Beyond antioxidant genes in the ancient Nrf2 regulatory network

被引:60
作者
Lacher, Sarah E. [1 ]
Lee, Joslynn S. [1 ]
Wang, Xuting [2 ]
Campbell, Michelle R. [2 ]
Bell, Douglas A. [2 ]
Slattery, Matthew [1 ,3 ]
机构
[1] Univ Minnesota, Sch Med, Dept Biomed Sci, Duluth, MN 55812 USA
[2] NIEHS, Environm Genom Sect, Genome Integr & Struct Biol Lab, NIH, Res Triangle Pk, NC 27709 USA
[3] Univ Minnesota, Ctr Dev Biol, Minneapolis, MN 55455 USA
基金
美国国家卫生研究院;
关键词
Nrf2; Keap1; ARE; Drosophila; Human; Genomics; Transcriptional regulation; Enhancer; Free radicals; OXIDATIVE STRESS-ADAPTATION; TRANSCRIPTION FACTOR NRF2; TERT-BUTYLHYDROQUINONE; PYRUVATE-CARBOXYLASE; ENRICHMENT ANALYSIS; FEEDBACK LOOP; FACTOR SKN-1; EXPRESSION; ACTIVATION; PATHWAYS;
D O I
10.1016/j.freeradbiomed.2015.06.044
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Nrf2, a basic leucine zipper transcription factor encoded by the gene NFE2L2, is a master regulator of the transcriptional response to oxidative stress. Nrf2 is structurally and functionally conserved from insects to humans, and it heterodimerizes with the small MAF transcription factors to bind a consensus DNA sequence (the antioxidant response element, or ARE) and regulate gene expression. We have used genome-wide chromatin immunoprecipitation and gene expression data to identify direct Nrf2 target genes in Drosophila and humans. These data have allowed us to construct the deeply conserved ancient Nrf2 regulatory network target genes that are conserved from Drosophila to human. The ancient network consists of canonical antioxidant genes, as well as genes related to proteasomal pathways and metabolism and a number of less expected genes. We have also used enhancer reporter assays and electrophoretic mobility-shift assays to confirm Nrf2-mediated regulation of ARE activity at a number of these novel target genes. Interestingly, the ancient network also highlights a prominent negative feedback loop; this, combined with the finding that Nrf2-mediated regulatory output is tightly linked to the quality of the ARE it is targeting, suggests that precise regulation of nuclear Nrf2 concentration is necessary to achieve proper quantitative regulation of distinct gene sets. Together, these findings highlight the importance of balance in the Nrf2-ARE pathway and indicate that Nrf2-mediated regulation of xenobiotic metabolism, glucose metabolism, and proteostasis has been central to this pathway since its inception. (C) 2015 Published by Elsevier Inc.
引用
收藏
页码:452 / 465
页数:14
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