The PAS superfamily: Sensors of environmental and developmental signals

被引:809
作者
Gu, YZ [1 ]
Hogenesch, JB [1 ]
Bradfield, CA [1 ]
机构
[1] Univ Wisconsin, Sch Med, Mcardle Lab Canc Res, Madison, WI 53706 USA
关键词
PAS domains; LOV domains; dioxin; hypoxia; circadian rhythm; signaling;
D O I
10.1146/annurev.pharmtox.40.1.519
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Over the past decade, PAS domains have been identified in dozens of signal transduction molecules and various forms have been found in animals, plants, and prokaryotes. In this review, we summarize this rapidly expanding research area by providing a detailed description of three signal transduction pathways that utilize PAS protein heterodimers to drive their transcriptional output. It is hoped that these model pathways can provide a framework for use in understanding the biology of the less well-understood members of this emerging superfamily, as well as of those to be characterized in the days to come. We use this review to develop the idea that most eukaryotic PAS proteins can be classified by functional similarities, as well as by predicted phylogenetic relationships. We focus on the alpha-class proteins, which often act as sensors of environmental signals, and the beta-class proteins, which typically act as broad-spectrum partners that target these heterodimers to their genomic targets.
引用
收藏
页码:519 / 561
页数:45
相关论文
共 266 条
[41]   TEMPORALLY REGULATED NUCLEAR ENTRY OF THE DROSOPHILA PERIOD PROTEIN CONTRIBUTES TO THE CIRCADIAN CLOCK [J].
CURTIN, KD ;
HUANG, ZJ ;
ROSBASH, M .
NEURON, 1995, 14 (02) :365-372
[42]   REGULATION OF TYROSINE-HYDROXYLASE GENE-EXPRESSION IN THE RAT CAROTID-BODY BY HYPOXIA [J].
CZYZYKKRZESKA, MF ;
BAYLISS, DA ;
LAWSON, EE ;
MILLHORN, DE .
JOURNAL OF NEUROCHEMISTRY, 1992, 58 (04) :1538-1546
[43]   Closing the circadian loop:: CLOCK-induced transcription of its own inhibitors per and tim [J].
Darlington, TK ;
Wager-Smith, K ;
Ceriani, MF ;
Staknis, D ;
Gekakis, N ;
Steeves, TDL ;
Weitz, CJ ;
Takahashi, JS ;
Kay, SA .
SCIENCE, 1998, 280 (5369) :1599-1603
[44]   CASCADE REGULATION OF NIF GENE-EXPRESSION IN RHIZOBIUM-MELILOTI [J].
DAVID, M ;
DAVERAN, ML ;
BATUT, J ;
DEDIEU, A ;
DOMERGUE, O ;
GHAI, J ;
HERTIG, C ;
BOISTARD, P ;
KAHN, D .
CELL, 1988, 54 (05) :671-683
[45]   ASSOCIATION OF THE DIOXIN RECEPTOR WITH THE MR 90,000 HEAT-SHOCK PROTEIN - A STRUCTURAL KINSHIP WITH THE GLUCOCORTICOID RECEPTOR [J].
DENIS, M ;
CUTHILL, S ;
WIKSTROM, AC ;
POELLINGER, L ;
GUSTAFSSON, JA .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1988, 155 (02) :801-807
[46]  
DENISON MS, 1991, BANB REPORT, V35, P337
[47]  
DENOMME MA, 1985, MOL PHARMACOL, V27, P656
[48]   Identification of genes differentially regulated by interferon α, β, or γ using oligonucleotide arrays [J].
Der, SD ;
Zhou, AM ;
Williams, BRG ;
Silverman, RH .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1998, 95 (26) :15623-15628
[49]   IN-VITRO ANALYSIS OF AH RECEPTOR DOMAINS INVOLVED IN LIGAND-ACTIVATED DNA RECOGNITION [J].
DOLWICK, KM ;
SWANSON, HI ;
BRADFIELD, CA .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1993, 90 (18) :8566-8570
[50]   Cloning and selective expression in brain and kidney of ARNT2 homologous to the Ah receptor nuclear translocator (ARNT) [J].
Drutel, G ;
Kathmann, M ;
Heron, A ;
Schwartz, JC ;
Arrang, JM .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1996, 225 (02) :333-339