Transcriptome-wide mRNP condensation precedes stress granule formation and excludes new mRNAs

Stress-induced messenger ribonucleoprotein (mRNP) condensation is conserved across eukaryotes, resulting in stress granule formation under intense stresses, yet the mRNA composition and function of these condensates remain unclear. Exposure of ribosome-free mRNA following stress is thought to cause condensation and stress granule formation through mRNA-sequence-dependent interactions, leading to disproportionate condensation of long mRNAs. Here, we show that, by contrast, virtually all mRNAs condense in response to multiple stresses in budding yeast with minor length dependence and often without stress granule formation. New transcripts escape mRNP condensation, enabling their selective translation. Inhibiting translation initiation causes formation of mRNP condensates distinct from stress granules and processing bodies (P bodies), and these translation-initiation-inhibited condensates (TIICs) are omnipresent, even in unstressed cells. Stress-induced mRNAs are excluded from TIICs due to the timing of their expression, indicating determinants of escape that are independent of sequence. Together, our results reveal a previously undetected level of translation-linked molecular organization and stress-responsive regulation.

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Publication Details

Journal
Molecular Cell
Published
2025-11-24
DOI
https://doi.org/10.1016/j.molcel.2025.11.003
Citations
8
Primary Topic
RNA Research and Splicing
Type
article
Field-Weighted Citation Impact
6.45
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article

Transcriptome-wide mRNP condensation precedes stress granule formation and excludes new mRNAs

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Molecular Cell
RNA Research and Splicing
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article

Transcriptome-wide mRNP condensation precedes stress granule formation and excludes new mRNAs

Karen M Velez, Caitlin J Wong Hickernell, Edward W. Wallace, Robert H. Singer, D. Allan Drummond, Jared A.M. Bard, Tobin R. Sosnick, Sneha Paul, Jingyi Fei, Hendrik Glauninger, Edo M. Airoldi, Weihan Li
article en
8 citations

Abstract

Stress-induced messenger ribonucleoprotein (mRNP) condensation is conserved across eukaryotes, resulting in stress granule formation under intense stresses, yet the mRNA composition and function of these condensates remain unclear. Exposure of ribosome-free mRNA following stress is thought to cause condensation and stress granule formation through mRNA-sequence-dependent interactions, leading to disproportionate condensation of long mRNAs. Here, we show that, by contrast, virtually all mRNAs condense in response to multiple stresses in budding yeast with minor length dependence and often without stress granule formation. New transcripts escape mRNP condensation, enabling their selective translation. Inhibiting translation initiation causes formation of mRNP condensates distinct from stress granules and processing bodies (P bodies), and these translation-initiation-inhibited condensates (TIICs) are omnipresent, even in unstressed cells. Stress-induced mRNAs are excluded from TIICs due to the timing of their expression, indicating determinants of escape that are independent of sequence. Together, our results reveal a previously undetected level of translation-linked molecular organization and stress-responsive regulation.

Molecular CellVol. 85(23)
Albert Einstein College of Medicine (US), University of Chicago (US), Temple University (US), Texas A&M University (US)
Openalex Percentile: Top 3%
RNA Research and Splicing
6.45
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