Abstract:Growing tip of allooctoploid Triticale ‘h739’ plants and its pollen plants at the glume differentiation stage were cultured on MS medium supplemented with 2 mg/l 2,4-D. The callus began to be formed after 20 days. The induction frequency was up to 98.3%. By transferring subcultured calli to regeneration medium plantlet regeneration frequency was 95.2%. Five so- maclones HC-2, HC-3, HC-4, HC-5 and HC-0 have been selected; their plantlet regeneration frequency remained high through long-tern subculture, being more than 90% by 892 days. Most cells in HC-2 and HC-3 were haploidy (2n=28). Histological and scanning electron micros copy studies showed that callus of HC-3 was composed of embryoids at different developmental stages.