Isolation and characterization of the hypoxia-inducible factor 1β in Drosophila melanogaster

被引:21
作者
Ma, E
Haddad, GG
机构
[1] Yale Univ, Sch Med, Dept Pediat, Sect Resp Med, New Haven, CT 06520 USA
[2] Yale Univ, Sch Med, Dept Cellular & Mol Physiol, New Haven, CT 06520 USA
来源
MOLECULAR BRAIN RESEARCH | 1999年 / 73卷 / 1-2期
关键词
Drosophila; HIF-1; alpha; beta; anoxia;
D O I
10.1016/S0169-328X(99)00224-7
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
The hypoxia-inducible factor 1 (HIF-1), a heterodimer composed of alpha and beta subunits, plays an important role in the cellular response to O-2 deprivation. In this paper, Drosophila HIF-1 beta (dHIF-1 beta) homolog is cloned and characterized. Further, Northern analyses showed that dHIF-1 alpha and dHIF-1 beta expressed their highest level at an embryonic stage. From the pupal stage on, their expression was sharply reduced and maintained at a steady level. Anoxia treatment up-regulated the expression of the both alpha and beta subunits. Over-expression of dHIF-1 alpha in transgenic embryos resulted in embryonic lethality, while over-expression of dHIF-1 beta significantly prolonged fly recovery time from a 5-min anoxic stupor. The cloning and characterization dHIF-1 beta reported in this paper provide a framework for further genetic dissection of the HIF-1 complex in its role in the cellular or tissue response to O-2 deprivation. (C) 1999 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:11 / 16
页数:6
相关论文
共 36 条
[1]   Regulation of the Drosophila bHLH-PAS protein Sima by hypoxia:: Functional evidence for homology with mammalian HIF-1α [J].
Bacon, NCM ;
Wappner, P ;
O'Rourke, JF ;
Bartlett, SM ;
Shilo, B ;
Pugh, CW ;
Ratcliffe, PJ .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1998, 249 (03) :811-816
[2]   Role of HIF-1α or in hypoxia-mediated apoptosis, cell proliferation and tumour angiogenesis [J].
Carmeliet, P ;
Dor, Y ;
Herbert, JM ;
Fukumura, D ;
Brusselmans, K ;
Dewerchin, M ;
Neeman, M ;
Bono, F ;
Abramovitch, R ;
Maxwell, P ;
Koch, CJ ;
Ratcliffe, P ;
Moons, L ;
Jain, RK ;
Collen, D ;
Keshet, E .
NATURE, 1998, 394 (6692) :485-490
[3]  
CHOMCZYNSKI P, 1987, ANAL BIOCHEM, V162, P156, DOI 10.1016/0003-2697(87)90021-2
[4]   Control of cell lineage-specific development and transcription by bHLH-PAS proteins [J].
Crews, ST .
GENES & DEVELOPMENT, 1998, 12 (05) :607-620
[5]   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
[6]   A novel bHLH-PAS factor with close sequence similarity to hypoxia-inducible factor 1 alpha regulates the VEGF expression and is potentially involved in lung and vascular development [J].
Ema, M ;
Taya, S ;
Yokotani, N ;
Sogawa, K ;
Matsuda, Y ;
FujiiKuriyama, Y .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1997, 94 (09) :4273-4278
[7]   HYPOXIC REGULATION OF LACTATE-DEHYDROGENASE-A - INTERACTION BETWEEN HYPOXIA-INDUCIBLE FACTOR-1 AND CAMP RESPONSE ELEMENTS [J].
FIRTH, JD ;
EBERT, BL ;
RATCLIFFE, PJ .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1995, 270 (36) :21021-21027
[8]   HRF, a putative basic helix-loop-helix-PAS-domain transcription factor is closely related to hypoxia-inducible factor-1 alpha and developmentally expressed in blood vessels [J].
Flamme, I ;
Frohlich, T ;
vonReutern, M ;
Kappel, A ;
Damert, A ;
Risau, W .
MECHANISMS OF DEVELOPMENT, 1997, 63 (01) :51-60
[9]   O-2 DEPRIVATION IN THE CENTRAL-NERVOUS-SYSTEM - ON MECHANISMS OF NEURONAL RESPONSE, DIFFERENTIAL SENSITIVITY AND INJURY [J].
HADDAD, GG ;
JIANG, C .
PROGRESS IN NEUROBIOLOGY, 1993, 40 (03) :277-318
[10]   O-2-sensing mechanisms in excitable cells: Role of plasma membrane K+ channels [J].
Haddad, GG ;
Jiang, C .
ANNUAL REVIEW OF PHYSIOLOGY, 1997, 59 :23-42