Endothelial PAS domain protein 1 (EPAS1), a transcription factor selectively expressed in endothelial cells

被引:1076
作者
Tian, H
McKnight, SL
Russell, DW
机构
[1] UNIV TEXAS,SW MED CTR,DEPT BIOCHEM,DALLAS,TX 75235
[2] UNIV TEXAS,SW MED CTR,DEPT MOL GENET,DALLAS,TX 75235
关键词
PAS domain proteins; endothelial cell transcription; receptor tyrpsine kinase; Tie-2; hypoxia inducible factor; chromosome; 2p16-213;
D O I
10.1101/gad.11.1.72
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Here we describe the cloning and characterization of a PAS domain transcription factor termed endothelial PAS-1 (EPAS1). This protein shares 48% sequence identity with hypoxia inducible factor (HIE-1 alpha) and lesser similarity with other members of the basic helix-loop-helix/PAS domain family of transcription factors. Like HIE-1 alpha, EPAS1 binds to and activates transcription from a DNA element originally isolated from the erythropoietin gene and containing the sequence 5'-GCCCTACGTGCTGTCTCA-3'. Activation by both HIF-1 alpha and EPAS1 is stimulated by hypoxic conditions. EPAS1 forms a heterodimeric complex with the aryl hydrocarbon nuclear transporter prior to transcriptional activation of target genes. EPAS1 expression is limited to the endothelium of mouse embryos and, in agreement with its cell type-specific expression pattern, is capable of specifically activating the transcription of the endothelial tyrosine kinase gene Tie-2. These observations raise the possibility that EPAS1 may represent an important regulator of vascularization, perhaps involving the regulation of endothelial cell gene expression in response to hypoxia.
引用
收藏
页码:72 / 82
页数:11
相关论文
共 56 条
[1]   CONSTITUTIVE FUNCTION OF THE BASIC HELIX-LOOP-HELIX PAS FACTOR ARNT - REGULATION OF TARGET PROMOTERS VIA THE E-BOX MOTIF [J].
ANTONSSON, C ;
ARULAMPALAM, V ;
WHITELAW, ML ;
PETTERSSON, S ;
POELLINGER, L .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1995, 270 (23) :13968-13972
[2]   EXPRESSION AND REGULATION OF STEROID 5-ALPHA-REDUCTASE IN THE UROGENITAL TRACT OF THE FETAL-RAT [J].
BERMAN, DM ;
TIAN, H ;
RUSSELL, DW .
MOLECULAR ENDOCRINOLOGY, 1995, 9 (11) :1561-1570
[3]   Hypoxia-induced paracrine regulation of vascular endothelial growth factor receptor expression [J].
Brogi, E ;
Schatteman, G ;
Wu, T ;
Kim, EA ;
Varticovski, L ;
Keyt, B ;
Isner, JM .
JOURNAL OF CLINICAL INVESTIGATION, 1996, 97 (02) :469-476
[4]   CLONING OF THE AH-RECEPTOR CDNA REVEALS A DISTINCTIVE LIGAND-ACTIVATED TRANSCRIPTION FACTOR [J].
BURBACH, KM ;
POLAND, A ;
BRADFIELD, CA .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1992, 89 (17) :8185-8189
[5]  
CHEN HS, 1994, J BIOL CHEM, V269, P27554
[6]   A FAMILY OF UNUSUALLY SPLICED BIOLOGICALLY-ACTIVE TRANSCRIPTS ENCODED BY A DROSOPHILA CLOCK GENE [J].
CITRI, Y ;
COLOT, HV ;
JACQUIER, AC ;
QIANG, Y ;
HALL, JC ;
BALTIMORE, D ;
ROSBASH, M .
NATURE, 1987, 326 (6108) :42-47
[7]   THE DISTRIBUTION OF CPG ISLANDS IN MAMMALIAN CHROMOSOMES [J].
CRAIG, JM ;
BICKMORE, WA .
NATURE GENETICS, 1994, 7 (03) :376-382
[8]  
DUMONT DJ, 1992, ONCOGENE, V7, P1471
[9]   VASCULARIZATION OF THE MOUSE EMBRYO - A STUDY OF FLK-1, TEK, TIE, AND VASCULAR ENDOTHELIAL GROWTH-FACTOR EXPRESSION DURING DEVELOPMENT [J].
DUMONT, DJ ;
FONG, GH ;
PURI, MC ;
GRADWOHL, G ;
ALITALO, K ;
BREITMAN, ML .
DEVELOPMENTAL DYNAMICS, 1995, 203 (01) :80-92
[10]   DOMINANT-NEGATIVE AND TARGETED NULL MUTATIONS IN THE ENDOTHELIAL RECEPTOR TYROSINE KINASE, TEK, REVEAL A CRITICAL ROLE IN VASCULOGENESIS OF THE EMBRYO [J].
DUMONT, DJ ;
GRADWOHL, G ;
FONG, GH ;
PURI, MC ;
GERTSENSTEIN, M ;
AUERBACH, A ;
BREITMAN, ML .
GENES & DEVELOPMENT, 1994, 8 (16) :1897-1909