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. 2006 Jul;141(3):1128–1137. doi: 10.1104/pp.106.081059

Table II.

Analysis of progeny from crosses of mutants with wild type for cosegregation of the mutant phenotypes

ac, Acetate requiring; LS, no growth at 80 μE m−2 s−1; HLS, no growth at 500 μE m−2 s−1; LR, light resistant; lrc, light regulation of chlorophyll biosynthesis gene expression.

Crosses Performed Phenotypes of Progeny Assayed on Plates Regulatory Phenotypes of Eight Clonesa
ΔpetA (mt+) × 4A− (mt) 152ac, LS/12ac+, LR 4lrc, ac, mt/4lrc+, ac+, mt+a
petD-PWYE (mt+) × 4A− (mt) 94ac, LS/6ac+, LR 4lrc, ac, mt/4lrc+, ac+, mt+a
mcd1-F16 (mt) × 4A+ (mt+) 23ac, LS/24ac+, LR 4lrc, ac, LS/4lrc+, ac+, LR
tca1-693 (mt) × 4A+ (mt+) 21ac, LS/27ac+, LR 4lrc, ac, LS/4lrc+, ac+, LR
P1-15 (mt+) × 4A− (mt) 24ac, HLS/23ac+, LR 4lrc, ac, HLS/4lrc+, ac+, LR
P2-26 (mt+) × 4A− (mt) 20ac, LS/27ac+, LR 4lrc, ac, LS/4lrc+, ac+, LR
a

To ensure the analysis of recombinants (by RNA-blot techniques) from these crosses, the lrc phenotype was assayed only in ac progeny that was mt and in ac+ progeny that was mt+.