Hypoxia results in an HIF-1-dependent induction of brain-specific aldolase C in lung epithelial cells

1 The Pulmonary Center and 2 Department of Biochemistry, Boston University School of Medicine, Boston, Massachusetts Submitted 9 March 2006 ; accepted in final form 20 June 2006 Aldolase C (EC 4.1.2.13 [EC] ) is a brain-specific aldolase isoform and a putative target of the transcription factor hypoxia-inducible factor (HIF)-1. We identified aldolase C as a candidate hypoxia-regulated gene in mouse lung epithelial (MLE) cells using differential display. We show that the message accumulates in a robust fashion when MLE cells are exposed to 1% oxygen and is inversely related to oxygen content. Induction in hypoxia is dependent on protein synthesis. We localized a hypoxia-responsive element (HRE) in the aldolase C promoter using a series of deletion and heterologous expression studies. The HRE overlaps with a region of the proximal aldolase C promoter that is also related to its brain-specific expression. The HRE contains an Arnt (HIF-1 ) and an HIF-1 site. We show that induction in hypoxia is dependent on the HIF-1 site and that HIF-1 protein is present, by gel-shift assay, within nuclear complexes of MLE cells in hypoxia. Aldolase C mRNA expression is developmentally regulated in the fetal lung, rapidly downregulated in the newborn lung at birth, and inducible in the adult lung when exposed to hypoxia. This pattern of regulation is not seen in the brain. This preservation of this HRE in the promoters of four other species suggests that aldolase C may function as a stress-response gene. stress-response gene; zebrin II; perinatal; oxygen Address for reprint requests and other correspondence: M. Joyce-Brady, The Pulmonary Center, 715 Albany St., R304, Boston, MA 02118 (e-mail: mjbrady{at}bu.edu )