PINK1 activation–turning on a promiscuous kinase

Author:

Aerts Liesbeth12,De Strooper Bart13,Morais Vanessa A.12

Affiliation:

1. Center for Human Genetics, LIND and KU Leuven, O&N1 Herestraat 49 box 602, 3000 Leuven, Belgium

2. VIB Center for the Biology of Disease, LIND and KU Leuven, O&N1 Herestraat 49 box 602, 3000 Leuven, Belgium

3. University College London, Institute of Neurology, Queen Square, London WC1N 3BG, U.K.

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.

Publisher

Portland Press Ltd.

Subject

Biochemistry

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