Cloning of hypoxia-inducible factor 1 alpha cDNA from chick embryonic ventricular myocytes

Citation
T. Takahashi et al., Cloning of hypoxia-inducible factor 1 alpha cDNA from chick embryonic ventricular myocytes, BIOC BIOP R, 281(4), 2001, pp. 1057-1062
Citations number
31
Categorie Soggetti
Biochemistry & Biophysics
Journal title
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS
ISSN journal
0006291X → ACNP
Volume
281
Issue
4
Year of publication
2001
Pages
1057 - 1062
Database
ISI
SICI code
0006-291X(20010309)281:4<1057:COHF1A>2.0.ZU;2-G
Abstract
Hypoxia-inducible factor 1 (HIF-1) is composed of HIF-1 alpha and arylhydoc arbon nuclear receptor translocator (ARNT), which belong to the basic-helix -loop-helix-Per/ARNT/Sim bHLH-PAS) family of transcription factors. HLF pla ys key roles in oxygen homeostasis and embryonic cardiovascular development . In this study, we have cloned cDNAs encoding the chick HIF-1 alpha from c ultured embryonic ventricular myocytes (CEVM) and then examined its express ion in various embryonic tissues. The deduced amino acid sequence of the ch ick HIF-1 alpha cDNA showed 79% identity with that of the human HIF-1 alpha cDNA. In contrast, sequence homology between the chick HIF-1 alpha and end othelial PAS protein 1 (EPAS1), another member of the bHLH-PAS proteins, wa s only low (49%). HIF-1 alpha mRNA was expressed abundantly in CEVM., but s carcely in the liver, which was quite different from expression pattern of EPAS1 mRNA. These data suggest that HIF-1 alpha may be involved in embryoni c cardiovascular development. HIF-1 alpha and EPAS1 may play distinct roles during developmental stages. (C) 2001 Academic Press.