摘要
The transcription factor HIF-1 alpha (hypoxia inducible factor 1 alpha) has an essential role in the maintenance of oxygen homeostasis in metazoans. HIF-1 alpha expression and activity in the hypoxic response is regulated at the translation and post-translational levels. However, the mechanism and modulator of HIF-1 alpha translation during hypoxia is not fully understood. We found that HIF-1 alpha expression during hypoxia was upregulated by the microRNA 130 (miR-130) family. Levels of the miR-130 family are elevated under hypoxia, and their target is DDX6 mRNA, which is a component of the P-bodies. Furthermore, we found that a decrease of DDX6 expression by the miR-130 family enhanced the translation of HIF-1 alpha in an internal ribosome entry site element-dependent manner. These results reveal a new HIF-1 alpha translational mechanism and a role for P-bodies in hypoxic stress.
- 出版日期2011-8