Fig. 6: Regulation of lipid utilization gene expression by Pp4c, Snf1, and CreA in Magnaporthe oryzae. | Communications Biology

Fig. 6: Regulation of lipid utilization gene expression by Pp4c, Snf1, and CreA in Magnaporthe oryzae.

From: A multilayered regulatory network mediated by protein phosphatase 4 controls carbon catabolite repression and de-repression in Magnaporthe oryzae

Fig. 6

Relative expression level of lipase genes (a) and genes involved in fatty acid activation and transport, and β-oxidation (b), ICL1, and MCL1 (c) of ΔcreA in glucose and olive oil media relative to the wild-type. Relative expression level of lipase genes (d) and genes involved in fatty acid activation and transport, and β-oxidation (e), ICL1, and MCL1 (f) of Δsnf1 in glucose and olive oil media relative to the wild-type. Relative expression level of lipase genes (g) and genes involved in fatty acid activation and transport, and β-oxidation (h), ICL1, and MCL1 (i) of Δpp4c in glucose and olive oil media relative to the wild-type. H3 and α-ACTIN were used as reference genes. Error bars represent SD. Asterisks “*” indicate significant differences from the wild-type (Tukey's HSD test, p < 0.05). n = 3 biologically independent samples. j Schematic diagram of lipid metabolism regulation by Smek1, Pp4c, Snf1, CreA, and Crf1 in M. oryzae. Data for Smek1 and Crf1 were obtained from previous studies10,11.

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