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KLHL12 Promotes Non-Lysine Ubiquitination of the Dopamine Receptors D(4.2) and D(4.4), but Not of the ADHD-Associated D(4.7) Variant

DOPAMINE D4 RECEPTOR POLYMORPHISM: The dopamine D(4) receptor has an important polymorphism in its third intracellular loop that is intensively studied and has been associated with several abnormal conditions, among others, attention deficit hyperactivity disorder. KLHL12 PROMOTES UBIQUITINATION OF...

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Detalles Bibliográficos
Autores principales: Skieterska, Kamila, Rondou, Pieter, Lintermans, Béatrice, Van Craenenbroeck, Kathleen
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4738440/
https://www.ncbi.nlm.nih.gov/pubmed/26717573
http://dx.doi.org/10.1371/journal.pone.0145654
Descripción
Sumario:DOPAMINE D4 RECEPTOR POLYMORPHISM: The dopamine D(4) receptor has an important polymorphism in its third intracellular loop that is intensively studied and has been associated with several abnormal conditions, among others, attention deficit hyperactivity disorder. KLHL12 PROMOTES UBIQUITINATION OF THE DOPAMINE D4 RECEPTOR ON NON-LYSINE RESIDUES: In previous studies we have shown that KLHL12, a BTB-Kelch protein, specifically interacts with the polymorphic repeats of the dopamine D(4) receptor and enhances its ubiquitination, which, however, has no influence on receptor degradation. In this study we provide evidence that KLHL12 promotes ubiquitination of the dopamine D(4) receptor on non-lysine residues. By using lysine-deficient receptor mutants and chemical approaches we concluded that ubiquitination on cysteine, serine and/or threonine is possible. DIFFERENTIAL UBIQUITINATION OF THE DOPAMINE D4 RECEPTOR POLYMORPHIC VARIANTS: Additionally, we show that the dopamine D(4.7) receptor variant, which is associated with a predisposition to develop attention deficient hyperactivity disorder, is differentially ubiquitinated compared to the other common receptor variants D(4.2) and D(4.4). Together, our study suggests that GPCR ubiquitination is a complex and variable process.