Short-Term Hypoxia in Cells Induces Expression of Genes Which Are Enhanced in Stressed Cells

All living organisms must respond to, and defend against, environmental stresses. Depending on the extent and severity of stress, cells try to alter their metabolism and adapt to a new state. Changes in alternative splicing of pre-mRNA are a crucial regulation mechanism through which cells are able to respond to a decrease in oxygen tension in the cellular environment. Currently, only limited data are available in the literature on how short-term hypoxia influences mRNA isoform formation. In this work, we discovered that expressions of the same genes that are activated during cellular stress are also activated in cells under short-term hypoxic conditions. Our results demonstrate that short-term hypoxia influences the splicing of genes associated with cell stress and apoptosis; however, the mRNA isoform formation patterns from the same pre-mRNAs in cells under short-term hypoxic conditions and prolonged hypoxia are different. Obtained data also show that short-term cellular hypoxia increases protein phosphatase but not protein kinase expression. Enhanced levels of protein phosphatase expression in cells are clearly important for changing mRNA isoform formation.

Automated summary

This article investigates the effects of short-term hypoxia on gene splicing and protein expression. The study found that the splicing of genes associated with cellular stress changes under short-term hypoxic conditions, but differs from that under prolonged hypoxia. Additionally, short-term cellular hypoxia increases protein phosphatase expression, which is important for altering gene splicing.