As seen in Table l, in the 1995-1996
growing season, crossability percentages of D-genome substitutions of
Langdon with rye varied from 1.25 to 54.6. When the crossability
percentages were compared, it was shown that the substitution lines
4D(4B), 5D(5A), 6D(6A) and 7D(7A) were significantly higher than the
control, while 2D(2A), 2D(2B), 3D(3B) and 5D(5B) were significantly
lower than the control. Furthermore, 4D(4B) and 7D(7A) had a higher
crossability than 5D(5A), while 2D(2B) and 3D(3B) had a lower
crossability than 5D(5B), which was supported by the further studies
in the following growing season, as seen in Table
2 .
In fact, using an open pollinate rye as male tester, Genc et al.
(1996) have found that most of the 14 substitutions of Langdon showed
differences according to Langon, of which 7D(7A) had the highest
crossability with rye and 2D(2B) had the lowest crossability. They
suggested that the variation in crossability involved in the
relnainder chromosomes, except IA, 8B, 5A and 5B, was probably caused
by the heterozygosity present in the open pollinate rye parent, a
Turkish landrace. However, in this paper, because of using an inbred
rye as male parent, the variation can not be attributed to the
heterozygosity of rye. The previous works have shown that except the
weak kr3 on chromosome 5D, no other crossability genes have
been located on D-genome chromosome of cv. Chinese Spririg, which
provided the substituted D-genome chromosomes for the disomic
substitution lines in durum wheat Langdon. Krolow (1970) Iocated
kr3 on chromosome 5D, but other authors, such as Riley and
Chapman (1967), reported that kr3 has no significant effects
on crossability with rey. We think that the higher crossability than
control in lines 4D(4B), 5D(5A), 6D(6A) and 7D(7A) indicates that
chromosomes 4B, 5A, 6A and 7A of Langdon suppress crossability with
rye. The lower crossability in lines 2D(2A), 2D(2B), 3D(3B) and
5D(5B) indicates that chromosomes 2A, 2B, 3B and 5B of Langdon carry
crossability genes. Of which, chromosomes 2B and 3B showed a stronger
effect on crossability than chromosome 5B, and chromosomes 4B and 7A
showed a stronger effect than chromosome 5A.
On the other hand, the crossability genes in hexaploid wheat,
kr1, kr2, kr3 and kr4 were respectively
located on chromosome 5B, 5A, 5D and IA (Riley and Chapman 1967,
Krolow 1970, Zheng et al. 1992), and among them, the effect of
kr1 on chromosome 5B is the greatest. Thus, it is more logical
to suggest that tetraploid wheat cv. Langdon has a different
kr system regulating crossability with rye in comparison with
that of hexaploid wheat.
Meanwhile , the results of present study with regard to specific
substitution line show some differences in comparison with those
reported by Gene et al. (1996), such as the lines 4D(4B), 5D(5A) were
reported to have low crossabiltiy with rye whereas we obtained high
crossability. The differences may be caused by the different
cultivars of rye in the crosses.
Acknowledgments
The authors are highly thankful to Science and Technology
Committee of Sichuan Province for their financial support. We
particularly thank L.R. Joppa for providing the D-genome
substitutions of Langdon, and Mr. Y. Liu and Ms. Y. Zhou for
emasculation work.
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