(go to KOMUGI Home) (go to WIS List) (go to NO.84 Contents)


Results

Production
The tetrageneric hybrid F1's were produced from crosses between trigeneric hybrids and doubled diploids or amphidiploids by means of in vitro culture of immature embryo. No high incompatibility was observed. The results of tetrageneric hybrids crossed between trigeneric hybrids (Triticale x Haynatriticum) and Agrotriticum, and their embryo cultures are shown in Table 1. Tetrageneric hybrid seeds were obtained easily, but most of the endosperms were poorly developed or absent. After the embryos had been rescued, ten and two tetrageneric hybrid plantlets were obtained from two cross combinations. Meanwhile, there was a significant difference in percentage of regenerated plantlets when Agrotriticums in different ploidy were used as the male parent.

Morphology
Seedlings of the tetrageneric hybrid F1's were transplanted to pots. Some hybrid plants were vigorous in vegetative appearance. The average number of spikes per plant was 11, varying from 4 to 23. All of the hybrid plants were immune to BYDV, powdery mildew and rusts. The leaves of the hybrid seedlings were wide and long, resembling those of common wheat. Their spikes varied widely in morphology, showing some phenotypes that could not be found in their parents. Some characters were peculiar to Haynaldia villosa, such as the midrib bristles on outer glume (Fig. 1), fragile internode of rachis. For characters such as resistance to BYDV, the hybrid plants were similar to their parents of Agrotriticum. The hairy neck appeared in the hybrid plants is a marked character to Secale cereale. The hybrid plants maintained these special characters inherited from the four genera, which were helpful to distinguish the true hybrids from the false.

Fertility
The hybrids were infertile or low-fertile types. The tetrageneric hybrids could produce seeds when selfed or backcrossed with wheat. Seed setting percentage averaged 1.2% when self-crossed. Some plants of hybrid F1 had no pollen or a few fertile pollens in the anther. Only 0.5% of the pollens could be stained by the solution of I2- KI in the cross combination of ((TS6xO x TH6xL) x TA6xA2) (Table 2). However, its seed setting rate was significantly improved when backcrossed with a parent of Triticum species such as durum wheat, which could reach at 36.6%.

Cytological examination on somatic cells
Observation on the somatic cells of tetrageneric hybrid F1's showed that most plants had 39 chromosomes in the cross combination of ((TS6xO x TH6xL) x TA6xA2) varied from 37 to 40. The chromosome numbers were 47 and 50 in two plants of ((TS6x1330 x TH6xH) x TA8x16-3) (Table 2). These materials and their derivatives are being analysed by using DNA markers of their chromosomes and GISH methods (Tomita et al. 1993, 1994; Ma et al. 1994).

Derivatives of the tetrageneric hybrids
All selfed and backcrossed seeds were placed on moist filter paper at room temperature. Most of the seeds did not germinate. The F2 plants segregated obviously in morphology. The seeds were similar to wheat in morphology. In F3 generation of ((TS6xO x TH6xL) x TA6xA2), 3 out of 15 seedlings were chlorines. This character was inherited from the parent of Agrotriticum. These seedlings died 40 days later after germination. Twenty-one derivatives of F3 generation have been obtained from the tetrageneric hybrids (Fig. 2). Some plants were morphologically similar to wheat and had good fertility. The seed set percentage was 32.7% on average, varying from 8.7% to 64.9%.


Discussion

Tetrageneric hybrids and their derivatives have been successfully obtained by means of immature embryo rescue when Agrotriticum, Haynatriticum and Triticale were used as bridge parents to overcome the incompatibility and the infertility of direct crossing between wild relative species of wheat. These materials are of particular interest to demonstrate the genomic rearrangement during wide crossing using molecular cytogenetic methods such as C-banding and in situ hybridization. They can also be used as initial materials to transfer multi-disease resistance into wheat through backcrossing and chromosome engineering.

This study demonstrated that the male parents with different ploidy can significantly affect the production of immature embryos and regenerating ability of seedlings through embryo culture. When all the parents used in ((TS6xO x TH6xL) x TA6xA2) were hexaploids, the production of immature embryos reached at 10%, obviously higher than that of 1.1% in ((TS6x1330 x TH6xH) x TA8x16-3). The regenerating ability of seedlings through embryo culture had similar result. Besides, reciprocal crosses, the parental combination and culture media also had some effects on regenerating ability of callus. For example, we found that hexaploid Triticale often causes incompatibility of crosses or sterility of hybrid seeds when used as a male parent.

The chromosomes of tetrageneric hybrids and their derivatives originated from R, V, E andwheat genomes. These materials with the same central genomes AA and BB can develop new types of multi-disease resistance when self-crossed and backcrossed, such as multi-genera's addition lines and multi-genera's translocation lines (Fernandez-Escobar and Martin, 1988). So far, many selfed derivatives have been obtained from the tetrageneric hybrids.

<--Back | -->Next

(go to KOMUGI Home) (go to WIS List) (go to NO.84 Contents)