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Band polymorphism. could be due to (excluding banding protocols) the differential staining of GC:AT rich regions, somatic crossing-over, deletion/amplification of DNA sequences and structural rearrangements (Sumner 1990). Polymorphism is revealed as presence/absence of a band, in staining intensity and band size. Initially, it was argued that because of multiple origin and extensive introgression there could be no 'standard' banding pattern for many of the wheat chromosomes (Zurabishvili et al. 1978), but it did not gain support from other studies (Endo and Gill 1984). It is now possible to identify all wheat chromosomes by C-banding (Gill et al. 1991), which, among other things, has been used to localize translocation breakpoints (e.g. Friebe and Gill 1994; Taketa and Kawahara 1996).

The cultivation of wheat landraces in the Ethiopian highlands dates back ca. 5000 years (Feldman 1976). Conceivably, such wheats represent one isolated group of the earliest cultivated forms after the formation of the amphiploid(s). Although they showed little variation for gross karyomorphology (based on arm ratio), meiotic studies have revealed the presence of reciprocal translocations. Moreover, a remarkably high sterility was observed in some intervarietal/ intraspecific hybrids (Belay et al. 1994; Belay and Merker 1997).

The main objectives of the present study were; (1) to investigate C-band polymorphism in seven tetraploid wheat landrace morphotypes (=genotypes) of Ethiopian origin and, (2) to identify translocation breakpoints in five of them that are known to carry one reciprocal translocation each, relative to the standard Italian durum wheat variety, Senatore Capplelli (Belay and Merker 1997). We also compared our previous karyomorphology studies in non-banded chromosomes (Belay et al. 1994) with the results from C-banded ones.


Materials and methods

Plant material
Seven tetraploid wheat morphotypes, namely K-1-1, B-3-33, B-3-11, CD-7, A-4-34, A-1-116 and DZ-04-118 (an improved landrace variety through mass selection) were used. Their collection history and some of their morphological characteristics are given in Belay et al. (1994). Except for A-4-34 and A-1-1 16, all differed by one translocation each from Senatore Cappelli (SC) (Belay and Merker 1997), which was also included here for comparison purposes. The AB genome chromosomes of SC are structurally similar to those of the hexaploid cytogenetic reference, Chinese Spring (Perera et al. 1983). Seeds of SC were kindly supplied by Prof. Carla Ceoloni, Viterbo, Italy.

Cytology
The C-banding procedure employed was that of Gill et al. (1991) with minor changes. Band@nomenclature followed that of the same authors. For each morphotype, a minimum: of five metaphase plates from, at least, four plants each were analyzed. The karyotypes were compared mainly with those of the AB- genome chromosomes of hexaploid wheat varieties reported by Friebe and Gill (1994). Arm ratio (long/short) was calculated based on the mean of six homologous pairs of each chromosome as measured from enlarged photomicrographs. The results were compared with those reported by Endo and Gill (1994) and Landgeva et al. (1995). Whenever the mean arm ratio of a certain chromosome lied out of the range reported by these authors, Student's t-test was performed with its counterpart chromosome in SC.

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