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Results and Discussions
Analysis of the meiotic chromosome configurations of F1 plants
shows that mean value of rod bivalents per cell was 0.8 in Norrona and
0.6 in T-13, while in monosomic hybrids CS x T-13 it was higher and equals
to about 3 bivalents per cell (Tables 1 and
2). The chromosome pairing in hybrids F1
was less regular than in their parent plants and associations between
chromosomes during meiosis were rather weak, which resulted in premature
disjoining of bivalents and increase in number of additional univalents.
Taking into account percent of PMC with the normal chromosome configurations
at MI in F1 monosomic hybrids (20II+1I)
it was found that some chromosomes of variety Norrona and mutant T-13
affected pairing in meiosis. Thus, in monosomic F1 plants from
crosses CS x Norrona chromosomes 4A and 4B decreased pairing, whereas
chromosomes 1B and 3D increased it (Table 1).
In monosomic F1 plants from crosses CS x T-13 chromosome 3B
significantly decreased pairing, and in monosomic hybrids for chromosomes
5A, 1B and 7B meiosis was more regular as compared with F1
disomics (Table 2).
The existence of further structural differences between the chromosomes
of CS, on one hand, and variety Norrona and mutant T-13, on the other
hand, is supported by the data on chromosome configurations and multivalent
formations at MI in F1 plants from crosses of CS monosomics
with Norrona and mutant T-13.
The presence of reciprocal translocations between the chromosomes of wheat
varieties leads to irregular pairing and hybrids produce quadrivalents
and other chromosome associations at MI. With the monosomic hybrids, in
which one of the chromosome implicated in the translocation is absent,
trivalent configurations appears at meiosis (LAW & Worland 1972). The
critical F1 plants have a trivalents in a number of PMC, while
the non-critical plants have a quadrivalent configurations (Morris Sears
1967; LINDE-LAURSEN & LARSEN 1974). The occurrence of at least two trivalents
without univalents at MI in the F1 hybrids is indicative of
heterozygosity for chromosomal interchange.
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