Hypoxia inducible factor-1 (HIF-1) is a transcription factor composed of two subunits, HIF-1α and ARNT, which is activated under hypoxia. HIF-1α mRNA is expressed constitutively in a wide variety of cell types, whereas in some others HIF1A gene expression is upregulated by hypoxia. In this report, we show that in endothelial cells (HMEC-1) the HIF-1α mRNA expression level is the same in both normoxia and hypoxia. Deletion analysis experiments of the HIF1A promoter showed that in hypoxia HIF1A gene expression is upregulated through a short sequence located next to the transcription initiation site. We also show that in hypoxia another sequence located upstream from the +1 initiation site plays an inhibitory role on HIF1A transcription in HMEC-1 but not in hepatoma cells and brings back this expression level to that observed in normoxia. Finally, we demonstrate that HIF1A gene transcription is dependent on Sp1 binding sites and that the 5'UTR sequence also contains other important cis-acting elements.
|Pages (de - à)||534-540|
|Nombre de pages||7|
|journal||Biochemical and Biophysical Research Communications|
|Numéro de publication||2|
|Etat de la publication||Publié - 2 août 1999|