The core promoter of human thioredoxin reductase 1

被引:75
作者
Rundlöf, AK [1 ]
Carlsten, M [1 ]
Arnér, ESJ [1 ]
机构
[1] Karolinska Inst, Dept Med Biochem & Biophys, Nobel Inst Biochem, SE-17177 Stockholm, Sweden
关键词
D O I
10.1074/jbc.M101452200
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
The selenoprotein thioredoxin reductase 1 (TrxR1) carries many vital antioxidant and redox regulatory functions, Its mRNA levels are known to be post-transcriptionally modulated via AUUUA motifs (AU-rich elements (AREs)), but the promoter yet remains unknown. Here we. have cloned and determined the sequence of a 0.8-kilobase pair human genomic. fragment containing the proximal promoter for TrxR1, which has transcriptional. activity in several different cell types. The core promoter (-115 to +167) had an increased GC content and lacked TATA or CCAAT boxes. It contained a POU motif binding the Oct-1 transcription factor and two sites binding Sp1 and Sp3, which were identified with electrophoretic mobility shift assays using crude nuclear extracts of A549 cells. The TrxR1 promoter fulfills the typical criteria of a housekeeping gene. To our knowledge this is the first housekeeping-type promoter characterized for a gene with post-transcriptional regulation via ARE motifs generally possessed by transiently expressed proto-oncogenes, nuclear transcription factors, or cytokines and influencing mRNA stability in response to diverse exogenous factors. Expression of TrxR1 as an ARE-regulated housekeeping gene agrees with a role for the enzyme to maintain a balance between intracellular signaling via reactive oxygen species and protection of cells from excessive oxidative damage.
引用
收藏
页码:30542 / 30551
页数:10
相关论文
共 62 条
[31]   Molecular cloning and characterization of a mitochondrial selenocysteine-containing thioredoxin reductase from rat liver [J].
Lee, SR ;
Kim, JR ;
Kwon, KS ;
Yoon, HW ;
Levine, RL ;
Ginsburg, A ;
Rhee, SG .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1999, 274 (08) :4722-4734
[32]   Novel selenoproteins identified in silico and in vivo by using a conserved RNA structural motif [J].
Lescure, A ;
Gautheret, D ;
Carbon, P ;
Krol, A .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1999, 274 (53) :38147-38154
[33]  
Lickteig K, 1996, MOL REPROD DEV, V44, P146, DOI 10.1002/(SICI)1098-2795(199606)44:2<146::AID-MRD2>3.0.CO
[34]  
2-N
[35]   Human mitochondrial thioredoxin reductase -: cDNA cloning, expression and genomic organization [J].
Miranda-Vizuete, A ;
Damdimopoulos, AE ;
Pedrajas, JR ;
Gustafsson, JÅ ;
Spyrou, G .
EUROPEAN JOURNAL OF BIOCHEMISTRY, 1999, 261 (02) :405-412
[36]   Redox regulation of cellular activation [J].
Nakamura, H ;
Nakamura, K ;
Yodoi, J .
ANNUAL REVIEW OF IMMUNOLOGY, 1997, 15 :351-369
[37]   Stress-activated protein kinases (JNK and p38/HOG) are essential for vascular endothelial growth factor mRNA stability [J].
Pagès, G ;
Berra, E ;
Milanini, J ;
Levy, AP ;
Pouysségur, J .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2000, 275 (34) :26484-26491
[38]   Oct-4:: Lessons of totipotency from embryonic stem cells [J].
Pesce, M ;
Anastassiadis, K ;
Schöler, HR .
CELLS TISSUES ORGANS, 1999, 165 (3-4) :144-152
[39]   MatInd and MatInspector: New fast and versatile tools for detection of consensus matches in nucleotide sequence data [J].
Quandt, K ;
Frech, K ;
Karas, H ;
Wingender, E ;
Werner, T .
NUCLEIC ACIDS RESEARCH, 1995, 23 (23) :4878-4884
[40]   EMBOSS: The European molecular biology open software suite [J].
Rice, P ;
Longden, I ;
Bleasby, A .
TRENDS IN GENETICS, 2000, 16 (06) :276-277