Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
2031739 | Trends in Biochemical Sciences | 2008 | 9 Pages |
The hypoxia-inducible factor-1 (HIF-1) is the master regulator of the cellular response to hypoxia and its expression levels are tightly controlled through synthesis and degradation. It is widely accepted that HIF-1α protein accumulation during hypoxia results from inhibition of its oxygen-dependent degradation by the von Hippel Lindau protein (pVHL) pathway. However, recent data describe new pVHL- or oxygen-independent mechanisms for HIF-1α degradation. Furthermore, the hypoxia-induced increase in HIF-1α levels is facilitated by the continued translation of HIF-1α during hypoxia despite the global inhibition of protein translation. Recent work has contributed to an increased understanding of the mechanisms that control the translation and degradation of HIF-1α under both normoxic and hypoxic conditions.