scholarly journals C-banding Patterns in Somatic and Meiotic Chromosomes of Crepis capillaris

1977 ◽  
Vol 53 (1) ◽  
pp. 6-9 ◽  
Author(s):  
Ryuso TANAKA ◽  
Hiroko KOMATSU
Keyword(s):  
Banding Patterns ◽  
Crepis Capillaris ◽  
C Banding ◽  
Meiotic Chromosomes

Rye C-banding patterns and meiotic stability of hexaploid triticale (× Triticosecale) selections differing in kernel shriveling

Genome ◽  
1990 ◽  
Vol 33 (5) ◽  
pp. 686-689 ◽  
Author(s):  
Charles M. Papa ◽  
R. Morris ◽  
J. W. Schmidt
Keyword(s):  
Secale Cereale ◽  
Chromosome Banding ◽  
Agronomic Performance ◽  
Hexaploid Triticale ◽  
Kernel Development ◽  
Banding Patterns ◽  
C Banding ◽  
Meiotic Stability ◽  
Metaphase I

Two winter hexaploid triticale populations derived from the same cross were selected on the basis of grain appearance and agronomic performance. The five lines from 84LT402 showed more kernel shriveling than the four lines from 84LT401. The derived lines were analyzed for aneuploid frequencies, rye chromosome banding patterns, and meiotic stability to detect associations with kernel development. The aneuploid frequencies were 16% in 84LT401 and 18% in 84LT402. C-banding showed that both selection groups had all the rye chromosomes except 2R. The two groups had similar telomeric patterns but differed in the long-arm interstitial patterns of 4R and 5R. Compared with lines from 84LT402, those from 84LT401 had significantly fewer univalents and rod bivalents, and more paired arms at metaphase I; fewer laggards and bridges at anaphase I; and a higher frequency of normal tetrads. There were no significant differences among lines within each group for any meiotic character. Since there were no differences within or between groups in telomeric banding patterns, the differences in kernel shriveling and meiotic stability might be due to genotypic factors and (or) differences in the interstitial patterns of 4R and 5R. By selecting plump grains, lines with improved kernel characteristics along with improved meiotic stability are obtainable.Key words: triticale, meiotic stability, C-banding, Secale cereale, heterochromatin.

Cytological identification of some trisomics of Russian wildrye (Psathyrostachys juncea)

Genome ◽  
1995 ◽  
Vol 38 (6) ◽  
pp. 1271-1278 ◽  
Author(s):  
Jun-Zhi Wei ◽  
W. F. Campbell ◽  
G. J. Scoles ◽  
A. E. Slinkard ◽  
R. Ruey-Chyi Wang
Keyword(s):  
Crop Improvement ◽  
Diploid Species ◽  
Pollen Grains ◽  
Morphological Characters ◽  
Cereal Crop ◽  
Banding Patterns ◽  
C Banding ◽  
Psathyrostachys Juncea ◽  
Double Deletion ◽  
Russian Wildrye

Russian wildrye, Psathyrostachys juncea (Fisch.) Nevski (2n = 2x = 14; NsNs), is an important forage grass and a potential source of germplasm for cereal crop improvement. Because of genetic heterogeneity as a result of its self-incompatibility, it is difficult to identify trisomics of this diploid species based on morphological characters alone. Putative trisomies (2n = 2x + 1 = 15), derived from open pollination of a triploid plant by pollen grains of diploid plants, were characterized by Giemsa C-banding. Based on both karyotypic criteria and C-banding patterns, four of the seven possible primary trisomics, a double-deletion trisomic, and two tertiary trisomics were identified.Key words: Russian wildrye, Psathyrostachys juncea, trisomic, C-banding, karyotype.

Giemsa C-banded karyotypes of Hordeum marinum and H. murinum

Genome ◽  
1989 ◽  
Vol 32 (4) ◽  
pp. 629-639 ◽  
Author(s):  
Ib Linde-Laursen ◽  
Roland von Bothmer ◽  
Niels Jacobsen
Keyword(s):  
Chromosome Morphology ◽  
Similar Distribution ◽  
Banding Patterns ◽  
Homologous Chromosomes ◽  
C Banding ◽  
Linear Relationships ◽  
Close Relationship ◽  
Different Populations ◽  
Pattern Polymorphism ◽  
Hordeum Species

Giemsa C-banding patterns of the predominantly self-pollinating, annual species Hordeum marinum (2x, 4x) and H. murinum (2x, 4x, 6x) showed mostly very small to small bands at centromeric and telomeric positions, at one or both sides of the nucleolar constrictions, and at intercalary positions with no preferential disposition. A similar distribution of bands has been observed in other Hordeum species, suggesting that the pattern is the basic one in the genus Hordeum. Hordeum murinum, especially the hexaploid cytotype, was distinguished from H. marinum by having more numerous and more conspicuous bands, resulting in a significantly higher percentage of constitutive heterochromatin (9–17 vs. 4–8%). The differences in C-banding patterns supported by differences in chromosome morphology confirm that H. marinum and H. murinum are not closely related. Banding-pattern polymorphism was prevalent among populations but unobserved within populations. In spite of this polymorphism, banding patterns in combination with chromosome morphology identified homologous chromosomes of different populations of a taxon and indicated that the chromosome complements of the polyploids of both species comprised the genome of the related diploid as well as one or two "unidentified" genomes. This agrees with an alloploid origin of polyploids. The C-banding patterns of H. marinum ssp. marinum and H. marinum ssp. gussoneanum (2x) showed some divergence in spite of the close relationship. The C-banded karyotypes of H. murinum ssp. murinum and H. murinum ssp. leporinum (4x) were very similar, supporting conspecificity. Chromosome lengths and longest/shortest chromosome ratios were fairly similar to those previously published, supporting the conclusion that linear relationships of chromosomes are normally stable within genomes. The taxonomy of the two species is discussed.Key words: C-banding, karyotypes, Hordeum.

CHROMOSOME BANDING HOMOLOGIES OF A TANDEM FUSION IN RIVER, SWAMP, AND CROSSBRED BUFFALOES (BUBALUS BUBALIS)

1982 ◽  
Vol 24 (6) ◽  
pp. 667-673 ◽  
Author(s):  
T. A. Bongso ◽  
M. Hilmi
Keyword(s):  
First Generation ◽  
Bubalus Bubalis ◽  
Chromosome 9 ◽  
Chromosome 4 ◽  
Centromere Region ◽  
Hybrid Female ◽  
Banding Patterns ◽  
C Banding ◽  
Tandem Fusion ◽  
Y Chromosomes

The chromosomes of the Murrah (River), Swamp (Malaysian kerbau), F1 hybrid (Murrah × Swamp) and first generation backcross (F1 hybrid female × Murrah male) buffaloes (Bubalus bubalis L.) were studied using Giemsa (G) and centromeric (C) banding techniques. The diploid chromosome number for the Murrah was 2n = 50, Swamp 2n = 48, F1 hybrid 2n = 49 and two backcross animals had 2n = 49 and 2n = 50, respectively. The largest two metacentric chromosomes of the Swamp resulted from a tandem fusion between the two chromosomes 4p and 9, respectively, of the Murrah karyotype. The F1 hybrid (2n = 49) and one of the backcrosses (2n = 49) had karyotypes intermediate to the Murrah and Swamp parents. The C banding patterns were useful in identifying the X and Y chromosomes of the buffalo and demonstrated that a major portion of the centromere region of chromosome 9 was not incorporated into chromosome 4 during the tandem fusion.

C-banding patterns and phenotypic characteristics in individuals ofSapajus(Primates: Platyrrhini) and its application to management in captivity

Caryologia ◽  
2014 ◽  
Vol 67 (4) ◽  
pp. 314-320
Author(s):  
Diego Mattos Penedo ◽  
Jorge Luís Azevedo de Armada ◽  
José Francisco Santos da Silva ◽  
Daniel Marchesi Neves ◽  
Alcides Pissinatti ◽  
...  
Keyword(s):  
Phenotypic Characteristics ◽  
Banding Patterns ◽  
C Banding ◽  
In Captivity

Chromosome C-banding patterns in Spanish Acridoidea

Genetica ◽  
1983 ◽  
Vol 61 (1) ◽  
pp. 65-74 ◽  
Author(s):  
J. L. Santos ◽  
P. Arana ◽  
R. Gir�ldez
Keyword(s):  
Banding Patterns ◽  
C Banding

Intergeneric hybridization and C-banding patterns inHordelymus (Triticeae, Poaceae)

1994 ◽  
Vol 189 (3-4) ◽  
pp. 259-266 ◽  
Author(s):  
Roland von Bothmer ◽  
Bao-Rong Lu ◽  
Ib Linde-Laursen
Keyword(s):  
Intergeneric Hybridization ◽  
Banding Patterns ◽  
C Banding

Genetic and cytogenetic analyses of the A genome of Triticum monococcum. VI. Production and identification of primary trisomics using the C-banding technique

Genome ◽  
1990 ◽  
Vol 33 (4) ◽  
pp. 542-555 ◽  
Author(s):  
B. Friebe ◽  
N.-S. Kim ◽  
J. Kuspira ◽  
B. S. Gill
Keyword(s):  
Nucleolus Organizer ◽  
Triticum Monococcum ◽  
Banding Patterns ◽  
Primary Trisomics ◽  
Nucleolus Organizer Regions ◽  
C Banding ◽  
A Genome ◽  
Chromosome 5A ◽  
Triple Dose

Cytogenetic studies in Triticum monococcum (2n = 2x = 14) are nonexistent. To initiate such investigations in this species, a series of primary trisomics was generated from autotriploids derived from crosses between induced autotetraploids and diploids. All trisomics differed phenotypically from their diploid progenitors. Only two of the seven possible primary trisomic types produced distinct morphological features on the basis of which they could be distinguished. The chromosomes in the karyotype were morphologically very similar and could not be unequivocally identified using standard techniques. Therefore, C-banding was used to identify the chromosomes and trisomics of this species. Ag–NOR staining and in situ hybridization, using rDNA probes, were used to substantiate these identifications. A comparison of the C-banding patterns of the chromosomes of T. monococcum with those of the A genome in Triticum aestivum permitted identification of five of its chromosomes, viz., 1A, 2A, 3A, 5A, and 7A. The two remaining chromosomes possessed C-banding patterns that were not equivalent to those of any of the chromosomes in the A genome of the polyploid wheats. When one of these undesignated chromosomes from T. monococcum var. boeoticum was substituted for chromosome 4A of Triticum turgidum, it compensated well phenotypically and therefore genetically for the loss of this chromosome in the recipient species. Because this T. monococcum chromosome appeared to be homoeologous to the group 4 chromosomes of polyploid wheats, it was designated 4A. By the process of elimination the second undesignated chromosome in T. monococcum must be 6A. Analysis of the trisomics obtained led to the following conclusions. (i) Trisomics for chromosome 3A were not found among the trisomic lines analyzed cytologically. (ii) Primary trisomics for chromosomes 2A, 4A, 6A, and 7A were positively identified. (iii) Trisomics for the SAT chromosomes 1A and 5A were positively identified in some cases and not in others because of polymorphism in the telomeric C-band of the short arm of chromosome 1A. (iv) Trisomics for chromosome 7A were identified on the basis of their distinct phenotype, viz., the small narrow heads and small narrow leaves. Because rRNA hybridizes lightly to nucleolus organizer regions on chromosome 1A and heavily to nucleolus organizer regions on chromosome 5A, our results indicate that trisomics in line 50 carry chromosome 1A in triple dose and trisomics in lines 28 and 51 carry chromosome 5A in triplicate. Variable hybridization of the rDNA probe to nucleolus organizer regions on chromosomes in triple dose in lines 7, 20, and 28 precluded the identification of the extra chromosome in these lines. Cytogenetic methods for unequivocally identifying trisomics for chromosomes 1A and 5A are discussed. Thus six of the series of primary trisomics have been identified. Telotrisomic lines are also being produced.Key words: Triticum monococcum, trisomics, C-banding, Ag-NOR staining, in situ hybridization, rDNA probes, plant morphology.

Characterization of the canine karyotype by counterstain-enhanced chromosome banding

1983 ◽  
Vol 25 (6) ◽  
pp. 616-621 ◽  
Author(s):  
B. Mayr ◽  
D. Schweizer ◽  
W. Schleger
Keyword(s):  
Actinomycin D ◽  
Mitotic Division ◽  
Banding Technique ◽  
Chromosome Identification ◽  
Banding Patterns ◽  
Distamycin A ◽  
Fluorescent Banding ◽  
Meiotic Chromosomes ◽  
Triple Staining

The application of the counterstain-contrasted fluorescent banding technique to canine chromosomes provided an improved capability to highlight specific heterochromatic regions and to produce well defined banding patterns both on mitotic and meiotic chromosomes. Triple staining with chromomycin A3 – distamycin A – DAPI revealed the occurrence of DA – DAPI positive heterochromatin in chromosomes 33, 36, 37, and 38. Pachytene nuclei present more favourable material for the detection of very small amounts of DA – DAPI material than mitotic division stages. Counterstain-enhanced chromomycin R-banding greatly facilitated chromosome identification. A standard R-band karyotype of Canis familiaris is proposed and described in some detail. DAPI – actinomycin D staining produced a QFH-type banding pattern and enhanced differentiation of some polymorphic regions.

Variability of C-banding patterns in Japanese quail chromosomes

Genome ◽  
1991 ◽  
Vol 34 (6) ◽  
pp. 993-997 ◽  
Author(s):  
C. A. de la Seña ◽  
N. S. Fechheimer ◽  
K. E. Nestor
Keyword(s):  
Japanese Quail ◽  
Centromeric Region ◽  
Terminal Region ◽  
Z Chromosome ◽  
W Chromosome ◽  
Chromosome 4 ◽  
Banding Patterns ◽  
Chromosome Markers ◽  
C Banding

Observations were made of the C-banding patterns in several cells from 182 Japanese quail embryos to detect presence of stable variants. Each of the eight largest autosomes contains a C-band at the centromeric region. The short arm of autosome 8 is C-band positive, as is the entire W chromosome. The Z chromosome consistently contains an interstitial C-band in the long arm and a less prominent one in the short arm. Distinct variants of chromosome 4 and the Z chromosome were observed. In the Z chromosome a C-band at the terminal region of the short arm was markedly elongated in some embryos. Likewise, the short arm of chromosome 4 was much more prominent in one or both of the homologues in some embryos. Most of the microchromosomes contain a prominent C-band. The heteromorphisms are useful chromosome markers to detect the origins of heteroploidy in early embryos.Key words: C-band variants, Japanese quail, Coturnix.

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