Identification of a barley chromosomal interchange using N-banding and in situ hybridization techniques

Genome ◽  
1992 ◽  
Vol 35 (3) ◽  
pp. 392-397 ◽  
Author(s):  
Jie Xu ◽  
K. J. Kasha
Keyword(s):  
In Situ Hybridization ◽  
Rapid Identification ◽  
Root Tip ◽  
Chromosome 4 ◽  
Chromosome Identification ◽  
Chromosomal Interchange ◽  
Mother Cells ◽  
Tip Cells ◽  
Root Tip Cells

The combination of N-banding and in situ hybridization was used to illustrate the rapid identification of the chromosomes involved in a newly formed chromosomal interchange (reciprocal translocation) in barley. The plant heterozygous for the interchange was derived from the backcross of 'Su Pie', a two-rowed Chinese winter barley cultivar (2n = 2x = 14), with pollen from a triploid interspecific F1 hybrid (2n = 3x = 21) obtained from the cross of 'Su Pie' × tetraploid Hordeum bulbosum accession GBC141 (2n = 4x = 28). Pollen mother cells of the interchanged plant exhibited one quadrivalent and five bivalents in 97.8% of cells. Partial sterility of florets was observed in spikes obtained from self-pollination and the plants morphologically resembled barley. Barley chromosomes were readily identified by N-banding from root-tip cells with one band missing from the short arm of one of the pair of chromosome 4. N-banding of metaphase I of meiosis revealed that chromosomes 1, 2, and 5 were not involved in the interchange. In situ hybridization with a rDNA probe showed that chromosomes 6 and 7 were paired as bivalents. In conclusion, chromosomes 3 and 4 are involved in the interchange with the breakpoint in the short arm of chromosome 4 between the two proximal N-bands. The use of chromosome-specific DNA probes for chromosome identification using in situ hybridization is proposed.Key words: barley, chromosomal interchange, N-banding, in situ hybridization, rDNA.

Mitotic and meiotic irregularities in somatic hybrids of Lycopersicon esculentum and Solanum tuberosum

Genome ◽  
1994 ◽  
Vol 37 (5) ◽  
pp. 726-735 ◽  
Author(s):  
A. M. A. Wolters ◽  
H. C. H. Schoenmakers ◽  
S. Kamstra ◽  
J. van Eden ◽  
M. Koornneef ◽  
...  
Keyword(s):  
In Situ Hybridization ◽  
High Frequency ◽  
Somatic Hybrids ◽  
Unreduced Gametes ◽  
Root Tip ◽  
Root Tips ◽  
Tetrad Stage ◽  
Chromosome Arm ◽  
Mother Cells

Chromosome numbers were determined in metaphase complements of root-tip meristems of 107 tomato (+) potato somatic hybrids, obtained from five different combinations of parental genotypes. Of these hybrids 79% were aneuploid, lacking one or two chromosomes in most cases. All four hybrids that were studied at mitotic anaphase of root tips showed laggards and bridges, the three aneuploids in a higher frequency than the single euploid. Hybrid K2H2-1C, which showed the highest percentage of aberrant anaphases, possessed 46 chromosomes. Fluorescence in situ hybridization with total genomic DNA showed that this hybrid contained 23 tomato, 22 potato, and 1 recombinant chromosome consisting of a tomato chromosome arm and a potato chromosome arm. The potato parent of K2H2-1C was aneusomatic in its root tips with a high frequency of monosomic and trisomic cells and a relatively high frequency of cells with one fragment or telosome. Meiotic analyses of three tomato (+) potato somatic hybrids revealed laggards, which occurred most frequently in the triploid hybrids, and bridges, which were frequently present in pollen mother cells (PMCs) at anaphase I of hypotetraploid K2H2-1C. We observed putative trivalents in PMCs at diakinesis and metaphase I of eutriploid A7-82A and quadrivalents in part of the PMCs of hypotetraploid K2H2-1C, suggesting that homoeologous recombination between tomato and potato chromosomes occurred in these hybrids. All three hybrids showed a high percentage of first division restitution, giving rise to unreduced gametes. However, shortly after the tetrad stage all microspores completely degenerated, resulting in exclusively sterile pollen.Key words: tomato, potato, symmetric somatic hybrids, chromosomal irregularities, genomic in situ hybridization.

CYTOGENETICS OF 6X-AMPHIPLOID × AVENA SATIVA L. F1 HYBRIDS

1971 ◽  
Vol 13 (2) ◽  
pp. 292-297 ◽  
Author(s):  
R. A. Forsberg ◽  
S. Wang
Keyword(s):  
Avena Sativa ◽  
Seed Set ◽  
Pollen Grains ◽  
F1 Hybrids ◽  
Root Tip ◽  
Ploidy Levels ◽  
Sperm Nuclei ◽  
Mother Cells ◽  
Tip Cells ◽  
Root Tip Cells

Avena abyssinica (2n=28) × A. strigosa (2n=14) 6x amphiploids were crossed with 13 different A. sativa (2n=42) varieties or selections. There was considerable variation in chromosome number within and among F1 plants. The mode was 40 in root tip cells and 41 in pollen mother cells (PMC's). The number of univalents in PMC's ranged from 10 to 27 with a mean of 18.9. The average number of bivalents was 7.1, ranging from 2 to 13. Multiple associations were common. Only 10.8% of the pollen grains contained normally developed nuclei, i.e. one vegetative and two elongated sperm nuclei. Forty of 41 F1 plants were completely self-sterile and only one seed was obtained from 16,950 florets. Seed set in backcross pollinations with A. sativa was 1.25%, providing some opportunity for perpetuation of desirable genes from lower ploidy levels.

An advanced generation of Aranda orchids

Genome ◽  
1988 ◽  
Vol 30 (4) ◽  
pp. 608-611 ◽  
Author(s):  
Y. H. Lee ◽  
F. Y. Tham
Keyword(s):  
Somatic Chromosome ◽  
Intergeneric Hybrids ◽  
Root Tip ◽  
Chromosome Counts ◽  
Pollen Mother Cells ◽  
Mother Cells ◽  
Tip Cells ◽  
Somatic Chromosome Numbers ◽  
Root Tip Cells ◽  
Advanced Generation

Aranda orchids are a group of artificially bred intergeneric hybrids between member species (2n = 38) of two natural genera, Vanda and Arachnis, of Orchidaceae. Nine second generation Aranda cultivars were selected for analysis of somatic chromosome numbers, meiotic behaviour, and sporad formation. Eight of the cultivars were derived from Aranda × Vanda crosses and one from an Aranda × Aranda cross. Chromosome counts of their root tip cells showed that eight of them contained 2n = 3x = 57 chromosomes each, presumably resulting from unreduced eggs of the Aranda parent fertilized by haploid Vanda pollen. The ninth revealed 2n = 2x = 38 chromosomes. Pollen mother cells of eight of the cultivars (2n = 3x = 57) commonly formed more than 10 bivalents, presumably between homologous Vanda chromosomes, as well as many univalents, mainly of Arachnis chromosomes. Only 8–10 bivalents were observed in pollen mother cells of the ninth cultivar (2n = 2x = 38). All the cultivars formed a range of dyads containing unreduced microspores. Two mechanisms are proposed for the origin of these dyad sporads.Key words: Aranda orchids, intergeneric hybrids, cytology.

scholarly journals Cytogenetics of Mimosa bimucronata (DC.) O. Kuntze (Mimosoideae, Leguminosae): chromosome number, polysomaty and meiosis

2011 ◽  
Vol 11 (1) ◽  
pp. 27-36 ◽  
Author(s):  
Denise Olkoski ◽  
Maria Teresa Schifino Wittmann
Keyword(s):  
Seed Set ◽  
Pollen Grains ◽  
Root Tip ◽  
Rio Grande Do Sul ◽  
Root Tips ◽  
Pollen Mother Cells ◽  
Species Area ◽  
Mother Cells ◽  
Tip Cells ◽  
Root Tip Cells

Chromosome numbers (somatic and/or gametic) were determined in 50 populations of M. bimucronata (DC.) O. Kuntze collected in the species area of distribution in Rio Grande do Sul, south Brazil. All populations were diploid (2n = 2x = 26, n = 13). Polysomatic (mostly tetraploid) cells were detected in the seedlings root-tip cells in 39 out of the 41 populations examined, ranging from 3.0 to 28.2 % among populations, but were absent in the root-tips of grown plants. Polysomaty was as well absent in pollen-mother cells. In M. bimucronata pollen-mother cells are joined two-by-two before the onset of meiosis, remaining attached during all the meiotic division until the formation of pollen grain polyads, composed of two sets of four pollen grains each, that are dispersed in this way, which, according to previous suggestions would be an adaptation to ensure high seed set after a single pollination event.

scholarly journals PROGRESS IN THE DEVELOPMENT OF A MENTHA GERMPLASM COLLECTION

HortScience ◽  
1991 ◽  
Vol 26 (6) ◽  
pp. 774D-774
Author(s):  
Henrietta L. Chambers ◽  
Barbara M. Reed ◽  
Joseph D. Postman ◽  
Kim Hummer
Keyword(s):  
Bacterial Contamination ◽  
Germplasm Collection ◽  
In Vitro Cultures ◽  
F1 Hybrids ◽  
Root Tip ◽  
Meristem Culture ◽  
Mother Cells ◽  
Tip Cells ◽  
Root Tip Cells

Approximately 450 accessions representing 40 taxa from around the world, including 77 advanced breeder selections and 54 F1 hybrids are maintained at the repository in Corvallis. Most of the clones came from the collection of M. J. Murray of the A. M. Todd Company, Kalamazoo, MI. Others were received from the former USDA/ARS mint breeding program in Corvallis which ended in 1981. Data on origin, morphology, pedigree, oil analysis, fertility and chromosome number was provided with many of the accessions. We have confirmed the identity of the clones utilizing many of these features. We are actively seeking unrepresented germplasm. Chromosomes from pollen mother cells or root-tip cells are currently being counted. Nomenclature changes reflecting recent research have been made. Many clones have been indexed for viruses. Infected clones are treated with thermotherapy and meristem culture to produce virus-negative replacements. An in vitro backup collection is maintained in cold storage. Iniation of in vitro cultures has been complicated by internal bacterial contamination in some clones. Research to eliminate this problem is in progress. Cuttings and in vitro cultures of Mentha germplasm are available to researchers worldwide.

C-banding and fluorescence in situ hybridization studies of the wheat–alien hybrid 'Agrotana'

Genome ◽  
1994 ◽  
Vol 37 (3) ◽  
pp. 477-481 ◽  
Author(s):  
Jie Xu ◽  
R. L. Conner ◽  
A. Laroche
Keyword(s):  
In Situ Hybridization ◽  
Fluorescence In Situ Hybridization ◽  
Genomic Dna ◽  
Chromosome Engineering ◽  
C Banding ◽  
Chinese Spring Wheat ◽  
Mother Cells ◽  
Alien Chromatin ◽  
Chromosome Segments

'Agrotana', a wheat-alien hybrid (2n = 56), is a potential source of resistance to common root rot, stem rust, wheat streak mosaic virus, and the wheat curl mite. However, the origin of 'Agrotana', reported to be durum wheat × Agropyron trichophorum (pubescent wheatgrass), is uncertain. The objective of this investigation was to determine the chromosome constitution of 'Agrotana' using C-banding and fluorescence in situ hybridization techniques. The F1 hybrid of 'Agrotana' × 'Chinese Spring' wheat showed 7 I + 21 II in 14.9% of the pollen mother cells, evidence of the presence of the A, B, and D genomes in 'Agrotana'. The hybrid had 16 heavily C-banded chromosomes, namely 4A, and 1-7B of wheat, and a translocation that probably involved wheat chromosomes 2A and 2D. In situ hybridization using biotinylated genomic DNA of Ag. trichophorum cv. Greenleaf blocked with CS DNA failed to identify the alien chromosomes in 'Agrotana', indicating that the alien chromosomes were not likely derived from pubescent wheatgrass. In situ hybridization using labelled wheat genomic DNA blocked with 'Agrotana' DNA revealed that 'Agrotana' had 40 wheat, 14 alien, and 2 (a pair) wheat–alien translocated chromosomes. There was no homology between wheat and the alien chromosomes or chromosome segments involved in the wheat–alien recombinant. Two of the seven pairs of alien chromosomes were homoeologous to each other. The ability to identify alien chromatin in wheat using labelled wheat DNA instead of labelled alien DNA will be particularly useful in chromosome engineering of wheat germplasms having alien chromatin of unknown origin.Key words: wheat–alien hybrid, C-banding, fluorescence in situ hybridization, labelled wheat DNA as probe.

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