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Fig. 5. Hormonal responses of wild type and ral1. (A,C,E-H,M-P,Q,S,U) Wild
type. (B,D,I-L,R,T,V) ral1. (A-D) Seedlings 1 week (A,B) or 3 weeks
(C,D) after callus induction on 2 mg/l 2,4-D. (E,F,I,J,M,N) Calli at the stage
of transfer to the induction medium (E,I,M) and 3 weeks after (F,J,N) the
transfer. Medium contained either 2 mg/l 2,4-D (E,F,I,J) or 1 mg/l 2,4-D
(M,N). (G,H,K,L,O,P) Sections through the calli in F (G,H), in J (K,L), or in
N (O,P). (Q-V) DR5-GUS expression in the root of 1-week-old seedlings grown
for 24 hours on filter paper moistened with water (Q,R), with 0.1 (S,T) or 1
(U,V) µM NAA. (W,X) Frequency of shoot (W) or root (X) regeneration via
somatic organogenesis in callus tissues grown on hormone-free medium (black
diamond, wild type; black triangle, ral1) or on medium supplemented
with cytokinin (black square, wild type; cross, ral1). The results
represent the mean±s.e.m. of two separate experiments each performed on
a population of 80-100 calli per genotype and per treatment. Difference
between wild-type and ral1 populations as determined by
repeated-measures analysis of variance (single-factor ANOVA) was significant
(P<0.001) at all time points. (Y) Relative elongation over 24
hours of wild-type seminal (white boxes) and adventitious (grey boxes) roots
and ral1 (black boxes) roots in the presence of 0.05 µM 2,4-D or
0.1 µM NAA. The results represent the mean±s.e.m. of two separate
experiments each performed on a population of 20-35 seedlings per genotype and
per treatment. Asterisks indicate the significance of difference between
wild-type and ral1 populations as determined by repeated-measures
analysis of variance (single-factor ANOVA).
*0.01 P<0.05,
**0.001 P<0.01. b, shoot base; pe, proembryonic
structure; s, scutellum. Scale bars: (A-D,E,F,I,J,M,N) 2 mm (G,K) 100 µm
(H,L,O,P) 25 µm (Q-V) 50 µm.
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