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Wheat Information Service
Number 81:20-21 (1995)
Triticum aestivum -Triticum araraticum
hybrids and their cytology
J. 8. Bijral and T. It Sharma
SKUAST, Regional Agricultural Recearch Station, R S. Pura 181102
India
Triticum araraticum (wild form of Triticum timopheevi,
2n=4x=28,AAGG) has been considered a valuable source of resistance to
a number of wheat (Triticum aestivum, 2n=6x=42, AABBDD)
pathogens, particularly Puccinia graminis tritici, P.
recondite tritici, Erysiphe graminis tritici and
Tilletia species (McIntosh and Gyarfas 1971). However, poor
crossability of T. araraticum with cultivated wheat is the
main barrier which precludes the transfer of resistance gene(s) from
the former to the latter species. Consequently, there are relatively
few reports on the successful transfer of disease resistance from
T. araraticum to common wheat (Allard and Shands 1954; Watson and
Luig 1968; McIntosh and Gyarfas 1971).
In order to transfer useful genes from T. araraticum to common
wheat, three wheat cvs. Chinese Spring (ph1b mutant), C 306
and HB 208 were crossed as females with T. araraticum (Acc.
No. 4697) under field conditions. Embryo culture or hormone
application was not employed and the crossed seed were harvested at
maturity. For meiotic studies, the spikes of the hybrids were fixed
in aceto-alcohol (1:3 vlv) for 24 hours and then stored in 70%
alcohol. The anthers were squashed in 2% acetocarmine and examined
for metaphase-1 chromosome relationships.
The number of florets pollinated for the three crosses, viz., ph1b
mutant x T. araraticum, C 306 x T.
araraticum and HB 208 x T. araraticum (hereafter Hy-1,
Hy-2 and Hy-3, respectively) were 40, 85 and 88, respectively and the
per cent seed set 37.5, 84.8 and 31.6, respectively. Depending on the
crossing directions and wheat genotypes with or without kr1
gene, seed set ranging from 8.8 to 84.0% has also been reported
by Farshadfar et al. (1994).
Hybrid plants derived from the three interspecific crosses were
partially fertile and there were 8.0, 1.2 and 3.0 weds per spike in
Hy-1, Hy-2 and Hy-3, respectively. The pollination of over 85 florets
of Hy-3 with wheat cv. RSP 122 produced 8 BC1 seeds. The percentage
germination of F2/BC1 seeds of Hy-1, Hy-2 and Hy-3, and
that of Hy-3 x RSP 122 was 13.3, 6.6, 8.0 and 12.5, respectively.
While Hy-3 and its backcross with RSP 122 await cytological analysis,
the data of meiotic chromosome pairing' pertaining to Hy-1 and Hy-2
are presented in Table 1. The pentaploid
hybrids (2n=5x=35, ABDAG) originating from ph1b mutant x T.
araraticum cross combination (Hy-1) showed univalents and
bivalents without multivalent formation. While number' of univalents
and bivalents ranged from 17- 21 and 7 - 9, respectively, the mean
bivalent frequency was 7.9 per cell.
Hy-2, on the other hand, was characterized by the formation of 28.1
univalents, 8.3 bivalents and 0.03 trivalents per cell. Of the
bivalents, 44.0% were ring and 56.0% rod configurations. Trivalent
association was recorded in one cell (3.4%) only. Increased level of
chromosome pairing in Hy-1 as compared with Hy-2 could be due. to the
absence of Ph gene.
Acknowledgements
Our thanks are due to Dr. G. S. Sethi, HPKV, Palampur and Dr. H.
S. Dhaliwal, PAU-Ludhiana for kindly providing seeds of Chinese
Spring (ph1b mutant) and T. araraticum (Acc. No.4697),
respectively.
References
Allard RW and Shands RG (1954) Inheritance of resistance to stem rust
and powdery mildew in stable spring wheats derived from Triticum
timopheevi. Phytopathology 44: 226-274.
Parshadfar M, Molnar-Lang M and Sutka, J (1994) The crossability of
different wheat (Triticum aestivum L.) genotypes with
Triticum timopheevi Zhuk under two types of conditions. Cereal
Res Comm 22: 15-20.
McIntosh RA and Gyarfas J (1971) Triticum timopheevi as
a source of resistance to wheat rust. Z Pflanzenzuchtg 66:
240-248.
Watson IA and Luig NH (1958) Timvera-A Steinwedel x Triticum
timopheevi derivative. Agron J 50: 644.
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