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.

CHROMOSOME RELATIONSHIPS BETWEEN AVENA SATIVA AND THE TWO DIPLOID SPECIES A. CANARIENSIS AND A. PROSTRATA

1974 ◽  
Vol 16 (4) ◽  
pp. 889-894 ◽  
Author(s):  
Hugh Thomas ◽  
J. M. Leggett
Keyword(s):  
Chromosome Pairing ◽  
Avena Sativa ◽  
Diploid Species ◽  
Morphological Features ◽  
Tetraploid Hybrid ◽  
Hexaploid Species

Although the diploid species Avena canariensis has a number of morphological features in common with the hexaploid species of Avena, the degree of chromosome pairing in the tetraploid hybrid A. canariensis × A. sativa did not reveal closer homology with A. sativa than that of another diploid species, A. prostrata. The chromosomes of both these newly described diploid species are only partially homologous with one of the genomes of A. sativa. The two diploid species A. prostrata and A. canariensis are differentiated by translocations involving three pairs of chromosomes.

The genomic identification of some monosomics of Avena sativa L. cv. Sun II using genomic in situ hybridization

Genome ◽  
1995 ◽  
Vol 38 (4) ◽  
pp. 747-751 ◽  
Author(s):  
J. M. Leggett ◽  
G. S. Markhand
Keyword(s):  
In Situ Hybridization ◽  
Avena Sativa ◽  
Genomic Dna ◽  
Diploid Species ◽  
Genomic In Situ Hybridization ◽  
Chromosome Translocations ◽  
C Genome

Genomic in situ hybridization using total genomic DNA extracted from the C genome diploid species Avena eriantha (2n = 2x = 14, genome CpCp) was used to identify monosomics (2n = 6x − 1 = 41) of the constituent genomes of the hexaploid cultivated oat A. sativa L. cv. Sun II (2n = 6x = 42, genomes AACCDD). The results demonstrate 3 AD/C and 6 C/AD chromosome translocations, indicate that five of the missing monosomics are derived from the C genome, and show that there are duplicates within the partial monosomic series. Chromosome polymorphisms between some monosomic lines are also demonstrated.Key words: Avena, monosomics, genomic in situ hybridization, genomic identification.

Molecular diversity of the 5S rRNA gene and genomic relationships in the genus Avena (Poaceae: Aveneae)

Genome ◽  
2008 ◽  
Vol 51 (2) ◽  
pp. 137-154 ◽  
Author(s):  
Yuan-Ying Peng ◽  
Yu-Ming Wei ◽  
Bernard R. Baum ◽  
You-Liang Zheng
Keyword(s):  
Molecular Diversity ◽  
Diploid Species ◽  
5S Rdna ◽  
Rrna Gene ◽  
D Genome ◽  
Rdna Sequences ◽  
Unit Classes ◽  
Hexaploid Species ◽  
Unit Class ◽  
C Genome

The molecular diversity of the rDNA sequences (5S rDNA units) in 71 accessions from 26 taxa of Avena was evaluated. The analyses, based on 553 sequenced clones, indicated that there were 6 unit classes, named according to the haplomes (genomes) they putatively represent, namely the long A1, long B1, long M1, short C1, short D1, and short M1 unit classes. The long and short M1 unit classes were found in the tetraploid A. macrostachya , the only perennial species. The long M1 unit class was closely related to the short C1 unit class, while the short M1 unit class was closely related to the long A1 and long B1 unit classes. However, the short D1 unit class was more divergent from the other unit classes. There was only one unit class per haplome in Avena, whereas haplomes in the Triticeae often have two. Most of the sequences captured belonged to the long A1 unit class. Sequences identified as the long B1 unit class were found in the tetraploids A. abyssinica and A. vaviloviana and the diploids A. atlantica and A. longiglumis . The short C1 unit class was found in the diploid species carrying the C genome, i.e., A. clauda, A. eriantha , and A. ventricosa , and also in the diploid A. longiglumis, the tetraploids A. insularis and A. maroccana , and all the hexaploid species. The short D1 unit class was found in all the hexaploid species and two clones of A. clauda. It is noteworthy that in previous studies the B genome was found only in tetraploid species and the D genome only in hexaploid species. Unexpectedly, we found that various diploid Avena species contained the B1 and D1 units. The long B1 unit class was found in 3 accessions of the diploid A. atlantica (CN25849, CN25864, and CN25887) collected in Morocco and in 2 accessions of A. longiglumis (CIav9087 and CIav9089) collected in Algeria and Libya, respectively, whereas only 1 clone of A. clauda (CN21378) had the short D1 unit. Thus there might be a clue as to where to search for diploids carrying the B and D genomes. Avena longiglumis was found to be the most diverse species, possibly harboring the A, B, and C haplomes. The long M1 and short M1 are the unit classes typical of A. macrostachya. These results could explain the roles of A. clauda, A. longiglumis, and A. atlantica in the evolution of the genus Avena. Furthermore, one clone of the tetraploid A. murphyi was found to have sequences belonging to the short D1 unit class, which could indicate that A. murphyi might have been the progenitor of hexaploid oats and not, as postulated earlier, A. insularis. The evolution of Avena did not follow the molecular clock. The path inferred is that the C genome is more ancient than the A and B genomes and closer to the genome of A. macrostachya, the only existing perennial, which is presumed to be the most ancestral species in the genus.

Assessment of chromosome associations in haploids and their parental accessions in Hordeum

Genome ◽  
1988 ◽  
Vol 30 (2) ◽  
pp. 204-210 ◽  
Author(s):  
R. von Bothmer ◽  
N. C. Subrahmanyam
Keyword(s):  
Genetic Variation ◽  
Chromosome Pairing ◽  
Diploid Species ◽  
Meiotic Behaviour ◽  
Meiotic Pairing ◽  
Homoeologous Pairing ◽  
Homoeologous Chromosome ◽  
Homologous Pairing ◽  
Homoeologous Chromosome Pairing ◽  
Chromosome Associations

Meiotic pairing was studied in the following species and their haploid derivatives: Hordeum cordobense 2x, H. marinum 2x and 4x, H. secalinum 4x, H. capense 4x, H. jubatum 4x, H. brachyantherum 4x and 6x, H. lechleri 6x, and H. procerum 6x. The study revealed (i) homologous pairing in diploid species and very little nonhomologous associations in their mono-haploids; (ii) the alloploid nature of the polyploid taxa; (iii) a certain degree of homoeologous pairing in polyhaploids despite the diploid-like meiotic behaviour of the polyploids; (iv) genetic variation in the suppression of homoeologous chromosome pairing in different Hordeum species.Key words: Hordeum, meiotic pairing, haploids.

Cytoplasmic substitutions involving six Avena species

1984 ◽  
Vol 26 (6) ◽  
pp. 698-700 ◽  
Author(s):  
J. M. Leggett
Keyword(s):  
Growth Rate ◽  
Avena Sativa ◽  
Diploid Species ◽  
Quantitative Inheritance ◽  
Alloplasmic Lines ◽  
Avena Species ◽  
Flowering Date ◽  
Cytoplasmic Effects ◽  
C Genome ◽  
Nuclear Genomes

Alloplasmic lines involving the nuclear genomes of the hexaploid oat Avena sativa, the cytoplasms of the diploid species A. canariensis, A. hirtula, A. pilosa, A. prostrata, and A. ventricosa, and the tetraploid A. barbata have been produced. The cytoplasmic effects on growth rate and flowering date are described with particular reference to the introduction of the cytoplasm from the two C-genome diploid species.Key words: Avena, quantitative inheritance, cytoplasmic effects.

EVOLUTION OF AVENA SATIVA: ORIGIN OF THE CYTOPLASMIC GENOME

1976 ◽  
Vol 18 (4) ◽  
pp. 769-771 ◽  
Author(s):  
Martin W. Steer ◽  
Hugh Thomas
Keyword(s):  
Avena Sativa ◽  
Conclusive Evidence ◽  
Cytoplasmic Genome ◽  
A Genome ◽  
Isoelectric Points ◽  
C Genome

Comparisons of the isoelectric points of the large subunits from the enzyme ribulose biphosphate carboxylase, extracted from species and hybrids of Avena, provide conclusive evidence for the origin of the cytoplasmic genome of the hexapioid A. sativa L. from the A. genome diploids rather than the C genome diploids.

THE MEIOTIC BEHAVIOR OF ANEUPOLYHAPLOIDS OF THE CULTIVATED OAT AVENA SATIVA (2n = 6x = 42)

1977 ◽  
Vol 19 (4) ◽  
pp. 651-656 ◽  
Author(s):  
J. M. Leggett
Keyword(s):  
Genetic Control ◽  
Chromosome Pairing ◽  
Avena Sativa ◽  
Meiotic Behavior ◽  
Homoeologous Chromosomes

Chromosome pairing and the frequency of secondary associations in two aneupolyhaploid plants of A. sativa are described. There was little evidence of pairing between homoeologous chromosomes in either plant. The results are discussed in relation to the genetic control of bivalent pairing in A. sativa and the possible divergence between the constituent genomes.

The use of double fluorescence in situ hybridization to physically map the positions of 5S rDNA genes in relation to the chromosomal location of 18S–5.8S–26S rDNA and a C genome specific DNA sequence in the genus Avena

Genome ◽  
1996 ◽  
Vol 39 (3) ◽  
pp. 535-542 ◽  
Author(s):  
Concha Linares ◽  
Juan González ◽  
Esther Ferrer ◽  
Araceli Fominaya
Keyword(s):  
In Situ Hybridization ◽  
Dna Sequence ◽  
Diploid Species ◽  
5S Rdna ◽  
Rdna Genes ◽  
26S Rdna ◽  
A Genome ◽  
Rdna Loci ◽  
C Genome

A physical map of the locations of the 5S rDNA genes and their relative positions with respect to 18S–5.8S–26S rDNA genes and a C genome specific repetitive DNA sequence was produced for the chromosomes of diploid, tetraploid, and hexaploid oat species using in situ hybridization. The A genome diploid species showed two pairs of rDNA loci and two pairs of 5S loci located on both arms of one pair of satellited chromosomes. The C genome diploid species showed two major pairs and one minor pair of rDNA loci. One pair of subtelocentric chromosomes carried rDNA and 5S loci physically separated on the long arm. The tetraploid species (AACC genomes) arising from these diploid ancestors showed two pairs of rDNA loci and three pairs of 5S loci. Two pairs of rDNA loci and 2 pairs of 5S loci were arranged as in the A genome diploid species. The third pair of 5S loci was located on one pair of A–C translocated chromosomes using simultaneous in situ hybridization with 5S rDNA genes and a C genome specific repetitive DNA sequence. The hexaploid species (AACCDD genomes) showed three pairs of rDNA loci and six pairs of 5S loci. One pair of 5S loci was located on each of two pairs of C–A/D translocated chromosomes. Comparative studies of the physical arrangement of rDNA and 5S loci in polyploid oats and the putative A and C genome progenitor species suggests that A genome diploid species could be the donor of both A and D genomes of polyploid oats. Key words : oats, 5S rDNA genes, 18S–5.8S–26S rDNA genes, C genome specific repetitive DNA sequence, in situ hybridization, genome evolution.

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.

Meiotic behaviour of induced autotetraploids in Triticum L.

Genome ◽  
1990 ◽  
Vol 33 (2) ◽  
pp. 302-307 ◽  
Author(s):  
Yang Yen ◽  
Gordon Kimber
Keyword(s):  
Chromosome Pairing ◽  
Seed Set ◽  
Chromosome Association ◽  
Meiotic Behaviour ◽  
Meiotic Analysis

Colchicine-induced autotetraploids of Triticum speltoides, T. longissimum, T. sharonense, T. bicorne, T. uniaristatum, T. monococcum, and T. tauschii were all morphologically similar to but larger than their diploid forms. Seed set was lower than in the diploids except for the autotetraploid T. speltoides. Meiotic analysis showed fewer quadrivalents and more bivalents than would be expected in all of these autotetraploids. Arm-pair switch, indicated by complex trivalents and quadrivalents, was found and involved 0.1% of total chromosomes in T. umbellulatum, 0.5% in T. longissimum, 0.7% in both T. sharonense and T. tauschii, 6.3% in T. bicorne, and 15.3% in T. uniaristatum.Key words: meiosis, chromosome association, arm-pair switch, chromosome pairing, bivalentization.

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