TY - JOUR
T1 - Inhibition of NF-κB activation by arsenite through reaction with a critical cysteine in the activation loop of IκB kinase
AU - Kapahi, P.
AU - Takahashi, T.
AU - Natoli, G.
AU - Adams, S. R.
AU - Chen, Y.
AU - Tsien, R. Y.
AU - Karin, M.
PY - 2000/11/17
Y1 - 2000/11/17
N2 - Arsenite is a potent environmental toxin that causes various pathologies including cancers and skin disorders. Arsenite is believed to exert its biological effects through reaction with exposed sulfhydryl groups, especially pairs of adjacent thiols. Here, we describe the mechanism by which arsenite affects the NF-κB signaling pathway. Activation of transcription factor NF-κB depends on the integrity of the IκB kinase (IKK) complex. We found that arsenite potently inhibits NF-κB and IKK activation by binding to Cys-179 in the activation loop of the IKK catalytic subunits, IKKα/β. The affinity of IKKβ for trivalent arsenic was verified in vitro by the ability of IKKβ to enhance the fluorescence of an arsenic-substituted fluorescein dye. The addition of 1,2-dithiol antidotes or replacement of Cys-179 with an alanine residue abolished dye binding to and arsenite inhibition of IKKβ. Overexpression of IKKβ (C179A) protects NF-κB from inhibition by arsenite, indicating that despite the involvement of a large number of distinct gene products in this activation pathway, the critical target for inhibition by arsenite is on the IKK catalytic subunits.
AB - Arsenite is a potent environmental toxin that causes various pathologies including cancers and skin disorders. Arsenite is believed to exert its biological effects through reaction with exposed sulfhydryl groups, especially pairs of adjacent thiols. Here, we describe the mechanism by which arsenite affects the NF-κB signaling pathway. Activation of transcription factor NF-κB depends on the integrity of the IκB kinase (IKK) complex. We found that arsenite potently inhibits NF-κB and IKK activation by binding to Cys-179 in the activation loop of the IKK catalytic subunits, IKKα/β. The affinity of IKKβ for trivalent arsenic was verified in vitro by the ability of IKKβ to enhance the fluorescence of an arsenic-substituted fluorescein dye. The addition of 1,2-dithiol antidotes or replacement of Cys-179 with an alanine residue abolished dye binding to and arsenite inhibition of IKKβ. Overexpression of IKKβ (C179A) protects NF-κB from inhibition by arsenite, indicating that despite the involvement of a large number of distinct gene products in this activation pathway, the critical target for inhibition by arsenite is on the IKK catalytic subunits.
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U2 - 10.1074/jbc.M007204200
DO - 10.1074/jbc.M007204200
M3 - Article
C2 - 10967126
AN - SCOPUS:0034680928
VL - 275
SP - 36062
EP - 36066
JO - Journal of Biological Chemistry
JF - Journal of Biological Chemistry
SN - 0021-9258
IS - 46
ER -