Jain Abhinav K, Jaiswal Anil K
Department of Pharmacology, Baylor College of Medicine, Houston, Texas 77030, USA.
J Biol Chem. 2007 Jun 1;282(22):16502-10. doi: 10.1074/jbc.M611336200. Epub 2007 Apr 2.
NF-E2-related factor 2 (Nrf2) regulates expression and coordinated induction of a battery of chemoprotective genes in response to oxidative and electrophilic stress. This leads to protection against oxidative stress and neoplastic diseases. Nuclear import and export of Nrf2 play a significant role in control of nuclear levels of Nrf2 and thus the expression of Nrf2 down-stream genes. Tyrosine kinase Fyn phosphorylates tyrosine 568 of Nrf2 that leads to the nuclear export of Nrf2. In this study, we investigated the upstream factor(s) in regulation of Fyn and Fyn-mediated nuclear export of Nrf2. The investigations shed light on a novel mechanism of Nrf2 regulation in response to oxidative stress. We demonstrate that GSK-3beta acts upstream of Fyn kinase in control of nuclear export of Nrf2. Chemical and short interfering RNA-mediated inhibition of GSK-3beta led to nuclear accumulation of Nrf2 and transcriptional activation of the Nrf2 downstream gene nqo1. Chemical and short interfering RNA inhibition of GSK-3beta and Fyn individually and in combination revealed that both kinases follow the same pathway to regulate nuclear export of Nrf2. We further demonstrate that hydrogen peroxide phosphorylates tyrosine 216 of GSK-3beta. This leads to activation of GSK-3beta. The activated GSK-3beta phosphorylates Fyn at threonine residue(s). Phosphorylated Fyn accumulates in the nucleus and phosphorylates Nrf2 at tyrosine 568. This leads to nuclear export, ubiquitination, and degradation of Nrf2.
NF-E2相关因子2(Nrf2)可调节一系列化学保护基因的表达并在氧化应激和亲电应激反应中协调诱导这些基因。这会带来对氧化应激和肿瘤疾病的保护作用。Nrf2的核输入和输出在控制Nrf2的核水平以及Nrf2下游基因的表达方面发挥着重要作用。酪氨酸激酶Fyn使Nrf2的酪氨酸568磷酸化,导致Nrf2的核输出。在本研究中,我们调查了Fyn调控以及Fyn介导的Nrf2核输出的上游因子。这些研究揭示了Nrf2在氧化应激反应中的一种新调控机制。我们证明糖原合成酶激酶3β(GSK-3β)在控制Nrf2核输出方面作用于Fyn激酶的上游。化学抑制剂和短发夹RNA介导的对GSK-3β的抑制导致Nrf2在细胞核中积累以及Nrf2下游基因nqo1的转录激活。化学抑制剂和短发夹RNA分别及联合抑制GSK-3β和Fyn表明,这两种激酶遵循相同途径调控Nrf2的核输出。我们进一步证明过氧化氢使GSK-3β的酪氨酸216磷酸化。这导致GSK-3β激活。激活的GSK-3β使Fyn的苏氨酸残基磷酸化。磷酸化的Fyn在细胞核中积累并使Nrf2的酪氨酸568磷酸化。这导致Nrf2的核输出、泛素化和降解。