Identification of polymorphisms in the promoter region of the human NRF2 gene

被引:120
作者
Yamamoto, T
Yoh, K
Kobayashi, A
Ishii, Y
Kure, S
Koyama, A
Sakamoto, T
Sekizawa, K
Motohashi, H
Yamamoto, M
机构
[1] Univ Tsukuba, Grad Sch Comprehens Human Sci, Tsukuba, Ibaraki 3058577, Japan
[2] Univ Tsukuba, Ctr Tsukuba Adv Res Alliance, Tsukuba, Ibaraki 3058577, Japan
[3] Univ Tsukuba, Japan Sci & Technol Corp, Exploratory Res Adv Technol, Environm Response Project, Tsukuba, Ibaraki 3058577, Japan
[4] Tohoku Univ, Sch Med, Dept Med Genet, Sendai, Miyagi 9808574, Japan
基金
日本学术振兴会;
关键词
human NRF2 gene; transcription; initiator site; promoter; polymorphism; SNP; Japanese; 5 '-RACE; RNase protection; systemic lupus erythematosus; chronic obstructive pulmonary diseases;
D O I
10.1016/j.bbrc.2004.06.112
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
Transcription factor Nrf2 regulates the basal and inducible expression of detoxifying and antioxidant genes, Recent studies using nrf2-null mice suggest that Nrf2 dysfunction might be involved in the pathogenesis of human diseases. To gain insight into the relationship between impairment in the NRF2 gene and human diseases, we attempted to identify polymorphisms in the human NRF2 gene. We deter-mined the structure of the NRF2 gene and found three single nucleotide polymorphisms and one triplet repeat polymorphism in its regulatory region. These results provide a molecular basis for the genetic analysis of the NRF2 gene. The frequency of each polymorphism was examined in two groups of patients with systemic lupus erythematosus and chronic obstructive pulmonary disease. This study did not reveal a close connection between the risk of these diseases and the polymorphisms. However, available lines of evidence suggest the importance of examining the link between NRF2 polymorphisms and other oxidative stress-related diseases. (C) 2004 Elsevier Inc. All rights reserved.
引用
收藏
页码:72 / 79
页数:8
相关论文
共 29 条
[1]   Accelerated DNA adduct formation in the lung of the Nrf2 knockout mouse exposed to diesel exhaust [J].
Aoki, Y ;
Sato, H ;
Nishimura, N ;
Takahashi, S ;
Itoh, K ;
Yamamoto, M .
TOXICOLOGY AND APPLIED PHARMACOLOGY, 2001, 173 (03) :154-160
[2]  
CHAN JY, 1995, HUM GENET, V95, P265
[3]   Nrf2 is essential for protection against acute pulmonary injury in mice [J].
Chan, KM ;
Kan, YW .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1999, 96 (22) :12731-12736
[4]   Role of NRF2 in protection against hyperoxic lung injury in mice [J].
Cho, HY ;
Jedlicka, AE ;
Reddy, SP ;
Kensler, TW ;
Yamamoto, M ;
Zhang, LY ;
Kleeberger, SR .
AMERICAN JOURNAL OF RESPIRATORY CELL AND MOLECULAR BIOLOGY, 2002, 26 (02) :175-182
[5]   Linkage analysis of susceptibility to hyperoxia -: Nrf2 is a candidate gene [J].
Cho, HY ;
Jedlicka, AE ;
Reddy, SPM ;
Zhang, LY ;
Kensler, TW ;
Kleeberger, SR .
AMERICAN JOURNAL OF RESPIRATORY CELL AND MOLECULAR BIOLOGY, 2002, 26 (01) :42-51
[6]   High sensitivity of Nrf2 knockout mice to acetaminophen hepatotoxicity associated with decreased expression of ARE-regulated drug metabolizing enzymes and antioxidant genes [J].
Enomoto, A ;
Itoh, K ;
Nagayoshi, E ;
Haruta, J ;
Kimura, T ;
O'Connor, T ;
Harada, T ;
Yamamoto, M .
TOXICOLOGICAL SCIENCES, 2001, 59 (01) :169-177
[7]   Sulforaphane inhibits extracellular, intracellular, and antibiotic-resistant strains of Helicobacter pylori and prevents benzo[a]pyrene-induced stomach tumors [J].
Fahey, JW ;
Haristoy, X ;
Dolan, PM ;
Kensler, TW ;
Scholtus, I ;
Stephenson, KK ;
Talalay, P ;
Lozniewski, A .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2002, 99 (11) :7610-7615
[8]  
Ferrigno O, 2001, NAT GENET, V28, P77, DOI 10.1038/88306
[9]   Genome screening in human systemic lupus erythematosus: Results from a second Minnesota cohort and combined analyses of 187 sib-pair families [J].
Gaffney, PM ;
Ortmann, WA ;
Selby, SA ;
Shark, KB ;
Ockenden, TC ;
Rohlf, KE ;
Walgrave, NL ;
Boyum, WP ;
Malmgren, ML ;
Miller, ME ;
Kearns, GM ;
Messner, RP ;
King, RA ;
Rich, SS ;
Behrens, TW .
AMERICAN JOURNAL OF HUMAN GENETICS, 2000, 66 (02) :547-556
[10]   Activation of the mouse heme oxygenase-1 gene by 15-deoxy-Δ12,14-prostaglandin J2 is mediated by the stress response elements and transcription factor Nrf2 [J].
Gong, PF ;
Stewart, D ;
Hu, B ;
Ning, L ;
Cook, J ;
Nel, A ;
Alam, J .
ANTIOXIDANTS & REDOX SIGNALING, 2002, 4 (02) :249-257