Structural and Functional Characterization of Nrf2 Degradation by the Glycogen Synthase Kinase 3/β-TrCP Axis

التفاصيل البيبلوغرافية
العنوان: Structural and Functional Characterization of Nrf2 Degradation by the Glycogen Synthase Kinase 3/β-TrCP Axis
المؤلفون: Patricia Rada, Ana I. Rojo, Nathalie Evrard-Todeschi, Nadia G. Innamorato, Axelle Cotte, Tomasz Jaworski, Julio C. Tobón-Velasco, Herman Devijver, María Flor García-Mayoral, Fred Van Leuven, John D. Hayes, Gildas Bertho, Antonio Cuadrado
المساهمون: UAM. Departamento de Bioquímica
المصدر: Biblos-e Archivo. Repositorio Institucional de la UAM
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بيانات النشر: Informa UK Limited, 2012.
سنة النشر: 2012
مصطلحات موضوعية: Male, Models, Molecular, Cell signaling, NF-E2-Related Factor 2, Medicina, Beta-Transducin Repeat-Containing Proteins, Molecular Sequence Data, environment and public health, transcription factor Nrf2, Mice, Glycogen Synthase Kinase 3, GSK-3, Serine, Animals, Humans, Amino Acid Sequence, Phosphorylation, Molecular Biology, Peptide sequence, Transcription factor, Cells, Cultured, Mice, Knockout, Glycogen Synthase Kinase 3 beta, biology, Articles, Cell Biology, respiratory system, beta-Transducin Repeat-Containing Proteins, Protein Structure, Tertiary, Ubiquitin ligase, Mice, Inbred C57BL, HEK293 Cells, Biochemistry, Mutagenesis, Mutagenesis, Site-Directed, biology.protein, Signal transduction
الوصف: The transcription factor NF-E2-related factor 2 (Nrf2) is a master regulator of a genetic program, termed the phase 2 response, that controls redox homeostasis and participates in multiple aspects of physiology and pathology. Nrf2 protein stability is regulated by two E3 ubiquitin ligase adaptors, Keap1 and β-TrCP, the latter of which was only recently reported. Here, two-dimensional (2D) gel electrophoresis and site-directed mutagenesis allowed us to identify two serines of Nrf2 that are phosphorylated by glycogen synthase kinase 3β (GSK-3β) in the sequence DSGISL. Nuclear magnetic resonance studies defined key residues of this phosphosequence involved in docking to the WD40 propeller of β-TrCP, through electrostatic and hydrophobic interactions. We also identified three arginine residues of β-TrCP that participate in Nrf2 docking. Intraperitoneal injection of the GSK-3 inhibitor SB216763 led to increased Nrf2 and heme oxygenase-1 levels in liver and hippocampus. Moreover, mice with hippocampal absence of GSK-3βexhibited increased levels of Nrf2 and phase 2 gene products, reduced glutathione, and decreased levels of carbonylated proteins and malondialdehyde. This study establishes the structural parameters of the interaction of Nrf2 with the GSK-3/β-TrCP axis and its functional relevance in the regulation of Nrf2 by the signaling pathways that impinge on GSK-3
This work was supported by MICINN grant SAF2010-18722 from the Spanish Ministry of Science and Innovation. Patricia Rada is contracted under the Formación de Profesorado Universitario program of the Spanish Ministry of Science and Innovation. We acknowledge funding and infrastructural support from EEC 7th Framework Program, KU Leuven Research Fund, and KU Leuven Research & Development
وصف الملف: application/pdf
تدمد: 1098-5549
2010-1872
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fbfe319bf84745853a3bc5708dbf1498Test
https://doi.org/10.1128/mcb.00180-12Test
حقوق: OPEN
رقم الانضمام: edsair.doi.dedup.....fbfe319bf84745853a3bc5708dbf1498
قاعدة البيانات: OpenAIRE