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July 4, 2026Nature Communications0 citationsOpen Access

Comparative analysis of Cdc48-dependent proteolysis at the ER, mitochondria and chloroplasts

ALAnne LauSNSreedhar NellaepalliPJPaul Jarvis

Key Points

  • The analysis aims to compare Cdc48-dependent proteolytic systems in different organelles.
  • Conducted a comparative analysis of Cdc48-dependent proteolysis at the endoplasmic reticulum, mitochondria, and chloroplasts.
  • Focused on both similarities and differences in these proteolytic systems across organelles.
  • Identified adaptations of Cdc48-dependent systems to maintain protein homeostasis specific to each organelle.
  • Established that understanding these systems can have implications for human health and agricultural practices.

Abstract

Abstract The ubiquitin-proteasome system (UPS) is the preeminent proteolytic system in eukaryotes. While soluble nucleocytosolic proteins are readily accessed by the UPS, organelle-localised proteins present major, membrane-related accessibility challenges. Cells overcome this problem by employing the conserved AAA+ ATPase Cdc48 to extract organellar proteins to the cytosol, thereby enabling proteasomal degradation. Major Cdc48-dependent proteolytic systems exist at the endoplasmic reticulum, mitochondria and chloroplasts, and are uniquely adapted to deliver protein homeostasis within the respective organelles. We provide a focused comparison of these systems, analysing similarities and differences between them. Better understanding of underlying principles has important implications spanning human health and agriculture.

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Cite This Study

Lau et al. (2026) studied this question.

synapsesocial.com/papers/6a48a36b89561a0c2d78d5eehttps://doi.org/10.1038/s41467-026-74728-z
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