Cargando…
LRRK2 functions as a Wnt signaling scaffold, bridging cytosolic proteins and membrane-localized LRP6
Mutations in PARK8, encoding leucine-rich repeat kinase 2 (LRRK2), are a frequent cause of Parkinson's disease (PD). Nonetheless, the physiological role of LRRK2 remains unclear. Here, we demonstrate that LRRK2 participates in canonical Wnt signaling as a scaffold. LRRK2 interacts with key Wnt...
Autores principales: | Berwick, Daniel C., Harvey, Kirsten |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2012
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3709196/ https://www.ncbi.nlm.nih.gov/pubmed/22899650 http://dx.doi.org/10.1093/hmg/dds342 |
Ejemplares similares
-
LRRK2: an éminence grise of Wnt-mediated neurogenesis?
por: Berwick, Daniel C., et al.
Publicado: (2013) -
Protective LRRK2 R1398H Variant Enhances GTPase and Wnt Signaling Activity
por: Nixon-Abell, Jonathon, et al.
Publicado: (2016) -
LRP5 and LRP6 in Wnt Signaling: Similarity and Divergence
por: Ren, Qian, et al.
Publicado: (2021) -
Pathogenic LRRK2 variants are gain-of-function mutations that enhance LRRK2-mediated repression of β-catenin signaling
por: Berwick, Daniel C., et al.
Publicado: (2017) -
Wnt co-receptors Lrp5 and Lrp6 differentially mediate Wnt3a signaling in osteoblasts
por: Sebastian, Aimy, et al.
Publicado: (2017)