Hypoxia-inducible factor induces cysteine dioxygenase and promotes cysteine homeostasis inCaenorhabditis elegans

Abstract

AbstractDedicated genetic pathways regulate cysteine homeostasis. For example, high levels of cysteine activate cysteine dioxygenase, a key enzyme in cysteine catabolism in most animal and many fungal species. The mechanism by which cysteine dioxygenase is regulated is largely unknown. In an unbiased genetic screen for mutations that activate cysteine dioxygenase (cdo-1) in the nematodeC. elegans,we isolated loss-of-function mutations inrhy-1andegl-9,which encode proteins that negatively regulate the stability or activity of the oxygen-sensing hypoxia inducible transcription factor (hif-1). EGL-9 and HIF-1 are core members of the conserved eukaryotic hypoxia response. However, we demonstrate that the mechanism of HIF-1-mediated induction ofcdo-1is largely independent of EGL-9 prolyl hydroxylase activity and the von Hippel-Lindau E3 ubiquitin ligase, the classical hypoxia signaling pathway components. We demonstrate thatC. elegans cdo-1is transcriptionally activated by high levels of cysteine andhif-1.hif-1-dependent activation ofcdo-1occurs downstream of an H2S-sensing pathway that includesrhy-1, cysl-1,andegl-9. cdo-1transcription is primarily activated in the hypodermis where it is also sufficient to drive sulfur amino acid metabolism. Thus, the regulation ofcdo-1byhif-1reveals a negative feedback loop that maintains cysteine homeostasis. High levels of cysteine stimulate the production of an H2S signal. H2S then acts through therhy-1/cysl-1/egl-9signaling pathway to increase HIF-1-mediated transcription ofcdo-1,promoting degradation of cysteine via CDO-1.