(A) Sampling scheme. Hv_Sym was cultured in the light-dark condition (Light: L) and in the continuous dark (Dark: D). Gene expression levels were examined by qPCR at 1, 2, 4 days for each condition (red arrows). (B) Expression difference of the genes in Hv_A99 between the two conditions. DEATH-1 and DEATH-2: Death domain containing proteins (gene ID: 6508 and rc_2417), TIR: Toll/interleukin-1 receptor domain containing protein (gene ID: 5168), PRKRIR: protein-kinase interferon-inducible double stranded RNA dependent inhibitor, repressor of (p58 repressor) (gene ID: rc_9398), ephrinR: ephrin receptor (gene ID: 26108), CLEC: C-type mannose receptor (gene ID: 11411), PRRT1: proline-rich transmembrane protein 1 (gene ID: rc_24563). For each biological replicate (n = 3) 50 hydra polyps were used for total RNA extraction. The vertical axis shows log scale (log2) fold change of relative expression levels in the light condition over the dark condition. Error bars indicate standard deviation. Pvalue of t-test, *<0.05, **<0.01.
Figure 2—figure supplement 1—source data 1. Hydra genes under influence of Chlorella photosynthesis examined by qPCR.