Skip to main content
. 2021 Jun 29;12:702930. doi: 10.3389/fpls.2021.702930

Table 2.

Genotypes of T3 Camelina progenies revealed by Sanger sequencing following homoeolog-specific PCR.

Line FAD2-1 FAD2-2 FAD2-3 Genotype
Zygosity Mutation Zygosity Mutation Zygosity Mutation
EC#5-1-1 hom. 1i+1i hom. 1i+1i WT WT aabbCC
EC#5-1-4 hom. 1i+1i hom. 1i+1i het. 1i aabbCc
EC#5-1-5 hom. 1i+1i bi. 1i+5d het. 1i aabbCc
EC#5-1-6 hom. 1i+1i hom. 1i+1i WT WT aabbCC
EC#5-1-22 hom. 1i+1i hom. 1i+1i het. 1i aabbCc
EC#5-1-24 hom. 1i+1i bi. 1i+5d het. 1i aabbCc
EC#5-6-14 bi. 1i+3d hom. 5d+5d het. 1i aa′bbCc
EC#5-6-18 bi. 1i+3d hom. 5d+5d hom. 1i+1i aa′bbcc
EC#5-6-23 hom. 1i+1i hom. 1i+1i hom. 1i+1i aabbcc
EC#5-6-24 bi. 1i+3d hom. 5d+5d het. 1i aa′bbCc
EC#5-7-9 bi. 1i+3d hom. 1i+1i het. 1i aa′bbCc
EC#5-7-19 hom. 1i+1i hom. 1i+1i hom. 1i+1i aabbcc
EC#5-7-20 hom. 3d+3d hom. 1i+1i hom. 1i+1i aabbcc
EC#5-7-21 bi. 1i+3d hom. 1i+1i hom. 1i+1i aa′bbcc
EC#5-12-5 hom. 3d+3d hom. 1i+1i hom. 1i+1i a′a′bbcc
EC#5-20-8 hom. 1i+1i bi. 1i+5d WT WT aabbCC
EC#5-26-3 bi. 1i+3d hom. 1i+1i WT WT aa′bbCC
EC#5-26-10 bi. 1i+3d hom. 1i+1i het. 1i aa′bbCc
EC#5-26-20 bi. 1i+3d hom. 1i+1i het. 1i aa′bbCc
EC#5-26-22 hom. 1i+1i hom. 1i+1i hom. 1i+1i aabbcc
EC#5-26-24 bi. 1i+3d hom. 1i+1i hom. 1i+1i aa′bbcc
EC#5-35-4 bi. 1i+3d hom. 5d+5d het. 1i aa′bbCc
EC#5-35-15 hom. 1i+1i hom. 5d+5d hom. 1i+1i aabbcc
EC#5-35-17 hom. 3d+3d hom. 5d+5d het. 1i a′a′bbCc
EC#5-35-24 bi. 1i+3d hom. 5d+5d hom. 1i+1i aa′bbcc
EC#5-44-3 hom. 3d+3d bi. 1i+5d het. 1i a′a′bbCc
EC#5-44-11 hom. 3d+3d bi. 1i+5d hom. 1i+1i a′a′bbcc
EC#5-44-15 hom. 3d+3d hom. 5d+5d hom. 1i+1i a′a′bbcc
EC#5-44-20 hom. 3d+3d hom. 1i+1i hom. 1i+1i a′a′bbcc
EC#5-44-24 hom. 3d+3d bi. 1i+5d het. 1i a′a′bbCc

1i, 3d, and 5d indicate 1 nt insertion, 3 nt deletion, and 5 nt deletion, respectively. Bi., het., and hom. represent biallelic, heteroallelic, and homoallelic mutants, respectively. Uppercase letters, lowercase letters, and lowercase letters with ′ in the Genotype column represent an intact CsFAD2 homoeolog, a nonsense CsFAD2 mutant gene, and a missense CsFAD2 mutant gene with a 3 nt deletion, respectively. A, B, and C in the Genotype column represent CsFAD2-1, CsFAD2-2, and CsFAD2-3, respectively.