4.7 Article

Extensive regulation of the non-coding transcriptome by hypoxia: role of HIF in releasing paused RNApol2

Journal

EMBO REPORTS
Volume 15, Issue 1, Pages 70-76

Publisher

WILEY-BLACKWELL
DOI: 10.1002/embr.201337642

Keywords

HIF; hypoxia; non-coding; RNApol2; transcription

Funding

  1. Wellcome Trust [088182/Z/09/Z, 078333/Z/05/Z, WT091857MA]
  2. Higher Education Funding Council for England, Cancer Research UK [A16016]
  3. Ludwig Institute for Cancer Research
  4. Interdisciplinary Center of Clinical Research at the University of Erlangen-Nuremberg [TP J31]
  5. King Abdulaziz University, Ministry of High Education for Saudi Arabia
  6. Wellcome Trust [088182/Z/09/Z, 078333/Z/05/Z] Funding Source: Wellcome Trust
  7. Cancer Research UK [11359, 16016] Funding Source: researchfish
  8. National Institute for Health Research [NF-SI-0611-10163] Funding Source: researchfish

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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.

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