Abstract
Hypoxia is central to both ischaemic and neoplastic diseases. However, the non-coding transcriptional response to hypoxia is largely uncharacterized. We undertook integrated genomic analyses of both non-coding and coding transcripts using massively parallel sequencing and interfaced this data with pan-genomic analyses of hypoxia-inducible factor (HIF) and RNApol2 binding in hypoxic cells. These analyses revealed that all classes of RNA are profoundly regulated by hypoxia and implicated HIF as a major direct regulator of both the non-coding and coding transcriptome, acting predominantly through release of pre-bound promoter-paused RNApol2. These findings indicate that the transcriptional response to hypoxia is substantially more extensive than previously considered.
MeSH Terms
Basic Helix-Loop-Helix Transcription Factors/physiology
Cell Hypoxia
Gene Expression Regulation
Humans
Hypoxia-Inducible Factor 1, alpha Subunit/physiology
MCF-7 Cells
Promoter Regions, Genetic
Protein Binding
RNA Polymerase II/metabolism
RNA, Messenger/genetics,metabolism
RNA, Untranslated/genetics,metabolism
Transcription, Genetic
Transcriptome
Chemicals
Basic Helix-Loop-Helix Transcription Factors
HIF1A protein, human
Hypoxia-Inducible Factor 1, alpha Subunit
RNA, Messenger
RNA, Untranslated
endothelial PAS domain-containing protein 1
RNA Polymerase II
Authors & Affiliations
9 authors, click to expand affiliations / ORCID
Choudhry Hani
The Wellcome Trust Centre for Human Genetics, University of Oxford, Oxford, UK.
Schödel Johannes
Oikonomopoulos Spyros
Camps Carme
Grampp Steffen
Harris Adrian L
Ratcliffe Peter J
Ragoussis Jiannis
Mole David R
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