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Materials and methods
Thirty families, consisting of one hundred thirty-six plants,
were derived from two independent crosses of Triticum aestivum
L. em Thell. cvs. Wichita (WI) and Newton (NWT) with T. araraticum
(Fig. 1). The used accession of T.
araraticum., TA 39 from Iraq, is maintained at the Wheat Genetics
Resource Center, Kansas State University, Manhattan, Kansas, USA.
From two to 13 plants were analyzed in each family. A modified
C-banding technique was used for karyotype analysis (Badaeva et al.
1994). Chromosomes of common wheat, T. aestivum, and T.
araraticum were classified according to genetic nomenclature
(Gill et al. 1991; Badaeva et al. 1991).
Results and discussion
Cytogenetic analysis of hybrid lines showed that the majority of
plants had a chromosome number of 2n=42 (Fig.
2a). Two plants were exceptional. Plant #4 of KS88-9-8 with 2n=43
had a 5G(5B) 6G(6B) double disomic substitution and 4G monosomic
addition. Plant #3 of KS88-14-3 with 2n=41 was monosomic for 1 G(1B)
and had a double disomic 5At(5A) 6G(6B) substitution.
Twenty-six plants from eight families shared the common chromosome
rec 7AS-7AtL. Two plants of KS88-16-2 had one 6B and one
6G chromosome. Telocentric 5BL chromosome in homozygous or
heterozygous state was discovered in 11 plants of six families.
Twenty-eight plants belonging to nine families had a terminal
deletion of 1 BL (Fig. 2b). The modified 1 B
chromosome was present in homozygous condition in all plants of
KS88-17-1 and KS88-17-6, and was found in homozygous or heterozygous
condition in a few plants of the other families. The number of
substitutions per karyotype ranged from 0 to 3, and nine different
substitution types were recovered (Table
1).
The first type was found only in the KS88-2-2 family, where six
plants were homozygous and one plant was heterozygous for rec
7AS-7AtL chromosome. This chromosome had telomeric and
subtelomeric bands in the short and a faint proximal band near the
centromere in the long arm which were typical of normal chromosome
7A. A large intercalary C-band in the distal half of the 7At long arm
indicates that the cross-over site was probably located in the
proximal part of the long arms of 7A and 7At. Two types of
single disomic substitutions were found. Single 2G(2B) disomic
substitutions were identified in five families. In four of these
families the rec 7A-7At chromosome was also present.
Single disomic 6G(6B) substitution was found in six families. In
KS88-16-2, one plant was heterozygous for the rec 7A-7At
chromosome.
There were two types of double disomic substitution. Double disomic
substitution 3At(3A) 6G(6B) was found in all plants of KS88-7-2
family. One plant of KS88-14-3 and one plant of KS88-17-6 had a I G(I
D) 6G(6B) double disomic substitution.
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