LSI Paper of the DayβοΈ
Dr. Jibin Sadasivan and a team from the Eric Jan Lab provide new insights into how viruses manipulate the formation of stress granules - a potential strategy for protecting viral proteins and RNA and promoting infection in a new @PLOS Pathogens study.
https://journals.plos.org/plospathogens/article?id=10.1371/journal.ppat.1010598#ack
#infection #inflammation #stressgranules


Targeting Nup358/RanBP2 by a viral protein disrupts stress granule formation
Author summary Viruses often inhibit a cellular stress response that leads to the accumulation of RNA and protein condensates called stress granules. How this occurs and why this would benefit virus infection are not fully understood. Here, we reveal a viral protein that can block stress granules and identify a key amino acid residue in the protein that inactivates this function. We demonstrate that this viral protein has multiple functions to modulate nuclear events including mRNA export and transcription to regulate stress granule formation. We identify a key host protein that is important for viral protein-mediated stress granule inhibition, thus providing mechanistic insights. This study reveals a novel viral strategy in modulating stress granule formation to promote virus infection.
What happens to the
#ubiquitin-
#proteasome system in cells that cannot form
#stressgranules?
Nico Dantuma & coworkers at Karolinska Institute find surprising
#nucleolar relocalization of DRiP
#peptides, compromising
#proteostasis in the nucleus
https://www.embopress.org/doi/10.15252/embj.2022111802
RNA granule for translation quality control in Saccharomyces cerevisiae
Cytoplasmic RNA granules compartmentalize phases of the translation cycle in eukaryotes. We previously reported the localization of oxidized RNA to cytoplasmic foci called oxidized RNA bodies (ORBs) in human cells. We show here that ORBs are RNA granules in Saccharomyces cerevisiae. Several lines of evidence support a role of ORBs in the compartmentalization of no-go decay and ribosome quality control, the translation quality control pathways that recognize and clear aberrant mRNAs, including those with oxidized bases. Translation is required by these pathways and ORBs. Translation quality control factors localize to ORBs. A substrate of translation quality control, a stalled mRNA-ribosome-nascent chain complex, localizes to ORBS. Translation quality control mutants have altered ORB numbers, sizes, or both. In addition, we identify 68 ORB proteins, by immunofluorescence staining directed by proteomics, which further support their role in translation quality control and reveal candidate new factors for these pathways.
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