Cells must rapidly adapt to environmental fluctuations, including heat stress, to maintain homeostasis and ensure survival. A key adaptive mechanism is transcriptional memory, which enables cells to "remember" prior stress exposure and mount a faster or more controlled transcriptional response upon re-exposure. However, the molecular mechanisms underlying transcriptional memory in the heat shock response (HSR) remain incompletely understood. Here, we investigate the role of the RNA-binding protein Mip6 in regulating transcriptional memory during heat stress in Saccharomyces cerevisiae. Using qRT-PCR and RNA-seq, we demonstrate that prior heat shock exposure dampens the activation of heat-responsive genes upon a second stress, a phenomenon more pronounced in mip6Δ mutants. Our transcriptomic analyses reveal that transcriptional memory predominantly suppresses excessive gene expression changes, fine-tuning stress responses. Moreover, we identify a functional and physical interaction between Mip6 and the histone deacetylase Rpd3, a key regulator of transcriptional memory. Loss of both Mip6 and Rpd3 results in synthetic growth defects under heat stress and misregulation of Msn2/4-dependent transcripts, implicating Mip6 as a novel player in the coordination of chromatin and RNA-binding mechanisms during transcriptional memory. Additionally, we show that transcriptional memory modulates metabolic homeostasis and proteostasis. Collectively, our findings implicate Mip6 in the coordination of transcriptional memory in the HSR and reveal a novel link between the RNA-binding protein Mip6 and the chromatin modifier Rpd3 HDAC in stress adaptation. These insights provide a foundation for further exploration of transcriptional memory mechanisms across diverse stress conditions.
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Evidence ID | Analyze ID | Gene/Complex | Systematic Name/Complex Accession | Qualifier | Gene Ontology Term ID | Gene Ontology Term | Aspect | Annotation Extension | Evidence | Method | Source | Assigned On | Reference |
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Evidence ID | Analyze ID | Gene | Gene Systematic Name | Phenotype | Experiment Type | Experiment Type Category | Mutant Information | Strain Background | Chemical | Details | Reference |
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Evidence ID | Analyze ID | Gene | Gene Systematic Name | Disease Ontology Term | Disease Ontology Term ID | Qualifier | Evidence | Method | Source | Assigned On | Reference |
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Evidence ID | Analyze ID | Regulator | Regulator Systematic Name | Target | Target Systematic Name | Direction | Regulation of | Happens During | Regulator Type | Direction | Regulation Of | Happens During | Method | Evidence | Strain Background | Reference |
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Site | Modification | Modifier | Source | Reference |
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Evidence ID | Analyze ID | Interactor | Interactor Systematic Name | Interactor | Interactor Systematic Name | Allele | Assay | Annotation | Action | Phenotype | SGA score | P-value | Source | Reference | Note |
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Evidence ID | Analyze ID | Interactor | Interactor Systematic Name | Interactor | Interactor Systematic Name | Assay | Annotation | Action | Modification | Source | Reference | Note |
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Complement ID | Locus ID | Gene | Species | Gene ID | Strain background | Direction | Details | Source | Reference |
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Evidence ID | Analyze ID | Dataset | Description | Keywords | Number of Conditions | Reference |
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