Table 1. Phenotypic analysis of the F1 generation of acn2 and cts-1 crosses.
Genotype | MS* (%) | MS+Suc† (%) | FAcR‡ (%) |
---|---|---|---|
Col-0 (n=3) | 99±1 | NA | 0 |
Ler (n=3) | 100 | NA | 0 |
cts-1 (n=3) | 11±4 | 53±2 | >99 |
acn2 (n=3) | <1 | 35±4 | >99 |
cts-1×acn2 (n=6) | 5±2 | 49±17 | >99 |
Ler×acn2 (n=3) | 100 | NA | 0 |
Ler×cts-1 (n=3) | 100 | NA | 0 |
Col-0×acn2 (n=3) | 96±2 | NA | 0 |
*Approx. 100 seeds were sown on to agar plates containing half-strength MS salts, pH 5.7. The plates were incubated in the dark for 4 days before being transferred to the growth cabinet.
†Seeds that had not germinated were tranferred on to agar plates containing half-strength MS salts and 20 mM sucrose.
‡Seeds were sown directly on to agar plates containing half-strength MS salts, pH 5.7, 20 mM sucrose and 0.5 mM FAc. Seeds from mutants and mutant crosses were nicked 24 h after transfer to the growth cabinet.