Molecular assessment of the effect of light and heterotrophy in the scleractinian coral Stylophora pistillata.
Oren LevySarit Karako-LampertHiba Waldman Ben-AsherDidier ZoccolaGilles PagèsChristine Ferrier-PagèsPublished in: Proceedings. Biological sciences (2017)
Corals acquire nutrients via the transfer of photosynthates by their endosymbionts (autotrophy), or via zooplankton predation by the animal (heterotrophy). During stress events, corals lose their endosymbionts, and undergo starvation, unless they increase their heterotrophic capacities. Molecular mechanisms by which heterotrophy sustains metabolism in stressed corals remain elusive. Here for the first time, to the best of our knowledge, we identified specific genes expressed in heterotrophically fed and unfed colonies of the scleractinian coral Stylophora pistillata, maintained under normal and light-stress conditions. Physiological parameters and gene expression profiling demonstrated that fed corals better resisted stress than unfed ones by exhibiting less oxidative damage and protein degradation. Processes affected in light-stressed unfed corals (HLU), were related to energy and metabolite supply, carbohydrate biosynthesis, ion and nutrient transport, oxidative stress, Ca(2+) homeostasis, metabolism and calcification (carbonic anhydrases, calcium-transporting ATPase, bone morphogenetic proteins). Two genes (cp2u1 and cp1a2), which belong to the cytochrome P450 superfamily, were also upregulated 249 and 10 times, respectively, in HLU corals. In contrast, few of these processes were affected in light-stressed fed corals (HLF) because feeding supplied antioxidants and energetic molecules, which help repair oxidative damage. Altogether, these results show that heterotrophy helps prevent the cascade of metabolic problems downstream of oxidative stress.
Keyphrases
- oxidative stress
- genome wide identification
- genome wide
- dna damage
- mental health
- healthcare
- stress induced
- chronic kidney disease
- magnetic resonance imaging
- diabetic rats
- heat stress
- heavy metals
- binding protein
- single molecule
- protein protein
- postmenopausal women
- heat shock protein
- bone regeneration
- clinical evaluation
- heat shock