“…Tillers were collected from Fl hybrids and stored in the dark at 4°C for 3 weeks. Anthers were then collected at the mid-to late uninucleate microspore stage and transferred to petri dishes (35 X 10 mm) containing 5 ml of induction medium (14) supplemented with a trichothecene mixture (0.23 mg/liter DQN, 0.23 mg/liter 15-ADQN, 0.47 mg/liter NIV, and 0.7 mg/liter T-2 toxin; all from Sigma or Sigma-Aldrich, St. Louis, MO). After 6 weeks of incubation at 27 ± 1°C, scutellum stage embryos and embryo-like structures were transferred to regeneration medium, and plantlet regeneration, propagation, and DH production were conducted as described in Eudes et al (14), The parent genotype FEl, was previously produced using a similar method (F, Eudes, A. Comeau, S. Rioux, and J. Collin, unpublished data).…”