CYTOLOGY OF PASPALUM VIRGATUM AND ITS RELATIONSHIP WITH P. INTERMEDIUM AND P. JURGENSII

1982 ◽  
Vol 24 (2) ◽  
pp. 219-226 ◽  
Author(s):  
Byron L. Burson ◽  
Camilo L. Quarin

A cytological study revealed that Paspalum virgatum L. is sexual, meiotically stable, and has 2n = 4x = 40 chromosomes. Paspalum virgatum was crossed with P. intermedium Munro. ex Morong and P. jurgensii Hackel; both have 2n = 2x = 20 chromosomes. Six P. intermedium × P. virgatum, 2n = 3x = 30, hybrids were studied cytologically. Meiosis was irregular with a mean chromosome pairing of 11.68 univalents, 9.09 bivalents, 0.03 trivalents, and 0.002 quadrivalents per cell at metaphase I. This indicates that the two species have a homologous genome with some minute structural differences because some of the bivalents were not tightly synapsed. One hybrid, 2n = 3x = 30, was recovered from the P. jurgensii × P. virgatum cross. Meiosis was irregular with a mean pairing of 18.72 univalents, 5.70 bivalents, and 0.05 trivalents. These findings suggest that P. jurgensii and P. virgatum have a partially homologous genome. Because P. intermedium and P. jurgensii have the genome formulas II and JJ, respectively, the formula II J2J2 is proposed for P. virgatum.

1975 ◽  
Vol 17 (1) ◽  
pp. 121-123 ◽  
Author(s):  
George Fedak

Chromosome pairing at metaphase I and distribution at anaphase I were examined in 3 autotetraploid and 3 amphidiploid parents and their F1 hybrids and related to spike fertility of the respective plants. Structural differences translocated from the Hordeum leporinum chromosomes to H. vulgare did not significantly enhance preferential pairing and subsequent fertility in the latter as anticipated. Quadrivalent formation was not related but regular disjunction at anaphase I was related to spike fertility.


1970 ◽  
Vol 12 (4) ◽  
pp. 790-794 ◽  
Author(s):  
Chi-Chang Chen ◽  
Pryce B. Gibson

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.


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

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.


Genome ◽  
1990 ◽  
Vol 33 (4) ◽  
pp. 465-471 ◽  
Author(s):  
Hum M. Thomas ◽  
W. G. Morgan

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.


A cytological study of the meiotic phenomena in Oenothera may not need an excuse in spite of the exhaustive studies of the genus made by numerous competent cytologists of this century. Up to the present time, all the investigators of Oenothera cytology have been successful in establishing that the basic ( n ) number of chromosomes in this genus is 7; although tetraploid (Gates, 1911), triploid (Cathcheside, 1931), and trisomic numbers might occur either naturally (by mutation) or could be produced by experiment. It is also known that the somatic number of chromosomes corresponds with the number of chromosome bodies in the diakinesis and metaphase of the heterotypic division.. Thus in diploid Oenothera species, hybrid, or mutant at the diakinesis of pollen mother cells 14 chromosomes have been shown to exist, withouth any doubt, in the configuration of a closed circle, in 7 ring pairs, or a mixtrue of free pairs and closed circles. Mathematically, there are 15 possible configurations in which 14 chromosomes can arrange themselves in the form of closed circle, ring pairs, or a combination of ring pairs and closed circles (Cleland and Blakeslee, 1931; Darlington, 1931). Of these 15 Possible configurations 13 have already been reported in various Oenothera species, hybrids and mutants (Darlington, 1931). Regarding the origin and significance of these chromosome configurations invsestigators have not yet reached an agreed opinion. Apart from the genetical significance, the much disputed cytological question of parasynaptic and telosynaptic methods of chromosome pairing is yet far from a final solution. In oenothera both the methods of pairing have strong sup-porters in consideration of observed cytological facts. The fact are (i) the continuous spireme (in leptotene stage); (ii) the pachynema and the diakinesis consisting of the 14 chromosomes arranged end to end. This arragement, known as catenation of chromosomes, favours the telosynaptic rather than the parasynaptic union. Wheras (i) double threads at the prophase, (ii) the looping of the threads, and (iii) the half number of bodies (7 ring pairs) at the diakinesis support the parasynaptic method of pairing of chromosomes. The occurence of a complete catenation of 14 chromosomes in some Oenotheras and the presence of 7 free pairs in others naturally suggests the question-whether they can be correlated with the two methods of chromosome-pairing in the meiosis of Oenothera .


Genome ◽  
1993 ◽  
Vol 36 (1) ◽  
pp. 147-151 ◽  
Author(s):  
J. Torabinejad ◽  
R. J. Mueller

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.


1979 ◽  
Vol 21 (1) ◽  
pp. 65-71 ◽  
Author(s):  
K. C. Armstrong

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.


1985 ◽  
Vol 75 (1) ◽  
pp. 85-92
Author(s):  
J.S. Heslop-Harrison ◽  
M.D. Bennett

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.


Genome ◽  
1991 ◽  
Vol 34 (6) ◽  
pp. 950-953 ◽  
Author(s):  
Byron L. Burson

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.


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