Skip to main content
. 2021 Dec 22;65(7):913–923. doi: 10.1042/EBC20210036

Table 1. Potential roles for cPINK1 in mediating cellular proteostasis.

Proteostasis activity Mechanism Model system References
Transcription cPINK1 nuclear localisation promoted by monoubiquitination; implicated in phosphorylation of transcriptional regulators Overexpressed ΔM104PINK1-EGFP in HeLa, HEK293T, SHSY5Y; siRNA PINK1 knockdown in HEK293 [22,23]
Translation cPINK1-induced phosphorylation at Ser398 of the translation elongation factor eEF1A1 Overexpressed tagged cPINK1 in AD293 [21]
Trafficking Trafficking of mitochondria, including within dendrites and axons, via interaction of cPINK1 with Miro/Milton or PKA Expression of ∆MTS-Pink1 in HEK293-FT, COS7; overexpression of PINK1 in SHSY5Y, PINK1−/− primary cortical neurons; Drosophila [24–26]
Aggregation Direct K-48 ubiquitinated proteins to aggresomes via cPINK1-mediated phosphorylation of SQSTM1 Overexpressed tagged cPINK1 in AD293 [27]
Degradation Sensor of proteasome capacity via cPINK1 accumulation; enhances autophagy during proteasome inhibition MG132 proteasome inhibition [23,27]
Promotes α-syn degradation through autophagy via direct interaction with cPINK1 KD Overexpression of truncated PINK1 variants in HEK293T [28]