A conformation-dependent hydrophobic degron determines Rab9a-mediated vesicular trafficking
Jun Shirai, Toshiki Takahashi, Hiroyuki Kawahara

TL;DR
This study reveals how a specific unstable region in Rab9a, called a CDH degron, is crucial for proper vesicular trafficking of CI-M6PR, working with the protein quality control system.
Contribution
The discovery of a conformation-dependent hydrophobic degron in Rab9a that regulates its stability and function in vesicular trafficking.
Findings
GDP-bound Rab9a has an extremely short half-life compared to Rab7.
Hydrophobic residues in Rab9a's switch I region form a CDH degron recognized by the PQC machinery.
Valosin-containing protein/p97 is identified as a PQC factor for GDP-bound Rab9a.
Abstract
The small GTPase Rab9 plays a major role in the vesicular trafficking of cation-independent mannose-6-phosphate receptor (CI-M6PR). CI-M6PR trafficking has also been reported to be perturbed by the dysfunction of a ubiquitin ligase necessary for protein quality control (PQC). However, the mechanism underlying the participation of the PQC machinery in CI-M6PR trafficking is poorly understood. In this study, we found an extremely short half-life of GDP-bound Rab9, which is in clear contrast to its phylogenetically closest relative, Rab7. Comparison of the amino acid sequences of these relatives revealed that hydrophobic residues are specifically exposed in the switch I region of Rab9a and that these residues are recognized by the PQC machinery. We defined this exposed hydrophobicity as a conformation-dependent hydrophobic (CDH) degron because its existence determines the instability of…
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Taxonomy
TopicsCellular transport and secretion · Ubiquitin and proteasome pathways · Protein Kinase Regulation and GTPase Signaling
