Dopamine receptor regulating factor, DRRF: A zinc finger transcription factor

被引:55
作者
Hwang, CK
D'Souza, UM
Eisch, AJ
Yajima, S
Lammers, CH
Yang, Y
Lee, SH
Kim, YM
Nestler, EJ
Mouradian, MM [1 ]
机构
[1] NINDS, Genet Pharmacol Unit, Expt Therapeut Branch, NIH, Bethesda, MD 20892 USA
[2] Univ Texas, SW Med Ctr, Dept Psychiat, Dallas, TX 75390 USA
关键词
D O I
10.1073/pnas.121635798
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
Dopamine receptor genes are under complex transcription control, determining their unique regional distribution in the brain. We describe here a zinc finger type transcription factor, designated dopamine receptor regulating factor (DRRF), which binds to Gc and GT boxes in the D-1A and D-2 dopamine receptor promoters and effectively displaces Spl and sp3 from these sequences. Consequently, DRRF can modulate the activity of these dopamine receptor promoters. Highest DRRF mRNA levels are found in brain with a specific regional distribution including olfactory bulb and tubercle, nucleus accumbens, striatum, hippocampus. amygdala, and frontal cortex. Many of these brain regions also express abundant levels of various dopamine receptors. In vivo, DRRF itself can be regulated by manipulations of dopaminergic transmission. Mice treated with drugs that increase extracellular striatal dopamine levels (cocaine), block dopamine receptors (haloperidol), or destroy dopamine terminals (1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine) show significant alterations in DRRF mRNA. The latter observations provide a basis for dopamine receptor regulation after these manipulations. We conclude that DRRF is important for modulating dopaminergic transmission in the brain.
引用
收藏
页码:7558 / 7563
页数:6
相关论文
共 48 条
[1]  
ANDERSON KP, 1995, MOL CELL BIOL, V15, P5957
[2]  
BRADLEY DJ, 1992, J NEUROSCI, V12, P2288
[3]   Dual function of the epithelial specific ets transcription factor, ELF3, in modulating differentiation [J].
Brembeck, FH ;
Opitz, OG ;
Libermann, TA ;
Rustgi, AK .
ONCOGENE, 2000, 19 (15) :1941-1949
[4]   CLONING OF AN INTRINSIC HUMAN TFIID SUBUNIT THAT INTERACTS WITH MULTIPLE TRANSCRIPTIONAL ACTIVATORS [J].
CHIANG, CM ;
ROEDER, RG .
SCIENCE, 1995, 267 (5197) :531-536
[5]   SYNERGISTIC ACTIVATION BY THE GLUTAMINE-RICH DOMAINS OF HUMAN TRANSCRIPTION FACTOR SP1 [J].
COUREY, AJ ;
HOLTZMAN, DA ;
JACKSON, SP ;
TJIAN, R .
CELL, 1989, 59 (05) :827-836
[6]  
Crossley M, 1996, MOL CELL BIOL, V16, P1695
[7]   Antipsychotic regulation of dopamine D1, D2 and D3 receptor mRNA [J].
D'Souza, U ;
McGuffin, P ;
Buckland, PR .
NEUROPHARMACOLOGY, 1997, 36 (11-12) :1689-1696
[8]   Characterization of the 5′ flanking region of the rat D3 dopamine receptor gene [J].
D'Souza, UM ;
Wang, W ;
Gao, DQ ;
Kanda, S ;
Lee, G ;
Junn, E ;
Hwang, CK ;
Jose, PA ;
Mouradian, MM .
JOURNAL OF NEUROCHEMISTRY, 2001, 76 (06) :1736-1744
[9]   Drug addiction as dopamine-dependent associative learning disorder [J].
Di Chiara, G .
EUROPEAN JOURNAL OF PHARMACOLOGY, 1999, 375 (1-3) :13-30
[10]   THE CRYSTAL-STRUCTURE OF A 2 ZINC-FINGER PEPTIDE REVEALS AN EXTENSION TO THE RULES FOR ZINC-FINGER DNA RECOGNITION [J].
FAIRALL, L ;
SCHWABE, JWR ;
CHAPMAN, L ;
FINCH, JT ;
RHODES, D .
NATURE, 1993, 366 (6454) :483-487