Loss of nuclear factor E2-related factor 1 in the brain leads to dysregulation of proteasome gene expression and neurodegeneration

被引:133
作者
Lee, Candy S. [1 ]
Lee, Chiashan [1 ]
Hu, Terry [1 ]
Nguyen, Janice M. [1 ]
Zhang, Jiasheng [3 ]
Martin, Maureen V. [2 ]
Vawter, Marquis P. [2 ]
Huang, Eric J. [3 ]
Chan, Jefferson Y. [1 ]
机构
[1] Univ Calif Irvine, Dept Lab Med & Pathol, Irvine, CA 92697 USA
[2] Univ Calif Irvine, Dept Psychiat, Irvine, CA 92697 USA
[3] Univ Calif San Francisco, Dept Pathol, San Francisco, CA 94143 USA
基金
美国国家卫生研究院;
关键词
oxidative stress; conditional knockout; antioxidant response element; ANTIOXIDANT RESPONSE ELEMENT; TRANSCRIPTION FACTOR; UBIQUITIN SYSTEM; CORTICAL-NEURONS; NRF1; INHIBITION; CELLS; RECEPTOR; PATHWAY; DISEASE;
D O I
10.1073/pnas.1019209108
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
The ubiquitin-proteasome pathway plays an important role in the pathogenesis of neurodegeneration, but mechanisms controlling expression of components in this pathway remain poorly understood. Nuclear factor E2-related factor 1 (Nrf1) transcription factor has been shown to regulate expression of antioxidant and cytoprotective genes. To determine the function of Nrf1 in the brain, mice with a late-stage deletion of Nrf1 in neuronal cells were generated. Loss of Nrf1 leads to impaired proteasome function and neurodegeneration. Gene expression profiling and RT-PCR analysis revealed a coordinate down-regulation of various proteasomal genes including PsmB6, which encodes a catalytic subunit of the proteasome. Transcriptional analysis and chromatin immunoprecipitation experiments demonstrated that PsmB6 is an Nrf1 target gene. These findings reveal Nrf1 as a key transcriptional regulator required for the expression of proteasomal genes in neurons and suggest that perturbations of Nrf1 function may contribute to the pathogenesis of neurodegenerative diseases.
引用
收藏
页码:8408 / 8413
页数:6
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