Abstract

Tissues of symbiotic Cnidarians are exposed to wide, rapid and daily variations of oxygen concentration. Indeed, during daytime, intracellular O2 concentration increases due to symbiont photosynthesis, while during night, respiration of both host cells and symbionts leads to intra-tissue hypoxia. The Hypoxia Inducible Factor 1 (HIF-1) is a heterodimeric transcription factor used for maintenance of oxygen homeostasis and adaptation to hypoxia. Here, we carried out a mechanistic study of the response to variations of O2 concentrations of the coral model Stylophora pistillata. In silico analysis showed that homologs of HIF-1 α (SpiHIF-1α) and HIF-1β (SpiHIF-1β) exist in coral. A specific SpiHIF-1 DNA binding on mammalian Hypoxia Response Element (HRE) sequences was shown in extracts from coral exposed to dark conditions. Then, we cloned the coral HIF-1α and β genes and determined their expression and transcriptional activity. Although HIF-1α has an incomplete Oxygen-dependent Degradation Domain (ODD) relative to its human homolog, its protein level is increased under hypoxia when tested in mammalian cells. Moreover, co-transfection of SpiHIF-1α and β in mammalian cells stimulated an artificial promoter containing HRE only in hypoxic conditions. This study shows the strong conservation of molecular mechanisms involved in adaptation to O2 concentration between Cnidarians and Mammals whose ancestors diverged about 1,200–1,500 million years ago.

Highlights

  • Corals (Anthozoa, Scleractinia) play a pivotal role in marine ecosystems and are at the basis of the foundation of coral reefs

  • The present study revealed that coral Hypoxia Inducible Factor (HIF) shares several structural and functional similarities with human HIFs

  • In the N-TAD, C-terminal Oxygendependent Degradation Domain (ODD) is present, but alignment of Stylophora pistillata and human HIFα showed a lack of the N-terminal ODD in SpiHIFα

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Summary

Introduction

Corals (Anthozoa, Scleractinia) play a pivotal role in marine ecosystems and are at the basis of the foundation of coral reefs. Whereas HIFβ is stable, HIFα is sensitive to oxygen concentration ([5] for review.) In mammals, the oxygen-dependent degradation domain (ODD) of HIF-1α is hydroxylated by prolyl hydroxylase domain (PHD) enzymes under normoxia. These proline residues are highly conserved in other mammalian forms of HIF-1α. Prolyl hydroxylation is blocked due to decreased levels of oxygen, which leads to the stabilization of HIF-1α and its entry into the nucleus via its nuclear translocator signal motif [8]. HIF-1α dimerizes with HIF-1β to form a functional HIF-1 that binds to the A/GCGTG consensus motif in target gene promoter regions, known as hypoxia-responsive elements (HREs). Corallian HIF-1 stimulates the transcription of an artificial promoter containing HRE sequences in mammalian cells, which strongly suggests a conserved function through evolution

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