Hypoxia response elements in the aldolase A, enolase 1, and lactate dehydrogenase A gene promoters contain essential binding sites for hypoxia-inducible factor 1

被引:1422
作者
Semenza, GL
Jiang, BH
Leung, SW
Passantino, R
Concordet, JP
Maire, P
Giallongo, A
机构
[1] JOHNS HOPKINS UNIV,SCH MED,DEPT PEDIAT,CTR MED GENET,BALTIMORE,MD 21287
[2] JOHNS HOPKINS UNIV,SCH MED,DEPT MED,BALTIMORE,MD 21287
[3] CNR,IST BIOL SVILUPPO,I-90123 PALERMO,ITALY
[4] INST COCHIN GENET MOL,F-75014 PARIS,FRANCE
关键词
D O I
10.1074/jbc.271.51.32529
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
Hypoxia-inducible factor 1 (HIF-1) is a basic helix-loop-helix transcription factor which is expressed when mammalian cells are subjected to hypoxia and which activates transcription of genes encoding erythropoietin, vascular endothelial growth factor, and other pro teins that are important for maintaining oxygen homeostasis. Previous studies have provided indirect evidence that HIF-1 also regulates transcription of genes encoding glycolytic enzymes, In this paper we characterize hypoxia response elements in the promoters of the ALDA, ENO1, and Ldha genes, We demonstrate that HIF-1 plays an essential role in activating transcription via these elements and show that although absolutely necessary, the presence of a HIF-1 binding site alone is not sufficient to mediate transcriptional responses to hypoxia, Analysis of hypoxia response elements in the ENO1 and Ldha gene promoters revealed that each contains two functionally-essential HIF-1 sites arranged as direct and inverted repeats, respectively. Our data establish that functional hypoxia-response elements consist of a pair of contiguous transcription factor binding sites at least one of which contains the core sequence 5'-RCGTG-3' and is recognized by HIF-1. These results provide further evidence that the coordinate transcriptional activation of genes encoding glycolytic enzymes which occurs in hypoxic cells is mediated by HIF-1.
引用
收藏
页码:32529 / 32537
页数:9
相关论文
共 48 条
[41]   Oxygen sensing and response to hypoxia by mammalian cells [J].
Wang, GL ;
Semenza, GL .
REDOX REPORT, 1996, 2 (02) :89-96
[42]  
WANG GL, 1993, BLOOD, V82, P3610
[43]  
WANG GL, 1993, J BIOL CHEM, V268, P21513
[44]   PURIFICATION AND CHARACTERIZATION OF HYPOXIA-INDUCIBLE FACTOR-1 [J].
WANG, GL ;
SEMENZA, GL .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1995, 270 (03) :1230-1237
[45]   HYPOXIA-INDUCIBLE FACTOR-1 IS A BASIC-HELIX-LOOP-HELIX-PAS HETERODIMER REGULATED BY CELLULAR O-2 TENSION [J].
WANG, GL ;
JIANG, BH ;
RUE, EA ;
SEMENZA, GL .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1995, 92 (12) :5510-5514
[46]  
WEBSTER KA, 1987, MOL CELL BIOCHEM, V77, P19
[47]   COORDINATE RECIPROCAL TRENDS IN GLYCOLYTIC AND MITOCHONDRIAL TRANSCRIPT ACCUMULATIONS DURING THE INVITRO DIFFERENTIATION OF HUMAN MYOBLASTS [J].
WEBSTER, KA ;
GUNNING, P ;
HARDEMAN, E ;
WALLACE, DC ;
KEDES, L .
JOURNAL OF CELLULAR PHYSIOLOGY, 1990, 142 (03) :566-573
[48]   COOPERATIVE BINDING OF ETS-1 AND CORE BINDING-FACTOR TO DNA [J].
WOTTON, D ;
GHYSDAEL, J ;
WANG, SW ;
SPECK, NA ;
OWEN, MJ .
MOLECULAR AND CELLULAR BIOLOGY, 1994, 14 (01) :840-850