The effect of colchicine on meiosis in the Rhoeo discolor stabile complex translocation heterozygote

Genome ◽  
1992 ◽  
Vol 35 (4) ◽  
pp. 611-613 ◽  
Author(s):  
R. C. Verma ◽  
P. Vyas ◽  
S. N. Raina
Keyword(s):  
Chromosome Pairing ◽  
Translocation Heterozygote ◽  
Complex Translocation ◽  
Complete Chain ◽  
Chain Complexes ◽  
Metaphase I

Rhoeo discolor (2n = 12) was used to study the effect of colchicine on chromosome pairing during meiosis. Pachytene pairing appeared unaffected, but only 17.5% of the PMCs formed a ring of 12 chromosomes at metaphase I of meiosis. While 27.5% of cells had a complete chain of 12, 49.0% had chain configurations of varying (2–11) number of chromosomes and 6.0% had complete univalence. Adjacent orientation was found in the majority of cells with chain complexes of 2–11 chromosomes. The result was highly disturbed anaphase I where 58.4% PMCs were abnormal. It is concluded that the presence of aberrant cells at metaphase I is either due to colchicine-induced ineffectiveness of pairing at the very small pairing regions or failure of chiasma formation.Key words: colchicine, meiosis, Rhoeo discolor, translocation heterozygote, univalents, alternate/adjacent orientation.

Chromosomal fusion and meiotic behaviour in Delena cancerides (Araneae: Sparassidae). I. Chromosome pairing and X-chromosome segregation

Genome ◽  
1991 ◽  
Vol 34 (4) ◽  
pp. 561-566 ◽  
Author(s):  
D. M. Rowell
Keyword(s):  
Synaptonemal Complex ◽  
Chromosome Segregation ◽  
X Chromosome ◽  
Chromosome Pairing ◽  
X Chromosomes ◽  
Translocation Heterozygote ◽  
Complex Translocation ◽  
Monobrachial Homology ◽  
Pairing Initiation ◽  
Surface Spreading

Surface spreading of meiotic material in Delena cancerides indicates that pairing initiation among metacentric chromosomes with monobrachial homology differs from that of telocentric forms and free metacentric bivalents and results in a star-shaped structure at pachytene. Distance cosegregation of the three X chromosomes in ancestral, telocentric forms is prefaced by a centric association early in prophase I. This centric association of the X chromosomes is conserved in metacentric races despite the presence of an X-autosome fusion.Key words: synaptonemal complex, translocation heterozygote, X chromosome, spider.

CHROMOSOME PAIRING IN TWO INTERSPECIFIC HYBRIDS OF TRIFOLIUM

1970 ◽  
Vol 12 (4) ◽  
pp. 790-794 ◽  
Author(s):  
Chi-Chang Chen ◽  
Pryce B. Gibson
Keyword(s):  
Phylogenetic Relationship ◽  
Chromosome Pairing ◽  
Trifolium Repens ◽  
Interspecific Hybrids ◽  
Triploid Hybrid ◽  
Close Phylogenetic Relationship ◽  
Metaphase I

Both Trifolium repens (2n = 32) and T. nigrescens (2n = 16) formed bivalents during meiosis. However, their triploid hybrid showed an average of 4.27 trivalents per microsporocyte at metaphase I. The frequency of trivalents in the hybrid between T. nigrescens and autotetraploid T. occidentale (2n = 32) was 5.69. The data are interpreted to indicate: (1) a possible autotetraploid origin of T. repens; and (2) a close phylogenetic relationship among T. repens, T. nigrescens and T. occidentale.

Chromosome pairing and potential for intergeneric recombination in some hypotetraploid somatic hybrids of Lycopersicon esculentum (+) Solanum tuberosum

Genome ◽  
1993 ◽  
Vol 36 (6) ◽  
pp. 1032-1041 ◽  
Author(s):  
J. H. de Jong ◽  
A. M. A. Wolters ◽  
J. M. Kok ◽  
H. Verhaar ◽  
J. van Eden
Keyword(s):  
Solanum Tuberosum ◽  
Lycopersicon Esculentum ◽  
Synaptonemal Complex ◽  
Chromosome Pairing ◽  
Somatic Hybrids ◽  
Cytogenetic Study ◽  
Unreduced Gametes ◽  
Root Tip ◽  
Prophase I ◽  
Metaphase I

Three somatic hybrids resulting from protoplast fusions of a diploid kanamycin-resistant line of tomato (Lycopersicon esculentum) and a dihaploid hygromycin-resistant transformant of a monohaploid potato (Solanum tuberosum) line were used for a cytogenetic study on chromosome pairing and meiotic recombination. Chromosome counts in root-tip meristem cells revealed two hypotetraploids with chromosome complements of 2n = 46 and one with 2n = 47. Electron microscope analyses of synaptonemal complex spreads of hypotonically burst protoplasts at mid prophase I showed abundant exchanges of pairing partners in multivalents involving as many as eight chromosomes. In the cells at late pachytene recombination nodules were found in multivalents on both sides of pairing partner exchanges, indicating recombination at both homologous and homoeologous sites. Light microscope observations of pollen mother cells at late diakinesis and metaphase I also revealed multivalents, though their occurrence in low frequencies betrays the reduction of multivalent number and complexity. Precocious separation of half bivalents at metaphase I and lagging of univalents at anaphase I were observed frequently. Bridges, which may result from an apparent inversion loop found in the synaptonemal complexes of a mid prophase I nucleus, were also quite common at anaphase I, though the expected accompanying fragments could be detected in only a few cells. Most striking were the high frequencies of first division restitution in preparations at metaphase II/anaphase II, giving rise to unreduced gametes. In spite of the expected high numbers of balanced haploid and diploid gametes, male fertility, as revealed by pollen staining, was found to be negligible.Key words: synaptonemal complex, recombination, chromosome pairing, somatic hybrid, Lycopersicon esculentum (+) Solanum tuberosum.

Analysis of synaptonemal complexes and chromosome pairing at metaphase I in the diploid intergeneric hybrid Lolium multiflorum × Festuca drymeja

Genome ◽  
1990 ◽  
Vol 33 (4) ◽  
pp. 465-471 ◽  
Author(s):  
Hum M. Thomas ◽  
W. G. Morgan
Keyword(s):  
Chromosome Pairing ◽  
Complex Analysis ◽  
Lolium Multiflorum ◽  
Intergeneric Hybrid ◽  
Chiasma Formation ◽  
Genotypic Effect ◽  
Synaptonemal Complexes ◽  
Dna Values ◽  
Synaptonemal Complex Analysis ◽  
Metaphase I

The synaptonemal complexes in the diploid hybrid Lolium multiflorum × Festuca drymeja were examined by the surface spreading technique, and chromosome pairing at metaphase I was analysed. Synaptonemal complex analysis revealed "illegitimate" pairing, including multivalents and foldback pairing. At metaphase I, most chiasmata were between chromosomes of the same genome, and again multivalents were found. It was concluded that most synaptonemal complexes resulted in chiasma formation. The effects of the large differences in DNA values of the two species and the possible genotypic effect of F. drymeja on chromosome pairing are discussed.Key words: Lolium-Festuca, synaptonemal complexes, nonhomologous pairing, DNA values.

Genome constitution of the Australian hexaploid grass Elymus scabrus (Poaceae: Triticeae)

Genome ◽  
1993 ◽  
Vol 36 (1) ◽  
pp. 147-151 ◽  
Author(s):  
J. Torabinejad ◽  
R. J. Mueller
Keyword(s):  
Chromosome Pairing ◽  
Interspecific Hybrids ◽  
Intergeneric Hybrid ◽  
Meiotic Pairing ◽  
Genome Constitution ◽  
Psathyrostachys Juncea ◽  
Hybrid Plants ◽  
Thinopyrum Bessarabicum ◽  
Mother Cells ◽  
Metaphase I

Eight intergeneric hybrid plants were obtained between Elymus scabrus (2n = 6x = 42, SSYY??) and Australopyrum pectinatum ssp. retrofractum (2n = 2x = 14, WW). The hybrids were vegetatively vigorous but reproductively sterile. Examination of pollen mother cells at metaphase I revealed an average of 16.63 I, 5.29 II, 0.19 III, and 0.05 IV per cell for the eight hybrids. The average chiasma frequency of 6.77 per cell in the above hybrids strongly supports the presence of a W genome from A. pectinatum ssp. retrofractum in E. scabrus. Meiotic pairing data of some other interspecific hybrids suggest the existence of the SY genomes in E. scabrus. Therefore, the genome constitution of E. scabrus should be written as SSYYWW. Two other hybrid plants resulted from Elymus yezoensis (2n = 4x = 28, SSYY) crosses with A. pectinatum ssp. pectinatum (2n = 2x = 14, WW). Both were weak and sterile. An average of 0.45 bivalents per cell were observed at metaphase I. This clearly indicates a lack of pairing between W genome of Australopyrum and S or Y genomes of E. yezoensis. In addition, six hybrid plants of E. scabrus with Psathyrostachys juncea (2n = 2x = 14, NN) and one with Thinopyrum bessarabicum (2n = 2x = 14, JJ) were also obtained. The average bivalents per cell formed in both combinations were 2.84 and 0.70, respectively. The results of the latter two combinations showed that there is no N or J genome in E. scabrus.Key words: wide hybridization, chromosome pairing, genome analysis, Australopyrum, Elymus.

Interlocked bivalents in reconstructed metaphase I cells of bread wheat

1985 ◽  
Vol 75 (1) ◽  
pp. 85-92
Author(s):  
J.S. Heslop-Harrison ◽  
M.D. Bennett
Keyword(s):  
Triticum Aestivum ◽  
Light Microscopy ◽  
Bread Wheat ◽  
Chromosome Pairing ◽  
Light Microscope ◽  
Serial Sections ◽  
Ring Bivalents ◽  
Mother Cells ◽  
I Cells ◽  
Metaphase I

Complete reconstructions of all the bivalents were made from electron micrographs of serial sections through six pollen mother cells at metaphase I of meiosis in Triticum aestivum (hexaploid bread wheat). At least two of these metaphases contained interlocked pairs of bivalents. In one, two ring bivalents were interlocked, while in another a rod bivalent ran through the centre of a ring bivalent. Two other groups of bivalents were too closely appressed to allow separation into individual bivalents and may have contained interlocks. Meiosis in other anthers of the same plants examined by light microscopy was considered normal. The frequency of interlocking found was much higher than reported from light-microscope spreads. Not all interlocks in metaphase I cells need adversely affect meiosis, but knowledge of their regularity and form may facilitate understanding the processes of chromosome pairing.

Homology of chromosomes of the X genomes in common and Uruguayan dallisgrass, Paspalum dilatatum

Genome ◽  
1991 ◽  
Vol 34 (6) ◽  
pp. 950-953 ◽  
Author(s):  
Byron L. Burson
Keyword(s):  
Chromosome Pairing ◽  
Chromosome Numbers ◽  
The Other ◽  
Paspalum Dilatatum ◽  
Intraspecific Hybridization ◽  
The Common ◽  
Complete Sets ◽  
The Relationship ◽  
Metaphase I

Two biotypes of dallisgrass, Paspalum dilatatum Poir., designated common and Uruguayan, have chromosome numbers and genome formulas of 2n = 5x = 50 (IIJJX) and 2n = 6x = 60 (IIJJXX), respectively. The relationship between the X genomes in these two biotypes is unknown, and each was arbitrarily assigned the letter X to designate an unknown genome. This study was undertaken to determine the relationship between the X genomes in these two biotypes. Because both biotypes are apomicts and cannot be crossed, a sexual intraspecific F1 hybrid (2n = 45) between sexual yellow-anthered (2n = 4x = 40; IIJJ) and common dallisgrass biotypes was crossed with Uruguayan dallisgrass. This F1 hybrid has complete sets of the I and J genomes but only 5 of the 10 chromosomes of the X genome from common dallisgrass. Two hybrids were recovered. One had 52 and the other had 53 chromosomes, which associated at metaphase I as 22 bivalents + 8 univalents and 23 bivalents + 7 univalents, respectively. Twenty bivalents represent pairing of members of the I and J genomes, and those in excess of 20 represent pairing between members of the two X genomes. The remaining members of the X genome from the Uruguayan biotype were present as univalents at metaphase I. This demonstrates that those chromosomes of the X genome from the common biotype that were present are homologous to members of the X genome of the Uruguayan biotype. Both hybrids are aposporous facultative apomicts with some sterility.Key words: meiosis, intraspecific hybridization, chromosome pairing, genome relations, apomixis.

Metaphase I pairing of deficient chromosomes and genetic mapping of deficiency breakpoints in common wheat

Genome ◽  
1991 ◽  
Vol 34 (4) ◽  
pp. 553-560 ◽  
Author(s):  
C. A. Curtis ◽  
A. J. Lukaszewski ◽  
M. Chrzastek
Keyword(s):  
Triticum Aestivum ◽  
Genetic Mapping ◽  
Chromosome Pairing ◽  
Triticum Aestivum L ◽  
Genetic Distances ◽  
Homologous Chromosomes ◽  
Transmission Rates ◽  
Chromosome 5B ◽  
Pairing Initiation ◽  
Metaphase I

Metaphase I pairing of deficient chromosomes was analyzed in a set of 'Chinese Spring' (CS) wheat (Triticum aestivum L. em. Thell.) plants with varying lengths of deficiencies in the long arm of chromosome 4A (6, 8, 11, 17, 23, 34, 36, 39, and 50% missing), the long arm of chromosome 5B (49% missing), and the long arm of chromosome 2B (33% missing). Pairing in homologous chromosomes between deficient and complete arms was greatly reduced even by small differences in arm length. In deficiency homozygotes and in an isochromosome derived from a deficient 4AL arm, pairing of the two deficient arms was high and approached that of two complete arms. In plants where deficient and complete arms competed for pairing partners, pairing was exclusively between arms of the same length. These results suggest that in wheat, pairing initiation sites are distributed throughout at least the distal halves of the arms and that the alignment of telomeres may be critical for pairing success. Genetic mapping of the deficiency breakpoints was confounded by misdivision of unpaired chromosomes and abnormal transmission rates. Genetic distances between centromeres and breakpoints appeared to be proportional to metaphase I pairing frequencies.Key words: bread wheat, deficiency, chromosome pairing competition, mapping, telomere, pairing initiation.

Chromosome pairing in hybrids of ph1b mutant wheat with rye

Genome ◽  
1988 ◽  
Vol 30 (5) ◽  
pp. 639-646 ◽  
Author(s):  
T. Naranjo ◽  
A. Roca ◽  
R. Giraldez ◽  
P. G. Goicoechea
Keyword(s):  
Common Wheat ◽  
Chromosome Pairing ◽  
Chromosome Structure ◽  
Preferential Pairing ◽  
C Banding ◽  
Homoeologous Chromosomes ◽  
Metaphase I

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.

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