| 초록 |
The level and activity of critical regulatory proteins in cells are tightly controlled by several tiers of post-translational modifications. HIF-1 alpha; is maintained at low levels under normoxia conditions by the collaboration between PHD proteins and the VHL-containing E3 ubiquitin ligase complex. We recently identified a new physiologically relevant mechanism that regulates HIF-1 alpha; stability in the nucleus in response to cellular oxygen levels. This mechanism is based on the collaboration between the SET7/9 methyltransferase and the LSD1 demethylase. SET7/9 adds a methyl group to HIF-1 alpha;, which triggers degradation of the protein by the ubiquitin-proteasome system, whereas LSD1 removes the methyl group, leading to stabilization of HIF-1 alpha; under hypoxia conditions. In cells from knock-in mice with a mutation preventing HIF-1 alpha; methylation (Hif1 alpha; KA/KA ), HIF-1 alpha; levels were increased in both normoxic and hypoxic conditions. Hif1 alpha; KA/KA knock-in mice displayed increased hematological parameters, such as red blood cell count and hemoglobin concentration. They also displayed pathological phenotypes; retinal and tumor-associated angiogenesis as well as tumor growth were increased in Hif1 alpha; KA/KA knock-in mice. Certain human cancer cells exhibit mutations that cause defects in HIF-1 alpha; methylation. In summary, this newly identified methylation-based regulation of HIF-1 alpha; stability constitutes another layer of regulation that is independent of previously identified mechanisms. |
