Nup42 safeguards heat-induced mRNAs from nuclear condensation to support chaperone synthesis

Cells exposed to acute stress selectively express stress-adaptive genes while repressing growth-related genes. Upon heat shock, most pre-existing mRNAs localize to translationally repressed biomolecular condensates. How heat-induced mRNAs evade condensation and remain translationally competent remains unclear. Here, we show that ribosomal protein-coding transcripts preferentially accumulate in condensates during heat shock, whereas heat-induced chaperone mRNAs are selectively excluded and preferentially translated. Using a whole-genome CRISPRi screening platform, Fractionation of Reporter-Seq (FRep-Seq), we identify the nucleoporin Nup42 as the strongest suppressor of heat-induced mRNA condensation. Loss of Nup42 triggers temperature- and transcription-dependent nuclear condensation of chaperone mRNAs, which are exported but remain translationally incompetent, leading to impaired chaperone production and thermosensitivity. Co-transcriptional mRNP packaging is a critical determinant of condensation in the absence of Nup42. Together, our findings reveal a nuclear, translation-independent layer of mRNP solubility control that enables heat shock gene expression.

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Journal
bioRxiv (Cold Spring Harbor Laboratory)
Published
2026-02-11
DOI
https://doi.org/10.64898/2026.02.10.705189
Primary Topic
Heat shock proteins research
Type
article
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article

Nup42 safeguards heat-induced mRNAs from nuclear condensation to support chaperone synthesis

Onn Brandman, Eduardo Tassoni-Tsuchida, Angel M. Madero, Brian Alford et al.
bioRxiv (Cold Spring Harbor Laboratory)
Heat shock proteins research
article

Nup42 safeguards heat-induced mRNAs from nuclear condensation to support chaperone synthesis

Onn Brandman, Eduardo Tassoni-Tsuchida, Angel M. Madero, Brian Alford, Magda Zaoralova, Sebastian Alexander Alfonso
article en

Abstract

Cells exposed to acute stress selectively express stress-adaptive genes while repressing growth-related genes. Upon heat shock, most pre-existing mRNAs localize to translationally repressed biomolecular condensates. How heat-induced mRNAs evade condensation and remain translationally competent remains unclear. Here, we show that ribosomal protein-coding transcripts preferentially accumulate in condensates during heat shock, whereas heat-induced chaperone mRNAs are selectively excluded and preferentially translated. Using a whole-genome CRISPRi screening platform, Fractionation of Reporter-Seq (FRep-Seq), we identify the nucleoporin Nup42 as the strongest suppressor of heat-induced mRNA condensation. Loss of Nup42 triggers temperature- and transcription-dependent nuclear condensation of chaperone mRNAs, which are exported but remain translationally incompetent, leading to impaired chaperone production and thermosensitivity. Co-transcriptional mRNP packaging is a critical determinant of condensation in the absence of Nup42. Together, our findings reveal a nuclear, translation-independent layer of mRNP solubility control that enables heat shock gene expression.

bioRxiv (Cold Spring Harbor Laboratory)
Stanford University (US)
Openalex Percentile: Top 58%
Heat shock proteins research
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