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. 2020 Apr 20;71(16):4972–4984. doi: 10.1093/jxb/eraa193

Fig. 3.

Fig. 3.

CLE transcript abundances measured by RT–qPCR. (A) Transcript abundance of M. truncatula CLE genes from the identified clade, except for MtCLE12 and MtCLE13, in roots of plants grown at low P (6 μM Pi), high P (600 μM Pi), and low P inoculated with arbuscular mycorrhizal fungi (AMF) (6 μM Pi). For each transcript, low P expression levels were normalized to 1. Bars are average values ±SD (n=5). Different letters indicate significant differences between individual CLE transcript abundances based on one-way ANOVA followed by Tukey´s post-hoc test (P<0.05). (B) Transcriptional response of MtCLE53 to AMF colonization in the wild type and mtpt4. (C) Transcriptional responses in the wild type and mtpt4 of MtCLE53 in the AMF-colonized root half (AMF) compared with the non-colonized root half (NM) in a split-root system. Bars are averages ± SD (n=3). Significant differences in (B) and (C) are marked with asterisks (*) and were calculated based on two-sided Student’s t-test (P<0.05).