The genomic relationship of the diploid Bromus variegatus to Bromus inermis

1984 ◽  
Vol 26 (4) ◽  
pp. 469-474 ◽  
Author(s):  
K. C. Armstrong
Keyword(s):  
Chromosome Pairing ◽  
Diploid Species ◽  
Bromus Inermis ◽  
Genomic Relationship ◽  
Diploid Genome ◽  
B Genome ◽  
Hybrid Plants ◽  
Relationship Of ◽  
Genomic Model

The diploid species Bromus variegatus Bieb. was crossed to Bromus inermis Leyss (4x, 8x). Chromosome pairing in each of the six F1 hybrid plants of B. variegatus × B. inermis (4x) fit a 2:1 genomic model of chromosome pairing, which indicated that the B. variegatus genome was more closely related to the A or B genome of B. inermis than A and B were related to each other. A breakdown of microsporocytes was observed in the B. variegatus × B. inermis (8x) hybrid. However, chromosome pairing suggested that the B. variegatus genome was differentiated from the A and B genomes of octoploid B. inermis.Key words: Bromus, diploid, genome, affinity.

Dilemma of genome relationship in the diploid species Thinopyrum bessarabicum and Thinopyrum elongatum (Triticeae: Poaceae)

Genome ◽  
1990 ◽  
Vol 33 (6) ◽  
pp. 944-946 ◽  
Author(s):  
Prem P. Jauhar
Keyword(s):  
Chromosome Pairing ◽  
Constitutive Heterochromatin ◽  
Diploid Species ◽  
Total Content ◽  
Ploidy Levels ◽  
5S Dna ◽  
Thinopyrum Bessarabicum ◽  
Thinopyrum Elongatum ◽  
Relationship Of ◽  
The Relationship

Evidence on the relationship of the J genome of diploid Thinopyrum bessarabicum and the E genome of diploid Thinopyrum elongatum (= Lophopyrum elongatum) is discussed. Low chromosome pairing between J and E at different ploidy levels, suppression of J–E pairing by the Ph1 pairing regulator that inhibits homoeologous pairing, complete sterility of the diploid hybrids (JE), karyotypic differentiation of the two genomes and differences in their biochemical organization as reflected in total content and distribution of constitutive heterochromatin, and marked differences in isozymes, 5S DNA, and rDNA indicate that J and E are distinct genomes. These genomes are homoeologous and not homologous. There is no justification for the merger of J and E genomes.Key words: chromosome pairing, Ph1 pairing regulator, C-banding, isozymes, 5S DNA, rDNA.

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.

HYBRIDS BETWEEN A DIPLOID AGROPYRON ELONGATUM AND AEGILOPS SQUARROSA

1971 ◽  
Vol 13 (1) ◽  
pp. 90-94 ◽  
Author(s):  
J. Dvořák
Keyword(s):  
Chromosome Pairing ◽  
Agropyron Elongatum ◽  
B Genome ◽  
Hybrid Plants ◽  
Aegilops Squarrosa ◽  
High Degree

Hybrids were obtained in crosses between Aegilops squarrosa and Agropyron elongatum (2x) but not in crosses between Ag. elongatum and Ae. speltoides and T. boeoticum, respectively. Chromosome pairing revealed a rather high degree of homoeology between the genomes of Ae. squarrosa and Ag. elongatum. The average pairing was 10.7′ + 1.5″ + 0.027″′ per cell with a range of from 0 to 5 pairs. All F1 hybrid plants were sterile with very low pollen fertility.It is proposed that the A and D genomes of wheat are more closely related to the genomes of section Elytrigia of the genus Agropyron than is the B genome.

scholarly journals LATENT NONSTRUCTURAL DIFFERENTIATION AMONG HOMOLOGOUS CHROMOSOMES AT THE DIPLOID LEVEL: CHROMOSOME 6Be OF AEGILOPS LONGISSIMA

Genetics ◽  
1986 ◽  
Vol 114 (2) ◽  
pp. 579-592
Author(s):  
Rama S Kota ◽  
Patrick E McGuire ◽  
Jan Dvořák
Keyword(s):  
Chromosome Pairing ◽  
Chinese Spring ◽  
Constitutive Heterochromatin ◽  
Diploid Species ◽  
Triticum Aestivum L ◽  
Homologous Chromosomes ◽  
B Genome ◽  
Aegilops Longissima ◽  
Chinese Spring Wheat ◽  
Diploid Level

ABSTRACT Previous work has shown that chromosome pairing at metaphase I (MI) of wheat homologous chromosomes from different inbred lines (heterohomologous chromosomes) is reduced relative to that between homologous chromosomes within an inbred line (euhomologous chromosomes). In order to determine if a potential for this phenomenon exists in diploid species closely related to the wheat B genome, MI chromosome pairing was investigated between euhomologous and heterohomologous 6Be (=6Se) chromosomes, each from a different population of Aegilops longissima Schweinf. et Muschl. (2n = 2x = 14) substituted for chromosome 6B of Chinese Spring wheat (Triticum aestivum L., 2n = 6x = 42). Euhomologous and heterohomologous monotelodisomics, i.e., plants with one complete chromosome 6Be and a telosome of either 6Bep or 6Beq, were constructed in the isogenic background of Chinese Spring. Pairing at MI of the Ae. longissima chromosomes was reduced in heterohomologous monotelodisomics compared to that in the corresponding euhomologous monotelodisomics. The remaining 20 pairs of Chinese Spring chromosomes paired equally well in the euhomologous and heterohomologous monotelodisomics. Thus, the cause of the reduced pairing must reside specifically in the Ae. longissima heterohomologues. In the hybrids between the Ae. longissima lines that contributed the substituted chromosomes, pairing between the heterohomologous chromosomes was normal and did not differ from that of the euhomologous chromosomes. These data provide evidence that a potential for reduced pairing between the heterohomologues is present in the diploid species, but is expressed only in the polyploid wheat genetic background. The reduction in heterohomologous chromosome pairing was greater in the p arm than in the q arm, exactly as in chromosome 6B of wheat. It is concluded that the reduced pairing between Ae. longissima heterohomologues has little to do with constitutive heterochromatin. The value of chromosome pairing as an unequivocal means of determining the origin of genomes in polyploid plants is questioned.

GENOME RELATIONS BETWEEN PASPALUM CONSPERSUM AND TWO DIPLOID PASPALUM SPECIES

1978 ◽  
Vol 20 (3) ◽  
pp. 365-372 ◽  
Author(s):  
Byron L. Burson
Keyword(s):  
Chromosome Number ◽  
Chromosome Pairing ◽  
Mean Frequency ◽  
Hybrid Plants ◽  
The Mean ◽  
The Cross ◽  
Relationship Of ◽  
The Relationship

Paspalum conspersum Schrad. ex Schult., 2n = 4x = 40, was crossed with P. intermedium Munro ex Morong, 2n = 2x = 20, and P. jurgensii Hackel, 2n = 2x = 20, and the hybrids were studied cytologically to determine the relationship between these species. Thirteen P. intermedium × P. conspersum hybrid plants were produced; however, only eight survived. They had a chromosome number of 2n = 3x = 30. Meiosis was irregular with a chromosome pairing relationship of 19.87 univalents, 5.03 bivalents, and 0.03 trivalents per cell. These findings suggested that the two species have a partially homologous genome. The two hybrids obtained from the cross between P. jurgensii and P. conspersum had a chromosome number of 2n = 3x = 30. The mean chromosome pairing in these hybrids was 10.12 univalents. 9.86 bivalents, 0.08 trivalents, and 0.004 quadrivalents. The close bivalent pairing and a mean frequency of 9.86 bivalents suggested that the P. jurgensii genome was homologous to one genome of P. conspersum. Limited autosyndetic pairing of the P. conspersum chromosomes was also detected in both groups of hybrids. A standardization of genome formulas for the genus was proposed in which P. intermedium, P. jurgensii, and P. conspersum were represented by genome formulas of II, JJ, and I2I2 JJ, respectively. The genome relationships and formulas were discussed for other related Paspalum species.

Cytogenetic relationship within cultivated Brassica analyzed in amphihaploids from the three diploid ancestors

1986 ◽  
Vol 28 (3) ◽  
pp. 323-329 ◽  
Author(s):  
T. Attia ◽  
G. Röbbelen
Keyword(s):  
Chromosome Pairing ◽  
Common Ancestor ◽  
Diploid Species ◽  
Ancestral Genome ◽  
Homologous Pairing ◽  
B Genome ◽  
Close Relationship ◽  
Chromosomal Interchange ◽  
Low Degrees ◽  
High Level

To investigate the factors controlling evolutionary differentiation within the genus Brassica, chromosome pairing in amphihaploids from crosses between the three elementary diploid species B. campestris (AA), B. oleracea (CC), and B. nigra (BB) was analyzed. The amphihaploid AC showed a high amount of pairing, while the two amphihaploids AB and BC, both including the genome of B. nigra, exhibited only low degrees of chromosome association. By the occurrence of tetra- and penta-valents, auto- as well as allo-syndetic pairing was demonstrated to exist in the AC amphihaploid. True homologous pairing between the genomes A and C was deduced from the occurrence of chromosomal interchange configurations. Although the genomes of B. oleracea and B. campestris are evolutionarily distinct, as shown by the different number and structure of their chromosomes, their close relationship is readily evident from the high level of pairing observed in the AC amphihaploids. On the other hand, the much lower pairing within the amphihaploids including the B genome is unexpected in view of the hypothesis of a common ancestor for all three of the cultivated Brassica diploids from an ancestral genome with x = 6 chromosomes. It is discussed whether B. nigra is indeed more distantly related to the two other species or whether this genome carries a suppressor of chromosome pairing.Key words: chromosome pairing, amphihaploids, evolutionary relations.

CHROMOSOME RELATIONSHIPS BETWEEN THE CULTIVATED OAT AVENA SATIVA (6x) AND A. VENTRICOSA (2x)

1970 ◽  
Vol 12 (1) ◽  
pp. 36-43 ◽  
Author(s):  
Hugh Thomas
Keyword(s):  
Chromosome Pairing ◽  
Avena Sativa ◽  
Diploid Species ◽  
Meiotic Behaviour ◽  
Hexaploid Species ◽  
C Genome

Chromosome pairing in the F1 hybrid between the cultivated oat Avena sativa and a diploid species A. ventricosa, and in the derived amphiploid, shows that the diploid species is related to one of the genomes of the hexaploid species. The amount of chromosome pairing observed in complex interamphiploid hybrids demonstrates further that A. ventricosa is related to the C. genome of A. sativa. However, the chromosomes of the diploid species have become differentiated from that of the C genome of A. sativa and this is readily apparent in the meiotic behaviour of both the F1 hybrid and the amphiploid.

A Centromeric Tandem Repeat Family Originating From a Part of Ty3/gypsy-Retroelement in Wheat and Its Relatives

Genetics ◽  
2003 ◽  
Vol 164 (2) ◽  
pp. 665-672 ◽  
Author(s):  
Zhi-Jun Cheng ◽  
Minoru Murata
Keyword(s):  
In Situ Hybridization ◽  
Tandem Repeats ◽  
Diploid Species ◽  
Upstream Region ◽  
Aegilops Speltoides ◽  
Repeat Family ◽  
B Genome ◽  
Intervening Sequences ◽  
Wild Diploid Species

AbstractFrom a wild diploid species that is a relative of wheat, Aegilops speltoides, a 301-bp repeat containing 16 copies of a CAA microsatellite was isolated. Southern blot and fluorescence in situ hybridization revealed that ∼250 bp of the sequence is tandemly arrayed at the centromere regions of A- and B-genome chromosomes of common wheat and rye chromosomes. Although the DNA sequence of this 250-bp repeat showed no notable homology in the databases, the flanking or intervening sequences between the repeats showed high homologies (>82%) to two separate sequences of the gag gene and its upstream region in cereba, a Ty3/gypsy-like retroelement of Hordeum vulgare. Since the amino acid sequence deduced from the 250 bp with seven CAAs showed some similarity (∼53%) to that of the gag gene, we concluded that the 250-bp repeats had also originated from the cereba-like retroelements in diploid wheat such as Ae. speltoides and had formed tandem arrays, whereas the 300-bp repeats were dispersed as a part of cereba-like retroelements. This suggests that some tandem repeats localized at the centromeric regions of cereals and other plant species originated from parts of retrotransposons.

Suppression of homologous pairing between chromosomes of A and B genomes of 4x and 6x wheats by Hordeum californicum Covas and Stebbins

Genome ◽  
1988 ◽  
Vol 30 (1) ◽  
pp. 8-11
Author(s):  
H. S. Balyan ◽  
G. Fedak
Keyword(s):  
Chromosome Pairing ◽  
Chinese Spring ◽  
Chiasma Frequency ◽  
Mother Cell ◽  
Triticum Turgidum ◽  
Regulatory Gene ◽  
Intergeneric Hybrids ◽  
Homologous Pairing ◽  
Meiotic Analysis ◽  
Hybrid Plants

Three hybrids of Triticum turgidum cv. Ma with Hordeum californicum × T. aestivum cv. Chinese Spring amphiploid were obtained at a frequency of 1.6% of the pollinated florets. Meiotic analysis of the hybrid plants revealed an average chiasma frequency per pollen mother cell ranging from 15.27 to 17.60. The lower than expected chromosome pairing in the hybrid plants was attributed to the suppression of pairing between homologous wheat chromosomes by pairing regulatory gene(s) in H. californicum.Key words: intergeneric hybrids, Hordeum californicum, Triticum turgidum, meiosis, chromosome pairing.

Evidence for genetic suppression of heterogenetic chromosome pairing in polyploidy species of Solanum, sect. Petota

1983 ◽  
Vol 25 (5) ◽  
pp. 530-539 ◽  
Author(s):  
Jan Dvořák
Keyword(s):  
Chromosome Pairing ◽  
Interspecific Hybrids ◽  
Diploid Species ◽  
Diploid Hybrid ◽  
Polyploid Species ◽  
Chromosome Differentiation ◽  
Genetic Suppression ◽  
Solanum Sect ◽  
Paradoxical Results

Data on chromosome pairing in haploids and interspecific hybrids of Solanum, sect. Petota reported in the literature were used to determine whether the diploidlike chromosome pairing that occurs in some of the polyploid species of the section is regulated by the genotype or brought about by some other mechanism. The following trends emerged from these data. Most of the polyploid × polyploid hybrids had high numbers of univalents, which seemed to indicate that the polyploid species were constructed from diverse genomes. Haploids, except for those derived from S. tuberosum, had incomplete chromosome pairing. All hybrids from diploid × diploid crosses had more or less regular chromosome pairing, which suggested that all investigated diploid species have the same genome. Likewise, hybrids from polyploid × diploid crosses had high levels of chromosome pairing. These paradoxical results are best explained if it is assumed that (i) the genotypes of most polyploid species, but not those of the diploid species, suppress heterogenetic pairing, (ii) that nonstructural chromosome differentiation is present among the genomes of both diploid and polyploid species, and (iii) the presence of the genome of a diploid species in a polyploid × diploid hybrid results in promotion of heterogenetic pairing. It is, therefore, concluded that heterogenetic pairing in most of the polyploid species is genetically suppressed.

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