4.5 Article

Hypoxia and hypoxia mimetics differentially modulate histone post-translational modifications

Journal

EPIGENETICS
Volume 16, Issue 1, Pages 14-27

Publisher

TAYLOR & FRANCIS INC
DOI: 10.1080/15592294.2020.1786305

Keywords

Hypoxia; histone post-translational modifications; epigenetics; hypoxia mimetics; epigenetics; HIF; intact protein mass spectrometry; iron chelating drugs; 2-oxoglutarate/alpha-ketoglutarate oxygenases

Funding

  1. Cancer Research UK [C8717/A18245]
  2. EPSRC
  3. Wellcome Trust [106244/Z/14/Z, FC001748]
  4. Ministry of National Defense-Medical Affairs Bureau, Taiwan
  5. William R. Miller Junior Research Fellowship at St. Edmund Hall, Oxford
  6. European Union's Horizon 2020 research and innovation programme under the Marie Sklodowska-Curie grant [657292]
  7. Francis Crick Institute - Cancer Research UK [FC001748]
  8. UK Medical Research Council [FC001748]
  9. BBSRC [BB/L009846/1] Funding Source: UKRI
  10. Marie Curie Actions (MSCA) [657292] Funding Source: Marie Curie Actions (MSCA)

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Hypoxia affects histone modifications, but synthetic hypoxia mimetics may not accurately replicate these effects. Liquid chromatography-mass spectrometry is a simple and robust method for investigating potential drug effects on histone modifications. The findings suggest caution should be used in interpreting data from chemically-induced hypoxia.
Post-translational modifications (PTMs) to the tails of the core histone proteins are critically involved in epigenetic regulation. Hypoxia affects histone modifications by altering the activities of histone-modifying enzymes and the levels of hypoxia-inducible factor (HIF) isoforms. Synthetic hypoxia mimetics promote a similar response, but how accurately the hypoxia mimetics replicate the effects of limited oxygen availability on the levels of histone PTMs is uncertain. Here we report studies on the profiling of the global changes to PTMs on intact histones in response to hypoxia/ hypoxia-related stresses using liquid chromatography-mass spectrometry (LC-MS). We demonstrate that intact protein LC-MS profiling is a relatively simple and robust method for investigating potential effects of drugs on histone modifications. The results provide insights into the profiles of PTMs associated with hypoxia and inform on the extent to which hypoxia and hypoxia mimetics cause similar changes to histones. These findings imply chemically-induced hypoxia does not completely replicate the substantial effects of physiological hypoxia on histone PTMs, highlighting that caution should be used in interpreting data from their use.

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