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.
Authors
- Onn Brandman (ORCID: https://orcid.org/0000-0002-2084-154X)
- Eduardo Tassoni-Tsuchida (ORCID: https://orcid.org/0000-0001-8062-6027)
- Angel M. Madero (ORCID: https://orcid.org/0000-0002-6238-4658)
- Brian Alford (ORCID: https://orcid.org/0000-0002-3064-1939)
- Magda Zaoralova
- Sebastian Alexander Alfonso
Institutions
- Stanford University (US)
Publication Details
- 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
- Field-Weighted Citation Impact
- 0.00