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

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.

1990 ◽  
Vol 17 (3) ◽  
pp. 239 ◽  
Author(s):  
LH Ji ◽  
P Langridge

Bread wheat is an allohexaploid with three pairs of homoeologous chromosomes. This means that each chromosome pair is present in three related but not truly homologous chromosomes. In order to maintain the integrity of the three chromosome sets, pairing must be very tightly controlled at meiosis to allow homologous but not homoeologous chromosomes to pair and recombine. Several genes (termed Ph genes) are known to be involved in controlling chromosome pairing in wheat, but the strongest effect has been associated with a gene on the long arm of chromosome 5B, Phl. The manipulation of this gene can be used to induce recombination between chromosomes that will not normally pair at meiosis. This has application in the introduction of new genetic information into wheat. Elucidation of the mechanism of action of the Ph genes has centred around genetic and cytogenetic studies with little attempt to investigate the molecular biology or biochemistry of these genes. Isolation of genes in meiosis in yeast and genes associated with the aerly stages of meiosis in lily have provided a potential entry point into the identification of the analogous genes in wheat.


1983 ◽  
Vol 25 (5) ◽  
pp. 487-494
Author(s):  
I. M. Rahn ◽  
A. Martinez

Chromosome pairing in females and males of diploid (2n = 22) and tetraploid (2n = 44) Odontophrynus americanus and diploid Ceratophrys cranwelli (2n = 26) and tetraploid C. ornata (2n = 104) showed that diploid females formed more chiasmata per paired arm than diploid males and polyploids of both sexes. There was a reduction in the level of recombination in female polyploids by forming multivalents with terminal chiasmata. The reduction reflected a change in the genetic control of pairing in females after polyploidization.


1970 ◽  
Vol 12 (1) ◽  
pp. 36-43 ◽  
Author(s):  
Hugh Thomas

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.


Genome ◽  
1991 ◽  
Vol 34 (6) ◽  
pp. 860-867 ◽  
Author(s):  
Kevin B. Jensen ◽  
Richard R.-C. Wang

Two accessions of Elymus caucasicus (Koch) Tzvelev and three accessions of Elymus longearistatus (Boiss.) Tzvelev were studied to determine the meiotic behavior and chromosome pairing in the two taxa, their interspecific hybrid, and their hybrids with various "analyzer" parents. Interspecific and intergeneric hybrids of the target taxa were obtained with the following analyzer species: Pseudoroegneria spicata (Pursh) A. Löve (2n = 14, SS), Pseudoroegneria libanotica (Hackel) D. R. Dewey (2n = 14, SS), Hordeum violaceum Boiss. &Hohenacker (2n = 14, HH) (= Critesion violaceum (Boiss. &Hohenacker) A. Löve), Elymus lanceolatus (Scribn. &Smith) Gould (2n = 28, SSHH), Elymus abolinii (Drob.) Tzvelev (2n = 28, SSYY), Elymus pendulinus (Nevski) Tzvelev (2n = 28, SSYY), Elymus fedtschenkoi Tzvelev (2n = 28, SSYY), Elymus panormitanus (Parl.) Tzvelev (2n = 28, SSYY), and Elymus drobovii (Nevski) Tzvelev (2n = 42, SSHHYY). Cytological analysis of their F1 hybrids showed that E. caucasicus and E. longearistatus were allotetraploids comprising the same basic genomes. Chromosome pairing in the E. caucasicus × P. libanotica hybrid demonstrated that the target taxa contained the S genome, based on 6.1 bivalents per cell. The lack of chromosome pairing, less than one bivalent per cell, in the E. longearistatus × H. violaceum hybrid showed that the H genome was absent. Increased pairing in the tetraploid and pentaploid hybrids when the Y genome was introduced indicated that the second genome in the two taxa was a segmental homolog of the Y genome. The S and Y genomes in E. caucasicus and E. longearistatus have diverged from each other and from those in many of the eastern and central Asian SY tetraploids.Key words: genome, meiosis, chromosome pairing, morphology, hybrid, Triticeae.


Genome ◽  
1988 ◽  
Vol 30 (1) ◽  
pp. 1-7 ◽  
Author(s):  
H. W. Rines ◽  
S. S. Johnson

Three meiotic synapsis-deficient mutants of oats (Avena sativa L.) were analyzed to determine their inheritance pattern, detailed chromosomal behavior, and location to chromosome. These highly sterile mutants, one in the cultivar 'Stout' and two in 'Noble', had been recovered from progeny of sodium azide mutagenized populations. Each segregated as a single gene recessive. The only synapsis-deficient variants previously described in hexaploid oats have been nullisomics or ditelosomics. Mutant 'Stout 1212' was classified as asynaptic due to deficiencies in chromosome pairing at all meiotic stages. Mutants 'Noble 1362' and 'Noble 1911' were classified as desynaptic since their homologous chromosomes were paired in early meiosis but they disassociated prematurely in late prophase I. Using a partial monosomic series from the Welsh Plant Breeding Station, mutant 1212 was mapped to monosome XII and is probably a mutation in Syn-5, a gene previously defined only by its nulli effect. Mutants 1362 and 1911 were mapped to monosome IV and are probably mutations in Syn-1, a gene also previously defined only by its nulli effect. Seed set on the synaptic mutant plants in the field was less than 0.2% of that on fertile sibs and likely resulted from pollination by surrounding fertile plants. This seed may serve as a source of unique aneuploid stocks in oats.Key words: meiotic mutants, gene mapping, monosomics, nullisomics, oat cytogenetics.


1970 ◽  
Vol 12 (4) ◽  
pp. 876-881 ◽  
Author(s):  
J. P. Dubuc ◽  
R. C. McGinnis

A ditelosomic line was crossed with 12 identified monosomics. The metaphase I pairing was studied in the 40 + t – chromosome progenies. The telocentric chromosome was found to be homologous to the three previously identified monosomics namely, −7, −10, and −20 suggesting that the same chromosome is missing in all three lines. None of the chromosomes in monosomic condition used in the crosses except ST-7 and ST-17 from A. byzantina were involved in the reciprocal translocation present between Sun II and Garry and Rodney.The gene for normal vs. abaxial curling of the leaves was located on the short arm of chromosome 20. The genes for diploidisation and normal vs. kinky neck were located on 20L.


1982 ◽  
Vol 24 (4) ◽  
pp. 397-408 ◽  
Author(s):  
U. Kushnir ◽  
G. M. Halloran

Two mutants, each promoting homoeologous chromosome pairing in hexaploid wheat (Triticum × aestivum L. emend gr. aestivum), in the cultivar Chinese Spring, ph1b at the Ph locus on chromosome 5BL and the other, ph2, on chromosome 3DS, were compared for their influence on chromosome pairing and fertility in pentaploid hybrids with Triticum turgidum L. emend var. dicoccoides (Korn. in litt. in Schweinf.). The mutants induced increased multivalent frequency over the normal pentaploid. Lower univalent frequencies in the ph2-pentaploid, compared with the normal pentaploid, indicated that D-genome chromosomes of the former were substantially involved in homoeologous pairing. Certain differences in other meiotic processes and fertility among the pentaploids may reflect differences in the activity of the pairing genes. There appeared to be a higher level of univalent elimination in pollen and egg cells in the ph2-, compared with the ph1b-pentaploid. Tetrad formation was close to normal in the ph2- pentaploid but exhibited high levels of abnormality (monads, dyads, triads and apolar tetrads) in the ph1b-pentaploid. Fertility levels in crosses of the pentaploids with hexaploid wheat, while low, were much lower for the ph1b-, compared with the ph2-pentaploid.


1984 ◽  
Vol 26 (3) ◽  
pp. 264-271 ◽  
Author(s):  
Kunio Kitada ◽  
Takeshi Omura

One complete asynaptic mutant, MM-19, and two partial ones, MM-4 and MM-16, of Oryza sativa L. induced by N-methyl-N-nitrosourea (MNU) were cytogenetically investigated. No chromosome pairing occurred from zygotene to pachytene and 24 univalents appeared at diakinesis and metaphase 1 in MM-19. On the other hand, a partial lack of chromosome pairing was observed from zygotene to pachytene and various numbers of univalents occurred at metaphase I in MM-4 and MM-16. The mean chiasma frequency per bivalent as well as per cell decreased to different extents in MM-4 and MM-16, and the correlation between both the amount of chromosome pairing from zygotene to pachytene and the chiasma frequency per cell at diakinesis was recognized. Judging from the development of anthers in each meiotic stage, the duration of the stage forming the synizetic knot, at which chromosome pairing took place, was longer in MM-4 and MM-16 than in the normal plant, and was in MM-19 almost as long as in the normal plant. The results of gene analyses indicate that each of the three asynaptic mutants is controlled by a recessive gene and that, at least for MM-4 and MM-16, these genes are located at different loci.Key words: asynaptic, rice, Oryza, chiasma frequency, synizesis.


1971 ◽  
Vol 18 (3) ◽  
pp. 311-328 ◽  
Author(s):  
A. M. Wall ◽  
Ralph Riley ◽  
Victor Chapman

SUMMARYPlants of Triticum aestivum (2n = 6x = 42) ditelocentric 5BL were treated with EMS in order to produce mutations in the 5B system by which meiotic pairing between homoeologous chromosomes is normally prevented. To check for the occurrence of mutation T. aestivum ditelo-5BL plants were pollinated with rye (Secale cereale 2n = 14) and meiosis was examined in the resulting hybrids.Wheat-rye hybrids were scored for the presence of mutants when the wheat parents were either the EMS-treated wheat plants, or their selfed derivatives, or their progenies obtained after pollination with untreated euploid individuals.Mutants were detected by each of these procedures and mutant gametes were produced by the treated ditelocentric plants with frequencies between 1·5 and 2·5%, but there were differences between the mutants in the extent to which homoeologous pairing occurred in the derived wheat-rye hybrids. The differences may have resulted from the occurrence of mutation at different loci or to different extents at the same locus.Two mutants, Mutant 10/13 and Mutant 61, were fixed in the homozygous condition. Mutant 10/13 was made homozygous both in the 5BL ditelocentric and in the euploid conditions but these genotypes regularly formed 21 bivalents at meiosis, and there was no indication of homoeologous pairing although the mutant 10/13 gave rise to homoeologous pairing in wheat-rye hybrids.


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