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| Main Authors: | , , , , , |
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| Format: | Artículo Open Access |
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Wiley
2026
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| Online Access: | https://febs.onlinelibrary.wiley.com/doi/10.1111/febs.70607 |
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| author | Paulina Czechowicz Anna Więch‐Walów Sylwia Kozioł Jakub Dudzik James F. Collawn Rafal Bartoszewski |
| author_facet | Paulina Czechowicz Anna Więch‐Walów Sylwia Kozioł Jakub Dudzik James F. Collawn Rafal Bartoszewski Paulina Czechowicz Anna Więch‐Walów Sylwia Kozioł Jakub Dudzik James F. Collawn Rafal Bartoszewski |
| collection | Wiley Open Access |
| contents | A multilayered stress‐response circuit: The mammalian mitochondrial UPR Paulina Czechowicz Anna Więch‐Walów Sylwia Kozioł Jakub Dudzik James F. Collawn Rafal Bartoszewski The FEBS Journal Mitochondrial proteotoxic stress activates the mammalian UPR mt through a multilayered mechanistic architecture rather than a linear pathway. At its core lies an import‐gated sensing logic: reduced preprotein import and mito–nuclear stoichiometric imbalance activates the integrated stress response (ISR) toward the translation of ATF4, CHOP, and the mitochondria‐targeted transcription factor ATF5. These factors cooperatively reprogram transcription to expand the chaperone–protease capacity while transiently reducing the nuclear‐encoded OXPHOS load. Parallel translational mechanisms that include eIF2α‐dependent repression, stress‐granule triage, and miRNA‐driven selective silencing reduce the mitochondrial precursor import and maintain proteostatic symmetry between the cytosol and mitochondria. Within the organelle, LONP1‐ and CLPP‐dependent proteolysis, mitoribosome pausing, and tRNA‐processing checkpoints further dampen nascent chain pressure. Epigenetic licensing by demethylases and acetyltransferases links metabolic and bioenergetic status to promoter accessibility at UPR mt loci. Together, these import‐gated, translational, and epigenetic control layers form a coherent mechanistic circuit ensuring that mitochondrial recovery is matched to folding, assembly, and metabolic capacity. We propose a unified framework explaining how these layers cooperate to determine adaptive versus maladaptive outcomes. 10.1111/febs.70607 http://onlinelibrary.wiley.com/termsAndConditions#vor |
| doi_str_mv | 10.1111/febs.70607 |
| format | Artículo Open Access |
| id | wiley_oa_10_1111_febs_70607 |
| institution | Wiley Open Access |
| license_str_mv | http://onlinelibrary.wiley.com/termsAndConditions#vor |
| publishDate | 2026 |
| publisher | Wiley |
| record_format | wiley_oa |
| spellingShingle | A multilayered stress‐response circuit: The mammalian mitochondrial UPR Paulina Czechowicz Anna Więch‐Walów Sylwia Kozioł Jakub Dudzik James F. Collawn Rafal Bartoszewski The FEBS Journal A multilayered stress‐response circuit: The mammalian mitochondrial UPR Paulina Czechowicz Anna Więch‐Walów Sylwia Kozioł Jakub Dudzik James F. Collawn Rafal Bartoszewski The FEBS Journal Mitochondrial proteotoxic stress activates the mammalian UPR mt through a multilayered mechanistic architecture rather than a linear pathway. At its core lies an import‐gated sensing logic: reduced preprotein import and mito–nuclear stoichiometric imbalance activates the integrated stress response (ISR) toward the translation of ATF4, CHOP, and the mitochondria‐targeted transcription factor ATF5. These factors cooperatively reprogram transcription to expand the chaperone–protease capacity while transiently reducing the nuclear‐encoded OXPHOS load. Parallel translational mechanisms that include eIF2α‐dependent repression, stress‐granule triage, and miRNA‐driven selective silencing reduce the mitochondrial precursor import and maintain proteostatic symmetry between the cytosol and mitochondria. Within the organelle, LONP1‐ and CLPP‐dependent proteolysis, mitoribosome pausing, and tRNA‐processing checkpoints further dampen nascent chain pressure. Epigenetic licensing by demethylases and acetyltransferases links metabolic and bioenergetic status to promoter accessibility at UPR mt loci. Together, these import‐gated, translational, and epigenetic control layers form a coherent mechanistic circuit ensuring that mitochondrial recovery is matched to folding, assembly, and metabolic capacity. We propose a unified framework explaining how these layers cooperate to determine adaptive versus maladaptive outcomes. 10.1111/febs.70607 http://onlinelibrary.wiley.com/termsAndConditions#vor |
| title | A multilayered stress‐response circuit: The mammalian mitochondrial UPR |
| topic | The FEBS Journal |
| url | https://febs.onlinelibrary.wiley.com/doi/10.1111/febs.70607 |