Death by ribosome

The ribotoxic stress response (RSR) surveils elongating ribosomes and responds to a multitude of translational aberrations.In the RSR, the sensing kinase ZAKα, once activated, signals toward activation of the stress-associated mitogen-activated protein (MAP)-kinases p38 and jun N-terminal kinase (JN...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Trends in cell biology 2024-12
Hauptverfasser: Vind, Anna Constance, Zhong, Franklin L., Bekker-Jensen, Simon
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
Beschreibung
Zusammenfassung:The ribotoxic stress response (RSR) surveils elongating ribosomes and responds to a multitude of translational aberrations.In the RSR, the sensing kinase ZAKα, once activated, signals toward activation of the stress-associated mitogen-activated protein (MAP)-kinases p38 and jun N-terminal kinase (JNK).RSR activation mediates cell death by JNK-dependent apoptosis and p38-dependent pyroptosis.Next to exogenous/endogenous stress signals and plant and microbial toxins, ribotoxicity and RSR activation may be caused by cell-intrinsic factors. Next to their essential role as protein production factories, ribosomes serve as molecular sensors of cell stress. Stalled and collided ribosomes trigger specific stress signaling, including the ribotoxic stress response (RSR). The RSR is initiated by the mitogen-activated protein (MAP)-3 kinase ZAKα in response to a plethora of translational aberrations, leading to activation of the stress-activated MAP kinases p38 and jun N-terminal kinase (JNK). Recent insights have highlighted an important role for the RSR pathway in triggering programmed cell death processes, including apoptosis and pyroptosis, in a broad range of physiologically relevant conditions. In this review, we summarize recent work on known links between programmed and accidental ribosome toxicity, RSR signaling, and cell death. Next to their essential role as protein production factories, ribosomes serve as molecular sensors of cell stress. Stalled and collided ribosomes trigger specific stress signaling, including the ribotoxic stress response (RSR). The RSR is initiated by the mitogen-activated protein (MAP)-3 kinase ZAKα in response to a plethora of translational aberrations, leading to activation of the stress-activated MAP kinases p38 and jun N-terminal kinase (JNK). Recent insights have highlighted an important role for the RSR pathway in triggering programmed cell death processes, including apoptosis and pyroptosis, in a broad range of physiologically relevant conditions. In this review, we summarize recent work on known links between programmed and accidental ribosome toxicity, RSR signaling, and cell death.
ISSN:0962-8924
1879-3088
1879-3088
DOI:10.1016/j.tcb.2024.10.013