Differential chromosomal stainings for various species belonging to genera in the tribe Cricetini of the Eurasian Cricetinae including Cricetus, Cricetulus, Tscherskia, Phodopus, and Mesocricetus are available (Gamperl et al. 1978; Kartavtseva et al. 1979; Popescu and DiPaolo 1980; Kral et al. 1984). Hitherto, however, no differential chromosomes stainings for species in the genus Allocricetulus have been described and the phylogenetic position of this genus in the Cricetini, based on chromosomal data, has not been determined. The Eversmann’s hamster Allocricetus eversmanni Brandt, 1859 occurs in dry steppes and semi-deserts between the Volga and Ural rivers in Russia and in Kazakhstan, and includes three subspecies. The karyotype of A. eversmanni (2n = 26) was first described by Matthey (1960) from Kazakhstan, then subsequently those for subspecies, A. e. eversmanni and A. e. beljaevi (2n = 26, NF = 40: 8M + 10T + 6ST, X – SM, Y – SM) and A. e. pseudocurtatus (2n = 26; NF = 38: 8M + 12T + 4ST, X – M/SM, Y – SM/ST) were described. Kartavtseva and Vorontsov (1992) found distinctions in the morphology of one pair of large autosomes, pair no. 5, and in the size and morphology of the Y-chromosome and have suggested that the difference in the chromosome pair no. 5 appeared in A. e. pseudocurtatus. One female A. e. eversmanni was captured in the vicinity of Djakovka Village, Saratov Region, near the Lower Volga River, Russia. Chromosome preparations were obtained from bone marrow cells. After colcemidtreatment and hypotonic treatment with KCl-solution, the cells were fixed with acetic-methanol (1 : 3) and air or flame-dried. We arranged the chromosomes as described previously by Kartavtseva and Vorontsov (1992). The procedure of tripsin treatment was used for G-banding (Seabright 1971). The distribution of heterochromatin in chromosomes was shown using Sumner’s (1972) modified C-banding technique. The locations of nucleolar organizer regions (NORs) of metaphase chromosomes were determined after 50% aqueous AgNO3 treatment for 12 hours at 50–60°C (Bloom and Goodpasture 1976). The karyotype consisted of 24 autosomes (2n = 26, NF = 40): four pairs of metacentrics (M) and submetacentrics (SM): one pair large, one pair medium and two pairs small, two pairs of large subtelocentrics (ST) and six pairs of acrocentrics (A), ranging from medium-sized to small. The X chromosome was a medium sized submetacentric (Fig. 1). Differential G-staining made it possible to define the homologues in the karyotype (Fig. 1a). The short arm of the large subtelocentric no. 5 had no clear bands, while the short arm of the large subtelocentric no. 6 had a clear band in the pericentromeric region. The least acrocentrics nos. 11 and 12 had no clear bands. The C-staining of chromosomes obtained a low amount of heterochromatin in A. e. eversmanni in biarmed chromosomes nos. 1, 2, 5, 6, and acrocentric no. 7 had no positive band. The two pairs of small metacentrics nos. 3, 4 and small acrocentrics nos. 8–12 had heterochromatin in pericentromeric areas. The X chromosome carried one dark C-block in the pericentromeric region of the short arm (Fig. 1b). NORs were ascertained in five pairs of chromosomes. In pairs 2, 4, and 5 of biarmed chromosomes, the NORs were found at the telomeric ends (pair 5 had NORs in short arms). In the acrocentric pairs 8 and 10, very small NORs were observed at the centromeric positions (Fig. 1c). Earlier we assumed that distinction among A. e. eversmanni, A. e. beljaevi and A. e. pseudocurtatus based on the occurrence of deletion in the short arm of
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Sep 1, 2013
Reza Yadollahvand + 2
Open Access