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. 2012 Jan 30;158(4):1503–1513. doi: 10.1104/pp.111.192856

Table II. Analysis of the intactness of the GUS expression cassette in plants regenerated from triticale microspores.

The presence and intactness of the integrated DNA carrying the GUS expression cassette were analyzed by PCR on genomic DNA isolated from triticale plants regenerated from microspores treated with DNA or DNA/protein complexes in the presence or absence of the Tat2 CPP or from untreated (control) microspores. Primers and segments of the GUS expression cassette, which contain the primer annealing sites, are indicated (Fig. 1; Supplemental Fig. S2).

Plants Containing the Amplified Regions of the Transgene Source DNA
Treatment P1-RS p7-p8 P1-Act p9-p10 Act-GUS p11-p12 Act-GUS p13-p3 Act-GUS p5-p3 GUS-nos p4-p6 GUS-nos p4-p14 GUS-nos p4-p15 GUS-P2 p4-p16 GUS-P2 p4-p17
No treatment 0 0 0 0 0 0 0 0 0 0
(21 plants) 0% 0% 0% 0% 0% 0% 0% 0% 0% 0%
No DNA + Tat2 0 0 0 0 1 2 2 2 0 0
(26 plants) 0% 0% 0% 0% 3.9% 7.7% 7.7% 7.7% 0% 0%
pACT-1D/PstI + Tat2 0 0 12 14 14 14 14 14 14 14
(63 plants) 0% 0% 19.1% 22.2% 22.2% 22.2% 22.2% 22.2% 22.2% 22.2%
dsT-DNA + Tat2 5 7 9 10 13 13 13 11 6 4
(44 plants) 11.4% 15.9% 20.5% 22.7% 29.6% 29.6% 29.6% 25.0% 13.6% 9.1%
ssT-DNA + Tat2 1 1 1 1 2 2 2 2 1 1
(27 plants) 3.7% 3.7% 3.7% 3.7% 7.4% 7.4% 7.4% 7.4% 3.7% 3.7%
ssT-DNA-RecA + Tat2 2 2 3 3 4 4 4 4 2 2
(23 plants) 8.7% 8.7% 13.0% 13.0% 17.4% 17.4% 17.4% 17.4% 8.7% 8.7%
VirD2-ssT-DNA + Tat2 3 3 4 5 6 6 5 4 3 3
(23 plants) 13.0% 13.0% 17.4% 21.7% 26.1% 26.1% 21.7% 17.4% 13.0% 13.0%
VirD2-ssT-DNA-RecA + Tat2 5 5 5 5 5 5 5 5 5 4
(20 plants) 25.0% 25.0% 25.0% 25.0% 25.0% 25.0% 25.0% 25.0% 25.0% 20%
No DNA 0 0 0 0 0 0 0 0 0 0
(14 plants) 0% 0% 0% 0% 0% 0% 0% 0% 0% 0%
pACT-1D/PstI 0 0 0 0 1 1 1 1 0 0
(Nine plants) 0% 0% 0% 0% 11.1% 11.1% 11.1% 11.1% 0% 0%
dsT-DNA 0 0 0 0 0 0 0 0 0 0
(Three plants) 0% 0% 0% 0% 0% 0% 0% 0% 0% 0%
VirD2-ssT-DNA-RecA 0 0 0 0 0 0 0 0 0 0
(10 plants) 0% 0% 0% 0% 0% 0% 0% 0% 0% 0%