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. 2004 Mar;16(3):709–722. doi: 10.1105/tpc.018994

Table 2.

Cotyledon Abnormalities in A Subunit Mutants

Parental Genotype Monocot Cot Fusion Tricot Asymmetric Other Abnorm. Total Abnorm. % Mutant (Observed)a n (Total)
Ws 0.4 0.4 472
rcn1 0.2 0.2 0.4 100 506
Col 0.4 0.4 498
pp2aa2-1 <0.2 100 481
pp2aa3-1 0.2 0.2 100 485
rcn1 pp2aa2-1/+ 0.7 3.7 0.5 1.5 6.3 25 (18) 410
rcn1 pp2aa3-1/+ 0.3 0.3 4.8 0.8 1.1 7.3 25 (23) 357
rcn1 pp2aa3-1 2.1 1.4 13.4 6.2 6.2 28.9 100 97
pin1-6/+ 4.0 4.5 4.3 0.3 13.1 25 398
rcn1 pin1-6/+ 12.9 5.0 0.5 2.1 1.6 22.0 25 381
pid-9/+ 0.3 8.8 0.3 9.3 25 387
rcn1 pid-9/+ 0.7 0.7 13.7 0.4 0.4 16 25 278

Self-progeny of plants with the genotypes indicated were assayed for symmetry defects. For double mutant combinations that produce sterile plants, cotyledon phenotypes were scored in segregating families. Seedlings were grown for 7 d in the light on sterile medium and then scored for cotyledon abnormalities using a dissecting microscope. Numbers shown represent percentages (except those shown in italics). Blank spaces indicate that no seedlings exhibited the abnormal cotyledon phenotype specified. In all cases, a blank space indicates a value <0.26%.

a

In segregating families, 25% of the progeny are expected to be homozygous mutants. Numbers shown in parentheses indicate the observed percentage of progeny exhibiting the homozygous mutant phenotype.