Meiotic pairing in haploids and amphidiploids of spontaneous versus synthetic origin in rape, Brassica napus L.

1986 ◽  
Vol 28 (3) ◽  
pp. 330-334 ◽  
Author(s):  
T. Attia ◽  
G. Röbbelen

Newly resynthesized AC amphihaploids, which were characterized by high meiotic pairing and multivalent formulation, after doubling of their chromosome number showed preferential pairing and bivalent formation in the resynthesized amphidiploid Brassica napus (AACC). However, univalents as well as multivalents were also formed indicating that their chromosome behaviour was not fully diploidized. Stabilization of chromosome pairing in newly resynthesized amphidiploids can be achieved through genetic control or structural modification of the homoeologous chromosomes. A comparison of the meiotic behaviour of spontaneous haploids of natural rapeseed with that of the newly synthesized AC amphihaploids provides some evidence that both processes may be involved in the regulation of chromosome pairing in Brassica.Key words: Brassica, amphihaploid, amphidiploid, meiosis, univalents, multivalents.

Genome ◽  
1988 ◽  
Vol 30 (3) ◽  
pp. 450-457 ◽  
Author(s):  
William Tai ◽  
H. Ikonen

Twenty five polyhaploid plants (2n = 2x = 19, genome formula AC) of Brassica napus (2n = 4x = 38, AACC) were cytogenetically studied. Seven of these were found among field populations and the rest were derived through anther culture of B. napus cv. Regent. Meiotic behaviour at diakinesis and metaphase I revealed nine bivalents and one univalent in more than 40% of the more than 400 pollen mother cells analyzed. However, when the chromosome number of the polyhaploids was doubled using colchicine, 19 bivalents were observed. These doubled plants (2n = 4x = 38, AACC) also had normal behaviour identical to a regular B. napus at other meiotic stages. Quadrivalent associations were observed when the chromosome numbers were doubled to the octaploid level (2n = 8x = 72, AAAACCCC). It is suggested that A and C are homoeologous genomes. If homologous partners are present, chromosomes would pair within the same genome to form bivalents as occurred in the allotetraploids and to form quadrivalents as occurred in the allooctaploids. However, when a homologous partner is not available, the homoeologous chromosomes would then pair to form bivalents in those polyhaploids.Key words: Brassica napus, polyhaploids, genome relationship, meiotic behaviour, homoeologous pairing.


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.


1971 ◽  
Vol 18 (3) ◽  
pp. 329-339 ◽  
Author(s):  
A. M. Wall ◽  
Ralph Riley ◽  
M. D. Gale

SUMMARYAn investigation was made of the chromosomal position of the mutant locus, in Mutant 10/13 of Triticum aestivum (2n = 6x = 42), affecting homoeologous chromosome pairing at meiosis. In hybrids between Mutant 10/13 and rye (Secale cereale 2n = 14), homoeologous chromosomes frequently pair at meiosis although normally, in wheat-rye hybrids, this happens infrequently.The association of the mutant condition with chromosome 5B was determined by (i) the absence of segregation in hybrids obtained when Mutant 10/13 monosomic 5B was pollinated by rye; (ii) the occurrence of trisomie segregation for pairing behaviour in 28-chromosome wheat-rye hybrids, obtained from SB trisomie wheat parents with two 5B chromosome from a non-mutant and one from a mutant parent; (iii) the absence of segregation for pairing behaviour in the 29-chromosome wheat-rye hybrids obtained from the same trisomie wheat parents.The alternative pairing behaviours segregated independently of the centromere when wheat plants that were simultaneously heteromorphic, 5BL telocentric/5B complete, and heterozygous for the Mutant 10/13 state, were pollinated by rye. The alternative chromosome-pairing patterns segregated to give a ratio not different from 1:1, so that the association of homoeologous pairing with Mutant 10/13 probably derived from the occurrence of mutation at a single locus on 5BL. In the disomic heteromorphic state, 5BL was 91 map units in length.Trisomie wheats with two complete 5B chromosomes and one 5BL telocentric, that were also heterozygous for the Mutant 10/13 condition, were pollinated by rye. Among the resulting 28-chromosome hybrids there was a 2:1 segregation of hybrids with low pairing: high (homoeologous) pairing and also of hybrids with complete 5B: telocentric 5BL. However, there was no evidence of linkage in this trisomie segregation. All the 29-chromosome hybrids from this cross had low pairing and it could be concluded that the single mutant allele, in Mutant 10/13, was recessive. In the trisomie condition, relative to a simplex situation, 5BL was 33·05 map units in length.The critical locus on 5BL was designated Pairing homoeologous. The normal dominant allele was symbolized Ph and the recessive allele, in Mutant 10/13, ph.The prevention of homoeologous pairing by the activity of a single locus makes the evolution of the regular meiotic behaviour of T. aestivum more readily comprehensible.


1984 ◽  
Vol 26 (6) ◽  
pp. 752-761 ◽  
Author(s):  
C. A. Newell ◽  
M. L. Rhoads ◽  
D. L. Bidney

Plants were regenerated from seedling tissue explants of four lines of winter rape (Brassica napus L.) including a cytoplasmic male sterile line carrying Raphanus sativus L. cytoplasm, and from leaf mesophyll protoplasts of the cytoplasmic male sterile line. Chromosome number variability was investigated in 102 regenerated plants. Mitotic root-tip cells were scored initially; those plants exhibiting mixoploidy or an altered chromosome number were reexamined at meiosis to confirm the presence of alterations in germ line cells. Plants regenerated from seedling explants included 2n = 38 diploids (87.0%) similar to the parental line, monosomics (7.8%), trisomics (2.6%), and 2n = 76 tetraploids (1.3%). The germ line number was not resolved in one mixoploid (1.3%). Protoplast-derived regenerated plants were diploid (44%), hypodiploid (20%), and tetraploid or hypotetraploid (36%). Meiotic analysis of regenerated plants showed a range of multiple chromosome associations with no plants consistently exhibiting bivalent formation only. Chromosomal alterations other than number may have been induced by culture, but could not be substantiated since multiple chromosome associations were also frequent in control plants grown from seed.Key words: plant regeneration, protoplast regeneration, Brassica napus, cytogenetics.


Genome ◽  
1988 ◽  
Vol 30 (5) ◽  
pp. 639-646 ◽  
Author(s):  
T. Naranjo ◽  
A. Roca ◽  
R. Giraldez ◽  
P. G. Goicoechea

Metaphase I pairing was studied in five ph1b mutant wheat × rye hybrids to verify the presence of translocations between homoeologous chromosomes in ph1b mutant wheat and to establish the pairing homoeology between wheat and rye chromosomes. Three 5B-deficient ABDR hybrids with standard chromosome structure were used as controls. Chromosomes 1R and 5R of rye and most wheat chromosomes, as well as their arms, were identified by means of C-banding. The presence of 5BS in ph1b hybrids raised the overall pairing level. The pattern of pairing between wheat chromosomes in ph1b hybrids, as in 5B-deficient hybrids, was characterized by the occurrence of preferential pairing between chromosomes of the A and D genomes in most homoeologous groups. The existence of a double translocation involving 4BL, 5AL, and 7BS in common wheat was confirmed. Deviation from the standard pairing pattern suggested the existence of a translocation involving 1BL and 1DL in one ph1b ABDR plant and another translocation involving 3AL and 3DL in three other ph1b hybrids. In ph1b hybrids, wheat – rye pairing was relatively frequent for 1RL, 5RL, and an arm of a metacentric rye chromosome, probably 2R, that is homoeologous to 2BL, and the homoeologous arms of 2A and 2D. The existence of a translocation involving 5RL and 4RL in rye was confirmed.Key words: homoeologous, homologous, 5B-deficient, translocations, C-banding.


Genetics ◽  
2006 ◽  
Vol 174 (3) ◽  
pp. 1583-1596 ◽  
Author(s):  
Zhiqian Liu ◽  
Katarzyna Adamczyk ◽  
Maria Manzanares-Dauleux ◽  
Frédérique Eber ◽  
Marie-Odile Lucas ◽  
...  

Genome ◽  
1991 ◽  
Vol 34 (6) ◽  
pp. 929-934 ◽  
Author(s):  
P. Banks ◽  
E. J. Britten ◽  
G. H. Gordon

Germinating seeds of rape (Brassica napus L.) and of tomato (Lycopersicon esculentum Mill.), and 1-month-old tomato seedlings, were treated with para-fluorophenylalanine to change chromosome numbers. A number of morphological aberrations were found in treated plants of both species, some of which were also observed in progeny of treated tomatoes. Aneuploids and polyploids were confirmed cytologically in treated plants of both species. The investigations confirm the suggestion previously made for maize, that para-fluorophenylalanine is capable of changing chromosome numbers and the resulting morphology of plants of widely different phylogenetic categories.Key words: Para-fluorophenylalanine, chromosome number changes, plants, tomato, rape, aneuploids, polyploids, morphological changes.


Genome ◽  
1989 ◽  
Vol 32 (3) ◽  
pp. 408-413 ◽  
Author(s):  
J. Jahier ◽  
A. M. Chèvre ◽  
A. M. Tanguy ◽  
F. Eber

The hybrid Brassica napus × B. nigra was produced and backcrossed three times to rapeseed. BC3 genotypes with one or two additional chromosomes were either selfed or haplodiploidized by using anther culture followed by colchicine doubling. Thirty-four fertile disomic addition lines have so far been obtained. Meiotic pairing in most of them was close to 20 II at metaphase I of meiosis. Their characterization is in progress. This material obtained for the first time in B. napus should be of great interest in the study of genome structure and basic chromosome number in Brassica species.Key words: Brassica, genome, disomic addition lines, meiotic behaviour.


Genetics ◽  
1974 ◽  
Vol 78 (1) ◽  
pp. 193-203
Author(s):  
Ralph Riley

ABSTRACT Meiotic chromosome pairing in Triticum aestivum is controlled by genetic systems promoting and reducing pairing. The pairing of homoeologous chromosomes is prevented principally by the activity of a single locus (Ph) distally located on the long arm of chromosome 5B. In certain hybrids, supernumerary chromosomes (B chromosomes) from Aegilops species can compensate for the absence of chromosome 5B preventing or reducing homoeologous pairing. Temperature-dependent variants and colchicine sensitivity have been used to show that there are at least two stages in the G1 of meiosis at which the occurrence of meiotic pairing is determined. Wheat may differ from lily in the detailed organization of meiosis.


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