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Updated: Apr 20, 2026

Methods to Classify Cytoplasmic Foci as Mammalian Stress Granules
Published on: May 12, 2017
Granules harboring translationally active mRNAs provide a platform for P-body formation following stress
Jennifer Lui1, Lydia M Castelli1, Mariavittoria Pizzinga1
1Faculty of Life Sciences, Michael Smith Building, The University of Manchester, Oxford Road, Manchester M13 9PT, UK.
Abstract:
The localization of mRNA to defined cytoplasmic sites in eukaryotic cells not only allows localized protein production but also determines the fate of mRNAs. For instance, translationally repressed mRNAs localize to P-bodies and stress granules where their decay and storage, respectively, are directed. Here, we find that several mRNAs are localized to granules in unstressed, actively growing cells. These granules play a key role in the stress-dependent formation of P-bodies. Specific glycolytic mRNAs are colocalized in multiple granules per cell, which aggregate during P-body formation. Such aggregation is still observed under conditions or in mutants where P-bodies do not form. In unstressed cells, the mRNA granules appear associated with active translation; this might enable a coregulation of protein expression from the same pathways or complexes. Parallels can be drawn between this coregulation and the advantage of operons in prokaryotic systems.
Insights
In unstressed cells, specific mRNAs form granules, aiding stress granule and P-body formation. These mRNA granules may coregulate protein expression, similar to prokaryotic operons.
Area of Science:
- Cell Biology
- Molecular Biology
- Gene Expression
Background:
- Messenger RNA (mRNA) localization directs protein production and influences mRNA fate in eukaryotic cells.
- Translationally repressed mRNAs are found in P-bodies (for decay) and stress granules (for storage).
Purpose of the Study:
- To investigate the role and characteristics of mRNA granules in unstressed, actively growing cells.
- To understand the relationship between these granules and the formation of P-bodies and stress granules.
Main Methods:
- Microscopy techniques to visualize mRNA localization and granule formation.
- Analysis of mRNA colocalization within granules.
- Investigation of granule behavior in different cellular conditions and mutant strains.
Main Results:
- Several mRNAs localize to distinct granules in unstressed cells.
- These granules are crucial for the stress-induced formation of P-bodies.
- Specific glycolytic mRNAs colocalize in multiple granules per cell and aggregate during P-body formation.
- Granule aggregation occurs even when P-bodies do not form.
- In unstressed cells, mRNA granules are associated with active translation.
Conclusions:
- mRNA granules in unstressed cells play a role in stress-dependent P-body formation.
- The colocalization and aggregation of specific mRNAs in granules suggest a mechanism for coregulating protein expression.
- This coregulation parallels the functional advantages of operons in prokaryotes.
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