The human hypoxia-inducible factor 1α gene:: HIF1A structure and evolutionary conservation

被引:141
作者
Iyer, NV
Leung, SW
Semenza, GL
机构
[1] Johns Hopkins Univ, Sch Med, Inst Med Genet, Dept Pediat, Baltimore, MD 21287 USA
[2] Johns Hopkins Univ, Sch Med, Inst Med Genet, Dept Med, Baltimore, MD 21287 USA
关键词
D O I
10.1006/geno.1998.5416
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
The HIF1A gene encodes the HIF-1 alpha subunit of hypoxia-inducible factor 1, a transcription factor that is essential for cardiovascular development and systemic O-2 homeostasis. HIF1A consists of 15 exons that are interrupted by introns at the same locations as in the mouse Hif1a gene, although sequences mediating alternative splicing and alternative translation initiation events in the mouse are not present in the human gene. Placement of introns differs between HIF1A and EPAS1, which encodes the human HIF-2 alpha protein. Transcription of the HIF1A gene was initiated over a 15-nt region downstream of two SP1 sites. A 0.7-kb region of 5' flanking sequences functioned as a strong promoter in transient expression assays. Comparison of 0.8 kb of 5' flanking and 5' untranslated sequences from the HIF1A and Hif1a genes revealed 70% identity. The proximal 300 bp of 5' flanking sequences was 83% identical, including the SP1 sites and transcription initiation sites. These results suggest evolutionary selection for maintenance of HIF1A structure, function, and regulation. (C) 1998 Academic Press.
引用
收藏
页码:159 / 165
页数:7
相关论文
共 26 条
  • [1] BERGERON M, 1997, J CEREB BLOOD FLO S1, V17, pS505
  • [2] BREATHNACH R, 1981, ANNU REV BIOCHEM, V50, P349, DOI 10.1146/annurev.bi.50.070181.002025
  • [3] PURIFICATION AND BIOCHEMICAL-CHARACTERIZATION OF THE PROMOTER-SPECIFIC TRANSCRIPTION FACTOR, SPL
    BRIGGS, MR
    KADONAGA, JT
    BELL, SP
    TJIAN, R
    [J]. SCIENCE, 1986, 234 (4772) : 47 - 52
  • [4] 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
    Ema, M
    Taya, S
    Yokotani, N
    Sogawa, K
    Matsuda, Y
    FujiiKuriyama, Y
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1997, 94 (09) : 4273 - 4278
  • [5] 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
    Flamme, I
    Frohlich, T
    vonReutern, M
    Kappel, A
    Damert, A
    Risau, W
    [J]. MECHANISMS OF DEVELOPMENT, 1997, 63 (01) : 51 - 60
  • [6] Forsythe JA, 1996, MOL CELL BIOL, V16, P4604
  • [7] Characterization of a subset of the basic-helix-loop-helix-PAS superfamily that interacts with components of the dioxin signaling pathway
    Hogenesch, JB
    Chan, WK
    Jackiw, VH
    Brown, RC
    Gu, YZ
    PrayGrant, M
    Perdew, GH
    Bradfield, CA
    [J]. JOURNAL OF BIOLOGICAL CHEMISTRY, 1997, 272 (13) : 8581 - 8593
  • [8] Cellular and developmental control of O2 homeostasis by hypoxia-inducible factor 1α
    Iyer, NV
    Kotch, LE
    Agani, F
    Leung, SW
    Laughner, E
    Wenger, RH
    Gassmann, M
    Gearhart, JD
    Lawler, AM
    Yu, AY
    Semenza, GL
    [J]. GENES & DEVELOPMENT, 1998, 12 (02) : 149 - 162
  • [9] Dimerization, DNA binding, and transactivation properties of hypoxia-inducible factor 1
    Jiang, BH
    Rue, E
    Wang, GL
    Roe, R
    Semenza, GL
    [J]. JOURNAL OF BIOLOGICAL CHEMISTRY, 1996, 271 (30) : 17771 - 17778
  • [10] Transactivation and inhibitory domains of hypoxia-inducible factor 1 alpha. Modulation of transcriptional activity by oxygen tension
    Jiang, BH
    Zheng, JZ
    Leung, SW
    Roe, R
    Semenza, GL
    [J]. JOURNAL OF BIOLOGICAL CHEMISTRY, 1997, 272 (31) : 19253 - 19260