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. 2016 Apr 18;113(18):5101–5106. doi: 10.1073/pnas.1522466113

Fig. S1.

Fig. S1.

Phenotypic characterization of cfr1 mutants. (A) Area of pericycle or pericycle-derived callus layer in longitudinal direction of the WT, slr, and three cfr1 allele roots incubated on CIM for 4 d. n = 18. Error bars are SD. Significance was determined by one-way ANOVA with Tukey's test. *P < 0.05. (B) Primary root length and lateral root initiates of WT, slr, and three alleles of cfr1 incubated on the MS containing different concentrations of NAA. n = 18. Error bars are SD. (C) Gravitropism of WT, slr, and three alleles of cfr1 roots. Here 4-d-old seedlings subjected to gravitropic assay and reorientation of roots for 50 seedlings in each genotype after 24 h were assigned to 1 of 12 30° sectors. (Scale bar: 10%.) (D and E) Morphology (D) and plant height (E) of 50-d-old seedlings of WT, slr, and cfr1 alleles. n = 19. Error bars are SD. Significance was determined by Student’s t test. ***P < 0.001. (Scale bar: 5 cm.) (F) Rosette leaf numbers of the WT, slr, and cfr1 plants before bolting. n = 19. Error bars are SD. Significance was determined by Student’s t test. ***P < 0.001.