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Karyotype and C‐Banding Patterns of Mitotic Chromosomes in Diploid Bromegrass (Bromus riparius Rehm)

Metin Tuna, Kulvinder Singh Gill, Kenneth P. Vogel

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Abstract

Previous cytogenetic studies of the genus Bromus L. were limited to chromosome counts and construction of karyotypes on the basis of Feulgen staining. Since the chromosomes of Bromus are similar in morphology, these karyotypes are of limited use for chromosome identification and genome analysis. The objectives of this study were to develop and evaluate a Giemsa C‐banding procedure to use in identification of individual bromegrass chromosomes and to develop a karyotype for diploid Bromus riparius Rehm. (2n = 14; PI 440215). All chromosomes had one or more C‐bands which were located mainly at telomeric regions. A group (I) of four pairs of chromosomes had telomeric bands on only one arm and could be differentiated. In this group, one pair had an interstitial C‐band along with a telomeric band, one pair had a nucleolus organizer region (NOR) at a subtelomeric location on the short arm, and the other two pair could be distinguished by centromere location. The other group (II) of three pairs of chromosomes had telomeric bands on both arms. The unequivocal identification of specific chromosomes of Group II was not possible in all cells because of their similarity and differential condensation of chromosomes. Chromosomes of both groups were either metacentric or submetacentric. The total length of individual chromosomes ranged from 5.58 to 6.87 μm and the arm ratios ranged from 1.02 to 1.5. The homologous chromosomes were paired and assigned numbers I to VII in decreasing length. A karyotype was constructed by means of the C‐bands, mean chromosome lengths, and arm ratios. The C‐banding procedure used in this study could be used to developed karyotypes for the other species of the genus Bromus and these C‐banded karyotypes could be used to compare genomes within the genus.

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What this paper is about

Previous cytogenetic studies of the genus Bromus L. were limited to chromosome counts and construction of karyotypes on the basis of Feulgen staining. Since the chromosomes of Bromus are similar in morphology, these karyotypes are of limited use for chromosome identification and genome analysis. The objectives of this study were to develop and evaluate a Giemsa C‐banding procedure to use in identification of individual bromegrass chromosomes and to develop a karyotype for diploid Bromus riparius Rehm. (2n = 14; PI 440215). All chromosomes had one or more C‐bands which were located mainly at telomeric regions. A group (I) of four pairs of chromosomes had telomeric bands on only one arm and could be differentiated. In this group, one pair had an interstitial C‐band along with a telomeric band, one pair had a nucleolus organizer region (NOR) at a subtelomeric location on the short arm, and the other two pair could be distinguished by centromere location. The other group (II) of three pairs of chromosomes had telomeric bands on both arms. The unequivocal identification of specific chromosomes of Group II was not possible in all cells because of their similarity and differential condensation of chromosomes. Chromosomes of both groups were either metacentric or submetacentric. The total length of individual chromosomes ranged from 5.58 to 6.87 μm and the arm ratios ranged from 1.02 to 1.5. The homologous chromosomes were paired and assigned numbers I to VII in decreasing length. A karyotype was constructed by means of the C‐bands, mean chromosome lengths, and arm ratios. The C‐banding procedure used in this study could be used to developed karyotypes for the other species of the genus Bromus and these C‐banded karyotypes could be used to compare genomes within the genus.

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Available abstract

Previous cytogenetic studies of the genus Bromus L. were limited to chromosome counts and construction of karyotypes on the basis of Feulgen staining. Since the chromosomes of Bromus are similar in morphology, these karyotypes are of limited use for chromosome identification and genome analysis. The objectives of this study were to develop and evaluate a Giemsa C‐banding procedure to use in identification of individual bromegrass chromosomes and to develop a karyotype for diploid Bromus riparius Rehm. (2n = 14; PI 440215). All chromosomes had one or more C‐bands which were located mainly at telomeric regions. A group (I) of four pairs of chromosomes had telomeric bands on only one arm and could be differentiated. In this group, one pair had an interstitial C‐band along with a telomeric band, one pair had a nucleolus organizer region (NOR) at a subtelomeric location on the short arm, and the other two pair could be distinguished by centromere location. The other group (II) of three pairs of chromosomes had telomeric bands on both arms. The unequivocal identification of specific chromosomes of Group II was not possible in all cells because of their similarity and differential condensation of chromosomes. Chromosomes of both groups were either metacentric or submetacentric. The total length of individual chromosomes ranged from 5.58 to 6.87 μm and the arm ratios ranged from 1.02 to 1.5. The homologous chromosomes were paired and assigned numbers I to VII in decreasing length. A karyotype was constructed by means of the C‐bands, mean chromosome lengths, and arm ratios. The C‐banding procedure used in this study could be used to developed karyotypes for the other species of the genus Bromus and these C‐banded karyotypes could be used to compare genomes within the genus.

Key concepts: Biology, Karyotype, Ploidy, Chromosome, Genetics, Centromere, Giemsa stain, Feulgen stain

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