4.2 Article Proceedings Paper

LRRK2 and the Stress Response: Interaction with MKKs and JNK-Interacting Proteins

期刊

NEURODEGENERATIVE DISEASES
卷 7, 期 1-3, 页码 68-75

出版社

KARGER
DOI: 10.1159/000285509

关键词

MAP kinase; c-jun NH2-terminal kinase; Scaffold proteins; Parkinson's disease; Immunoprecipitation

资金

  1. Alzheimer Association
  2. Michael J. Fox Foundation
  3. NIEHS [ES15567]
  4. NINDS [NS060872]
  5. NATIONAL INSTITUTE OF ENVIRONMENTAL HEALTH SCIENCES [R01ES015567] Funding Source: NIH RePORTER
  6. NATIONAL INSTITUTE OF NEUROLOGICAL DISORDERS AND STROKE [R01NS060872] Funding Source: NIH RePORTER

向作者/读者索取更多资源

Increasing evidence supports a putative link between LRRK2 function and the MAP kinase cascades. We recently demonstrated that LRRK2 binds to MKK6, -3, and -7. Previous studies demonstrated that scaffold proteins are essential in the regulation of subcellular localization of stress kinase complexes. The c-jun NH2-terminal kinase (JNK)-interacting proteins (JIPs) are a group of scaffold proteins that play an important role in the regulation of MAP kinase signaling cascades. JIP1-3 are known to regulate the specificity and localization of the JNK pathway, while JIP4 is a specific scaffolding protein for the p38 pathway. We demonstrate that LRRK2 binds to JIP1-4, and is associated with increased levels of total JIP1, -3, -4, oligomeric JIP and ubiquitinated JIP. These results are consistent with a putative role of LRRK2 in regulating the stress kinase cascade. Copyright (C) 2010 S. Karger AG, Basel

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