4.6 Article

Ubiquitin-specific Protease 19 (USP19) Regulates Hypoxia-inducible Factor 1α (HIF-1α) during Hypoxia

Journal

JOURNAL OF BIOLOGICAL CHEMISTRY
Volume 287, Issue 3, Pages 1962-1969

Publisher

ELSEVIER
DOI: 10.1074/jbc.M111.305615

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Funding

  1. Swedish Research council
  2. Karolinska Institutet
  3. Magn Bergvalls stiftelse
  4. Ake Wibergs Stiftelse
  5. Swedish Cancer Society
  6. ERACOL

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A proper cellular adaptation to low oxygen levels is essential for processes such as development, growth, metabolism, and angiogenesis. The response to decrease in oxygen supply, referred to as hypoxia, is also involved in numerous human diseases including cancer, inflammatory conditions, and vascular disease. The hypoxia-inducible factor 1-alpha (HIF-1 alpha), a key player in the hypoxic response, is kept under stringent regulation. At normoxia, the levels are kept low as a consequence of the efficient degradation by the ubiquitin-proteasome system, and in response to hypoxia, the degradation is blocked and the accumulating HIF-1 alpha promotes a transcriptional response essential for proper adaptation and survival. Here we show that the ubiquitin-specific protease-19 (USP19) interacts with components of the hypoxia pathway including HIF-1 alpha and rescues it from degradation independent of its catalytic activity. In the absence of USP19, cells fail to mount an appropriate response to hypoxia, indicating an important role for this enzyme in normal or pathological conditions.

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