Inherent DNA-binding specificities of the HIF-1α and HIF-2α transcription factors in chromatin
journal contributionposted on 2019-12-19, 18:07 authored by James A Smythies, Min Sun, Norma Masson, Rafik Salama, Peter D Simpson, Elizabeth Murray, Viviana Neumann, Matthew E Cockman, Hani Choudhry, Peter J Ratcliffe, David R Mole
Hypoxia-inducible factor (HIF) is the major transcriptional regulator of cellular responses to hypoxia. The two principal HIF-α isoforms, HIF-1α and HIF-2α, are progressively stabilized in response to hypoxia and form heterodimers with HIF-1β to activate a broad range of transcriptional responses. Here, we report on the pan-genomic distribution of isoform-specific HIF binding in response to hypoxia of varying severity and duration, and in response to genetic ablation of each HIF-α isoform. Our findings reveal that, despite an identical consensus recognition sequence in DNA, each HIF heterodimer loads progressively at a distinct repertoire of cell-type-specific sites across the genome, with little evidence of redistribution under any of the conditions examined. Marked biases towards promoter-proximal binding of HIF-1 and promoter-distant binding of HIF-2 were observed under all conditions and were consistent in multiple cell type. The findings imply that each HIF isoform has an inherent property that determines its binding distribution across the genome, which might be exploited to therapeutically target the specific transcriptional output of each isoform independently.
Crick (Grant ID: 10501, Grant title: Ratcliffe FC001501)
HIFDNA bindinghypoxiatranscriptionBasic Helix-Loop-Helix Transcription FactorsCell HypoxiaCell LineChromatinDNADNA-Binding ProteinsEpigenomicsGene Expression RegulationHumansHypoxia-Inducible Factor 1, alpha SubunitPromoter Regions, GeneticProtein IsoformsTranscription, GeneticRatcliffe FC001501Developmental Biology0601 Biochemistry and Cell Biology