Antioxidant-Induced INrf2 (Keap1) Tyrosine 85 Phosphorylation Controls the Nuclear Export and Degradation of the INrf2–Cul3–Rbx1 Complex to Allow Normal Nrf2 Activation and Repression

Journal of Cell Science- United Kingdom

doi 10.1242/jcs.097295

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Date

February 15, 2012

Authors

James W. Kaspar

Suryakant K. Niture

Anil K. Jaiswal

Publisher

The Company of Biologists

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Antioxidant-Induced INrf2 (Keap1) Tyrosine 85 Phosphorylation Controls the Nuclear Export and Degradation of the INrf2–Cul3–Rbx1 Complex to Allow Normal Nrf2 Activation and Repression

Journal of Cell Science- United Kingdom

Full Text

Abstract

Categories

Date

Authors

Publisher

Related search

Keap1 Controls Postinduction Repression of the Nrf2-Mediated Antioxidant Response by Escorting Nuclear Export of Nrf2

Antioxidant-Induced Phosphorylation of Tyrosine 486 Leads to Rapid Nuclear Export of Bach1 That Allows Nrf2 to Bind to the Antioxidant Response Element and Activate Defensive Gene Expression

Arsenic Induces NAD(P)H-quinone Oxidoreductase I by Disrupting the Nrf2·Keap1·Cul3 Complex and Recruiting Nrf2·Maf to the Antioxidant Response Element Enhancer

Toll-Like Receptor Signaling Induces Nrf2 Pathway Activation Through P62-Triggered Keap1 Degradation

Keap1-Dependent Proteasomal Degradation of Transcription Factor Nrf2 Contributes to the Negative Regulation of Antioxidant Response Element-Driven Gene Expression

Providing Activation-Induced Cytidine Deaminase (AID) to Nuclear Export Inhibitors. Response To: "Complex Downstream Effects of Nuclear Export Inhibition in B-Cell Lymphomas: A Possible Role for Activation-Induced Cytidine Deaminase"

Keap1 Cysteine 288 as a Potential Target for Diallyl Trisulfide-Induced Nrf2 Activation

Quinone-Induced Activation of Keap1/Nrf2 Signaling by Aspirin Prodrugs Masquerading as Nitric Oxide

Nuclear Import and Export Signals in Control of Nrf2