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. 2008 Dec 19;60(2):591–602. doi: 10.1093/jxb/ern306

Table 2.

Quantification of Verticillium dahliae biomass in Arabidopsis gene-silencing mutants by real-time PCR comparison of V. dahliae internal transcribed spacer (ITS) transcript levels (as a measure for fungal biomass) relative to Arabidopsis RuBisCo transcript levels (for equilibration) at 19–29 d post-inoculation with V. dahliae strain JR2

Gene name Genotype Symptom displaya Biomass fold changeb Significancec
Col-0 1
AGO1 ago1-27 Reduced 0.007 P <0.1
AGO7 ago7-2 Enhanced 3.174 P <0.2
DCL2 dcl2-1 Similar 0.829 No
DCL4 dcl4-2 Enhanced 2.422 P <0.05
HEN1 hen1-6 Reduced 0.045 P <0.1
HST hst1-1 Reduced 0.039 P <0.05
NRPD1a/SDE4 nrpd1a-3 Enhanced 1.816 P <0.2
RDR2 rdr2-4 Enhanced 2.701 P <0.05
RDR6/SDE1/SGS2 sgs2-1 Enhanced 2.279 P <0.05
rdr6-15 Enhanced 3.286 P <0.05
SDE3 sde3-4 Similar 1.674 No
SGS1 sgs1-1 Enhanced 3.729 P <0.05
SGS3/SDE2 sgs3-1 Enhanced 2.938 P <0.05
a

Symptom display upon V. dahliae inoculation when compared with Col-0 (also see Fig. 3).

b

The relative average fungal biomass is indicated as relative fold-change when compared with fungal biomass in V. dahliae-inoculated Col-0 plants of which the average fungal biomass was set to one.

c

Statistically significant differences are given as P-values according to a Student's t test with a 95% to an 80% confidence interval (P <0.05–0.2).