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Materials and methods

In addition to the dwarfing tetraploid wheat landrace Aiganfanmai, native to Shaaxi, China, the tall tetraploid wheat landrace Fenzhilanmai native to Sichuan, China and the hexaploid wheat variety, Tom Thumb were used as the cheek materials in the investigation of reaction to GA respectively. All the materials were obtained from Triticeae Research Institute, Sichuan Agricultural University, China. Aiganfanmai was crossed with Fenzhilanmai. Some F1 hybrids were selfed to obtain F2 seeds, the others-were crossed with Aiganfanmai to obtain BC1 seeds in the 1996-1997 cultivated season. The seeds of the two parents, the F1 and the F2 were sowed in the experiment field at the same day. Plants were kept 10 cm apart. All the seeds of each population were randomly planted with aids of label for identification. The backcross test was carried out in the 1997-1998 cultivated season by sowing the BC1 (F1 x Aiganfanmai) seeds in the field. Every internode length of the main stem was investigated at harvest. The length of all the internodes but the first one was recorded as the modified plant height.

The GA reaction test of seedlings was carried out on 45 unselected seeds from Aiganfanmai and Tom Thumb. Seeds were placed in petri dishes, moistened with running water for 1 day at 18-20C then grown for 2 days at 2C to ensure even germination. Half the germinated seeds were treated with 0.15 mM GA, and the other half were continuously grown in running water. After a further 6 days at 18-20oC with 12 hour light-12 hour dark period, the length of coleoptile and the first leaf were measured.


Results

Like other wheat plants, Aiganfanmai possessed seven internodes. Measurements indicate that all the internodes of Aiganfanmai were statistically shorter than those of the tall landrace, Fenzhilanmai except the first one (Table 1). The length of the first internode was mainly determined by the deepness of the seeds in soil. To some extent, the deeper the seeds were in soil, the longer the first internodes of stem were. This contributed to the non-correlation between the plant heights and the length of the first internode in 1996-1997 season (r=0.203, p=0.059). In addition, spike length of Aiganfanmai was 9.2 + or - 0.5 cm, which was obviously shorter than that of Fenzhilanmai (14.4 + or - 0.08 cm, p < 0.001). According to the previous report (Goud and Sridevi 1988), the spike length has its own genetic basis other than the Rht genes. So, the term plant height in this paper was designated to represent the total length of internodes from the second to the seventh, which was different from the term final plant height that included the length of both stem and spike in previous literature.

Aiganfamnai has been planted in our experiment field since 1993. The mean of plant height of Aiganfanmai varied considerably depending on the supply of water and artificial fertilizers in different cultivated seasons. However, the dwarf landrace Aiganfanmai was always very much shorter than the tall landrace Fenzhilanmai in the same season (Table 2). So, the dwarf trait of Aiganfanmai should have its genetic basis.

The mean plant height of the F1 progeny (Aiganfanmai x Fenzhilanmai) is much higher than that of Aiganfanmai, and more close to that of Fenzhilanmai (Fig. 1). This result indicates that the dwarf trait of Aiganfanmai is recessive. The F2 population segregated into dwarf and tall plants (Fig. 1). According to the plant height distributions we can arbitrate that the plants shorter than 106 cm are dwarf and those higher than 110 cm are tall in F2 Population. Thus, the F2 population comprised 85 dwarf plants (about 22.6 %) and 292 tall plants (about 77.4%). Chi2 analysis showed that the segregation of dwarf and tall plants in F2 population fitted to the ratio of 1 : 3 very well (chic2=1 .083, p=0.298). To confirm monohybrid segregation further, backcross test was carried out in 1997-1998 season. BC1 (F1 x Aiganfanmai) population segregated into 84 dwarfs (shorter than 100cm) and 74 talls (higher than 112cm). The segregation ratio fitted to the expected 1 : 1 very well (chic2=0.513, p=0.481). Thus, it is evident that the dwarf trait of Aiganfanmai is conditioned by one gene.

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