Analysis of karyotypes and Giemsa C-banding patterns in eight species of Arachis

Genome ◽  
1987 ◽  
Vol 29 (1) ◽  
pp. 187-194 ◽  
Author(s):  
Q. Cai ◽  
S. Lu ◽  
C. C. Chinnappa
Keyword(s):  
Close Relationships ◽  
Diploid Species ◽  
Chromosome Morphology ◽  
Tetraploid Species ◽  
Interspecific Relationship ◽  
Banding Patterns ◽  
C Banding ◽  
B Genome ◽  
A Genome ◽  
Structural Differences

The karyotypes and Giemsa C-banding patterns of the chromosomes in eight species of Arachis L. have been studied. Six species are diploid with 20 chromosomes and two are tetraploid with 40 chromosomes. One diploid species (A. rigonii Krap. et Greg.) belongs to the sect. Erectoides and the rest belong to the sect. Arachis. Among the diploid species from the sect. Arachis, A. batizocoi Krap. et Greg, has a unique karyotype while others have similar karyotypes. Two tetraploid species, A. monticola Krap. et Greg, and A. hypogaea L., possess the most similar karyotypes. However, the diploid species, A. rigonii, from sect. Erectoides, has a karyotype distinguishable from those in sect. Arachis. The C-banding patterns of the chromosomes have been obtained for all the species. The centromeric bands have been found in all the chromosomes and the intercalary bands can be identified in a varied number of chromosomes among these complements. However, the telomeric bands only exist in one or two chromosomes. The comparison of banding patterns demonstrated that structural differences exist among the chromosomal complements of the species with similar chromosome morphology. The karyotype variation among the different species and interspecific relationship are discussed. It is suggested that all the diploid species with the A genome are closely related. There are close relationships between the tetraploid species and diploid species with the A or B genome within sect. Arachis. Key words: Arachis, cytology, karyotypes, Giemsa C-banding.

Characterization of genomes of timothy (Phleum pratense L.). I. Karyotypes and C-banding patterns in cultivated timothy and two wild relatives

Genome ◽  
1991 ◽  
Vol 34 (1) ◽  
pp. 52-58 ◽  
Author(s):  
Q. Cai ◽  
M. R. Bullen
Keyword(s):  
Phleum Pratense ◽  
Wild Relatives ◽  
Banding Patterns ◽  
C Banding ◽  
B Genome ◽  
A Genome ◽  
Cultivated Species ◽  
Genome Donors ◽  
Phleum Pratense L

In an attempt to know the phylogeny of timothy (Phleum pratense), the cultivated species and two wild relatives, Phleum alpinum and Phleum bertolonii, were karyotyped with conventional and Giemsa C-banding methods. In the hexaploid P. pratense (2n = 6x = 42), two sets of seven chromosomes were indistinguishable from each other both in morphology and in banding patterns and the third set of seven was found to be differentiated from them. Two genomes, A and B, were tentatively established. The banded karyotype in diploid P. alpinum (2n = 2x = 14) was close to the A genome, which was tetraploid in P. pratense, and the karyotype in P. bertolonii (2n = 2x = 14) was analogous to the B genome in P. pratense, which suggests these species were the genome donors of P. pratense.Key words: chromosome, genome, allopolyploid, Giemsa C-banding.

Giemsa C-banded karyotypes of Avena species

Genome ◽  
1988 ◽  
Vol 30 (5) ◽  
pp. 627-632 ◽  
Author(s):  
A. Fominaya ◽  
C. Vega ◽  
E. Ferrer
Keyword(s):  
Interspecific Hybrids ◽  
Chromatin Condensation ◽  
Diploid Species ◽  
Divergent Evolution ◽  
Intercalary Heterochromatin ◽  
Banding Patterns ◽  
Genome Species ◽  
C Banding ◽  
A Genome ◽  
C Genome

Giemsa C-banding was used to identify individual somatic chromosomes in eight diploid species of Avena. Two patterns of heterochromatin distribution were found. The chromosomes of five A genome species (A. strigosa, A. hirtula, A. longiglumis, A. damascena, and A. canariensis) possessed mainly telomeric bands, whereas those from three C genome species (A. clauda, A. pilosa, and A. ventricosa) were characterized by higher chromatin condensation and several intercalary heterochromatin bands. The divergent evolution between the two groups is confirmed after C-banding. The unique C-banding patterns of several chromosomes in each species will be a useful tool for the study of meiotic behaviour in interspecific hybrids among Avena spp.Key words: C-banding, Avena, heterochromatin.

C-banding and nucleolar activity of tetraploid Avena species

Genome ◽  
1988 ◽  
Vol 30 (5) ◽  
pp. 633-638 ◽  
Author(s):  
A. Fominaya ◽  
C. Vega ◽  
E. Ferrer
Keyword(s):  
Diploid Species ◽  
Nucleolar Organizer ◽  
Nucleolar Organizer Regions ◽  
Good Correspondence ◽  
Banding Patterns ◽  
Genome Species ◽  
Nucleolar Activity ◽  
C Banding ◽  
A Genome ◽  
Nucleolar Organizer Activity

The Giemsa C-banding pattern of the chromosomes of five tetraploid species of Avena have been studied. The chromosomes of AABB species (A. barbata, A. vaviloviana, and A. abyssinica) had similar C-banding patterns to those of A genome species. AACC species (A. maroccana and A. murphyi) possessed two sets of seven chromosome pairs with C-banding patterns similar to those observed in the diploid A and C genome species. However, no good correspondence between either of these two chromosome groups and any one diploid species has been found. When the nucleolar organizer activity of the species was analysed by silver staining, fewer nucleoli and nucleolar organizer regions (NORs) were observed than expected, assuming complete additivity of those from the donor diploid species.Key words: C-banding, NOR, Avena, 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.

Chromosomal localization and characterization of rDNA loci in the Brassica A and C genomes

Genome ◽  
1997 ◽  
Vol 40 (4) ◽  
pp. 582-587 ◽  
Author(s):  
R. J. Snowdon ◽  
W. Köhler ◽  
A. Köhler
Keyword(s):  
In Situ Hybridization ◽  
Fluorescence In Situ Hybridization ◽  
Ribosomal Dna ◽  
Diploid Species ◽  
Rdna Locus ◽  
Chromosome Morphology ◽  
Rdna Site ◽  
A Genome ◽  
Rdna Loci

Using fluorescence in situ hybridization, we located ribosomal DNA loci on prometaphase chromosomes of the diploid species Brassica rapa and Brassica oleracea and their amphidiploid Brassica napus. Based on comparisons of chromosome morphology and hybridization patterns, we characterized the individual B. napus rDNA loci according to their presumed origins in the Brassica A and C genomes. As reported in other studies, the sum of rDNA loci observed on B. rapa (AA genome) and B. oleracea (CC genome) chromosomes was one greater than the total number of loci seen in their amphidiploid B. napus (AACC). Evidence is presented that this reduction in B. napus rDNA locus number results from the loss of the smallest A genome rDNA site in the amphidiploid.Key words: Brassica, fluorescence in situ hybridization, ribosomal DNA, rDNA.

The origin of wheat chromosomes 4A and 4B and their genome reallocation

1983 ◽  
Vol 25 (3) ◽  
pp. 210-214 ◽  
Author(s):  
J. Dvořák
Keyword(s):  
Triticum Aestivum ◽  
Banding Pattern ◽  
The Other ◽  
Evolutionary Lineage ◽  
C Banding ◽  
B Genome ◽  
A Genome

Triticum aestivum chromosome "4A" is, like the B genome chromosomes, extensively heterochromatic while the remaining six A genome chromosomes are not. In the presence of the Ph gene it does not pair with any chromosome of einkorn wheats, T. monococcum and T. urartu, the source of the A genome. It is shown here that the same chromosome is also present in T. timopheevii which represents the other evolutionary lineage of wheats. The "4A" chromosomes of T. timopheevii and T. aestivum pair poorly with each other, like the B genome chromosomes of the two lineages, while the remaining A genome chromosomes, except for one arm, pair relatively well. Hence, in both lineages chromosome "4A" has the attributes of the B genome chromosomes, not of the A genome chromosomes. The C-banding pattern of chromosome "4A" of T. aestivum and T. timopheevii closely resembles the C-banding pattern of a chromosome of T. speltoides and less closely chromosome 4B1 of T. sharonense. On the basis of this and other evidence it is concluded that this chromosome was contributed by a species of the section Sitopsis and, consequently, belongs to the B genome. Additionally, there is evidence that the chromosome that was originally designated "4B" belongs to the A genome.

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.

A AND B GENOME HOMOEOLOGIES IN TETRAPLOID AND OCTOPLOID CYTOTYPES OF BROMUS INERMIS

1979 ◽  
Vol 21 (1) ◽  
pp. 65-71 ◽  
Author(s):  
K. C. Armstrong
Keyword(s):  
Chromosome Pairing ◽  
Convincing Evidence ◽  
Bromus Inermis ◽  
Open Pollination ◽  
Homoeologous Chromosome ◽  
Genome Chromosome ◽  
B Genome ◽  
Homoeologous Chromosome Pairing ◽  
A Genome ◽  
Structural Differences

Homoeology between the A and B genomes of allotetraploid (2n = 4x = 28) AiAiBiBi and autoallooctoploid (2n = 8x = 56) AIAIAIAIBIBIBIBI cytotypes of B. inermis Leyss. was studied in a tetraploid F1 hybrid (AeAeAiBi) from 4x B. erectus × 4x B. inermis and in a haplo-triploid (AIeAIeBI) which occurred spontaneously in the F2 from open-pollination among plants of the hexaploid F1 hybrid (AeAeAIAIBIBI) from 4x B. erectus × 8x B. inermis. Chromosome pairing at metaphase I in both the tetraploid (AeAeAiBi) and haplo-triploid (AIeAIeBI) indicated that for each A genome chromosome there was a corresponding B genome homoeologue. There was no convincing evidence of gross structural differences between the two homoeologous genomes. The frequency of trivalent formation in the haplo-triploid was approximately one-half that found in two pentaploids (2n = 5x = 35) AIeAIeAIBIBI. This indicates that the pairing affinity between the A and B genomes is one-half that between homologues as expressed by trivalent formation in triploids of the type AAB and AAA. Homoeologous chromosome pairing (A with B) may be controlled by a gene which is hemizygous ineffective.

scholarly journals Pervasive hybridizations in the history of wheat relatives

2018 ◽  
Author(s):  
Sylvain Glémin ◽  
Celine Scornavacca ◽  
Jacques Dainat ◽  
Concetta Burgarella ◽  
Véronique Viader ◽  
...  
Keyword(s):  
Methodological Approach ◽  
Diploid Species ◽  
Phylogenomic Analysis ◽  
D Genome ◽  
Species Relationship ◽  
B Genome ◽  
Hybridization Event ◽  
A Genome ◽  
History Of ◽  
Complex Scenario

AbstractBread wheat and durum wheat derive from an intricate evolutionary history of three genomes, namely A, B and D, present in both extent diploid and polyploid species. Despite its importance for wheat research, no consensus on the phylogeny of the wheat clade has emerged so far, possibly because of hybridizations and gene flows that make phylogeny reconstruction challenging. Recently, it has been proposed that the D genome originated from an ancient hybridization event between the A and B genomes1. However, the study only relied on four diploid wheat relatives when 13 species are accessible. Using transcriptome data from all diploid species and a new methodological approach, we provide the first comprehensive phylogenomic analysis of this group. Our analysis reveals that most species belong to the D-genome lineage and descend from the previously detected hybridization event, but with a more complex scenario and with a different parent than previously thought. If we confirmed that one parent was the A genome, we found that the second was not the B genome but the ancestor of Aegilops mutica (T genome), an overlooked wild species. We also unravel evidence of other massive gene flow events that could explain long-standing controversies in the classification of wheat relatives. We anticipate that these results will strongly affect future wheat research by providing a robust evolutionary framework and refocusing interest on understudied species. The new method we proposed should also be pivotal for further methodological developments to reconstruct species relationship with multiple hybridizations.

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