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. Author manuscript; available in PMC: 2010 Jul 22.
Published in final edited form as: Dev Cell. 2009 Aug;17(2):268–278. doi: 10.1016/j.devcel.2009.06.007

Table 1.

Effect of loss-of-function of meristem identity genes on phenotype of 35S:SPL3Δ phenotype

Genotype Number of Rosette Leaves Number of Cauline Leaves Number of Secondary Inflorescence
Wild type (Col) 12.9 ± 0.2 (30) 3.2 ± 0.1 (30) 3.2 ± 0.1 (30)
35S:SPL3Δ 5.6 ± 0.2 (30) 1.6 ± 0.1 (30) 1.6 ± 0.1 (30)
35S:SPL3Δ lfy-1 5.5 ± 0.2 (ll) 11.6 ± 0.9 (11) 13.4 ± 0.1 (11)
lfy-1 13.5 ± 0.4 (12) 10.9 ± 0.5 (16) 21.3 ± 0.6 (16)
Wild type (Col) 12.5 ± 0.3 (12) 2.7 ± 0.1 (12) 2.7 ± 0.1 (12)
35S:SPL3Δ 5.5 ± 0.2 (42) 1.5 ± 0.1 (42) 1.5 ± 0.1 (42)
35S:SPL3Δ ful-2 9.6 ± 0.4 (12) 3.5 ± 0.2 (12) 3.5 ± 0.2 (12)
ful-2 11.8 ± 0.3 (11) 3.7 ± 0.2 (11) 3.7 ± 0.2 (11)
Wild type (Col) 12.6 ± 0.5 (7) 3.4 ± 0.3 (7) 3.4 ± 0.3 (7)
35S:SPL3Δ 5.7 ± 0.2 (30) 1.4 ± 0.1 (30) 1.4 ± 0.1 (30)
35S:SPL3Δ ap1-10 5.4 ± 0.2 (19) 1.8 ± 0.3 (19) 8.4 ± 1.6 (9)* 42.1%&
ap1-10 10.9 ± 0.5 (12) 3.2 ± 0.1 (12) 5.8 ± 1.0 (5)* 41.7%&

Shown is the mean ± SEM (n).

No statistically significant difference (Student's t test, P > 0.4) was detected between the marked genotypes.

Statistically significant difference (Student's t test, P < 0.05) was detected between marked genotypes.

*

Number of secondary inflorescences in plants that ceased secondary inflorescence and branched flower production prior to node 20.

&

% of plants that formed more than 20 secondary inflorescences and branched flowers. Plants were grown on soil at 22°C in long-day conditions (LDs; 16h light/8h dark, ~ 110 μmol/m2/s).