PINK1 activation-turning on a promiscuous kinase

Biochem Soc Trans. 2015 Apr;43(2):280-6. doi: 10.1042/BST20150002.

Abstract

PINK1 [phosphatase and tensin homologue (PTEN)-induced putative kinase 1] is a serine/threonine kinase targeted to mitochondria and implicated in early-onset recessive Parkinson's disease (PD). Through the phosphorylation of its downstream targets, PINK1 regulates multiple mitochondrial processes, including ATP production, stress-response and mitochondrial dynamics and quality control. The orchestration of such a wide array of functions by an individual kinase requires a fine-tuned and versatile regulation of its activity. PINK1 proteolytic processing, trafficking and localization, as well as different post-translational modifications, affect its activity and function. Unravelling the regulatory mechanisms of PINK1 is essential for a full comprehension of its kinase function in health and disease.

Publication types

  • Research Support, Non-U.S. Gov't
  • Review

MeSH terms

  • Adenosine Triphosphate / biosynthesis
  • Humans
  • Mitochondria / metabolism*
  • Mitochondria / pathology
  • Parkinson Disease / genetics
  • Parkinson Disease / metabolism*
  • Parkinson Disease / pathology
  • Phosphorylation
  • Protein Kinases / genetics
  • Protein Kinases / metabolism*
  • Protein Processing, Post-Translational
  • Protein Serine-Threonine Kinases / metabolism
  • Protein Transport / genetics*

Substances

  • Adenosine Triphosphate
  • Protein Kinases
  • PTEN-induced putative kinase
  • Protein Serine-Threonine Kinases