Genetically controlled desynapsis in diploid Critesion violaceum and its hybrids with autotetraploid Psathyrostachys juncea

1984 ◽  
Vol 26 (5) ◽  
pp. 532-537 ◽  
Author(s):  
Richard R-C. Wang
Keyword(s):  
Chromosome Pairing ◽  
Chiasma Frequency ◽  
Intergeneric Hybrid ◽  
Dosage Effect ◽  
The Other ◽  
Pollen Mother Cells ◽  
Psathyrostachys Juncea ◽  
Self Pollination ◽  
Meiotic Irregularities ◽  
Mother Cells

Segregation for chiasma frequency was observed in the progeny of a diploid (2n = 14) Critesion violaceum strain following self-pollination. One S1 plant had normal metaphase pairing with an average of 0.43I + 6.78II, giving a high chiasma frequency, 12.03 per cell. The other S1 plant averaged 7.89I + 3.08II and a low chiasma frequency, 3.47 per cell. Examination of pollen mother cells at early prophases revealed that chromosome pairing was not totally prevented. It was concluded that desynapsis was responsible for the meiotic irregularities observed in the variant progeny. The same phenomena were observed in F1 hybrids of the cross between diploid C. violaceum and an induced autotetraploid (2n = 28), Psathyrostachys juncea. The normal F1 hybrid had a chiasma frequency of 12.81, but the desynaptic hybrid had a chiasma frequency of 6.94. A dosage effect of the desynaptic gene, which was probably recessive, was suggested. The implications and significance of this discovery are discussed.Key words: asynapsis, chiasma, meiosis, intergeneric hybrid.

Coenocytism, ameiosis, and chromosome diminution in intergeneric hybrids in the perennial Triticeae

Genome ◽  
1988 ◽  
Vol 30 (5) ◽  
pp. 766-775 ◽  
Author(s):  
Richard R.-C. Wang
Keyword(s):  
Intergeneric Hybrid ◽  
Chromosome Elimination ◽  
Intergeneric Hybrids ◽  
Pollen Grain ◽  
Unreduced Gamete ◽  
Pollen Mother Cells ◽  
Psathyrostachys Juncea ◽  
Hybrid Plants ◽  
Mother Cells ◽  
Pollen Grain Wall

Three different pathways of ameiotic microsporogenesis were observed in some intergeneric hybrids of the perennial Triticeae grasses. In one of the hybrids between Pseudoroegneria spicata ssp. inermis and Psathyrostachys juncea, pollen mother cells remained as premeiotic interphase cells when the pollen grain wall started to form. The microspores in such an ameiotic plant are presumably unreduced. Coenocyte formation coupled with ameiosis occurred in two hybrid plants of Psathyrostachys huashanica × Secale montanum. Less than 10% of the pollen mother cells had one nucleus. An average of 4.44 nuclei, ranging from 1 to 25 per pollen mother cell, was observed. The nuclei in coenocytes remained unfused when the pollen grain wall was formed. Nucleus splitting followed by cytoplasmic budding or cleavage, possibly a process of chromosome diminution or elimination, replaced meiotic divisions in most of the pollen mother cells in one plant of Leymus angustus × Hordeum bulbosum and two plants of Thinopyrum elongatum × Psathyrostachys juncea. It is evident that these meiotic abnormalities are under genetic control. Probable locations for these genes controlling these phenomena are suggested.Key words: coenocyte, ameiosis, chromosome diminution, chromosome elimination, microsporogenesis, unreduced gamete, polyploidy, intergeneric hybrid.

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.

CHROMOSOME BEHAVIOUR IN F1 WHEAT HYBRIDS: I. PENTAPLOIDS

1941 ◽  
Vol 19c (9) ◽  
pp. 351-369 ◽  
Author(s):  
R. Merton Love
Keyword(s):  
The Other ◽  
Spindle Fibre ◽  
Chromosome Behaviour ◽  
Pollen Mother Cells ◽  
Triticum Vulgare ◽  
Attachment Region ◽  
Wheat Hybrids ◽  
Mother Cells ◽  
Relationship Of ◽  
Fibre Attachment

Meiosis was studied in varieties of Triticum vulgare (2n = 42), T. dicoccum (2n = 28), T. durum (2n = 28), T. Timopheevi (2n = 28), and in 16 of their pentaploid hybrids as part of a study in an attempt to establish criteria indicating relationships between 42- and 28-chromosome wheats, with particular reference to the possible relationship of the new 42-chromosome wheat, McMurachy's Selection, to T. dicoccum or T. durum.One plant each of T. vulgare var. Hope and Marquillo had only 41 chromosomes. One plant of T. durum var. Pentad had three times as many unpaired chromosomes as the other plants of this variety.A nucleus with 14 pairs and 7 univalents was not detected among the 86 pollen mother cells analysed in the cross involving T. Timopheevi. In the remaining crosses the frequency of this association of chromosomes was lowest in the three hybrids involving T. durum var. Pentad, greater in the three involving T. dicoccum var. Khapli, still greater in the three involving T. dicoccum var. Vernal, and greatest in the nine hybrids involving T. durum var. Iumillo.Of the seven "extra chromosomes" of T. vulgare only six remained unpaired in some pollen mother cells of the hybrids involving Vernal or Iumillo and five in those involving Khapli or Pentad. One pollen mother cell of F1 Marquis × Pentad contained only four unpaired chromosomes.Associations of four chromosomes were rare in some, and not seen at all in others, of the hybrids involving Vernal or Iumillo, more frequent in hybrids involving Khapli, and very frequent in hybrids involving Pentad. In the latter, from 47 to 57% of the nuclei had from one to three such multiple associations, and even chains of five and six chromosomes were observed.Fragmentation of unpaired chromosomes at or in the spindle fibre attachment region was observed in a number of first anaphase figures.There were statistically significant differences in the frequencies of occurrence of micronuclei in tetrads of the 15 hybrids studied at the second reduction division.The crosses R.L. 1544 (genetically related to T. durum var. Iumillo) × Iumillo and Hope (genetically related to T. dicoccum var. Vernal) × Vernal were used as standards for comparison. On the basis of the results, the following criteria were used in attempting to establish relationships between the other 42- and 28-chromosome wheats: (1) the percentage of pollen mother cells with 14 pairs and 7 univalents (greatest in the hybrids between related varieties); (2) the average number of chromosomes involved in multiple associations (lowest in hybrids between related varieties); (3) fertility (greatest in hybrids between related varieties). McMurachy's Selection appeared to be most closely related to T. durum var. Iumillo. On the basis of Criteria (1) and (2), Marquis appears to be more closely related to T. dicoccum var. Vernal than to T. durum var. Iumillo, but in respect of fertility it seems closer to the latter.Chromosome behaviour in the 16 hybrids cannot be neatly summarized. Even varieties within a species gave different results—results that are not in agreement with earlier published reports on chromosome behaviour in pentaploid wheat hybrids in which it has been stated that 14 bivalents and 7 univalents are most commonly found. The difficulties encountered in attempting to establish criteria indicating relationships between the 42- and 28-chromosome wheats suggest that the utmost caution must be used in drawing phylogenetic conclusions on the basis of such data.

scholarly journals Meiosis in Oenothera missouriensis

1933 ◽  
Vol 113 (780) ◽  
pp. 57-70 ◽  
Keyword(s):  
Chromosome Pairing ◽  
Cytological Study ◽  
Stage Ii ◽  
Species Hybrid ◽  
Final Solution ◽  
Pollen Mother Cells ◽  
Closed Circle ◽  
Somatic Number ◽  
Mother Cells ◽  
Species Hybrids

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 .

Genetic control of meiosis in rice, Oryza sativa L. IV. Cytogenetical analyses of asynaptic mutants

1984 ◽  
Vol 26 (3) ◽  
pp. 264-271 ◽  
Author(s):  
Kunio Kitada ◽  
Takeshi Omura
Keyword(s):  
Oryza Sativa ◽  
Genetic Control ◽  
Chromosome Pairing ◽  
Chiasma Frequency ◽  
Oryza Sativa L ◽  
Recessive Gene ◽  
The Other ◽  
Normal Plant ◽  
Meiotic Stage ◽  
The Mean

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.

The Effect of Spindle Inhibitors Applied before Meiosis on Meiotic Chromosome Pairing

1973 ◽  
Vol 12 (1) ◽  
pp. 143-161 ◽  
Author(s):  
G. A. DOVER ◽  
R. RILEY
Keyword(s):  
Chromosome Pairing ◽  
Chloral Hydrate ◽  
Control Mechanism ◽  
Meiotic Chromosome ◽  
Chiasma Formation ◽  
Meiotic Pairing ◽  
Mitotic Spindles ◽  
Pollen Mother Cells ◽  
Meiotic Chromosome Pairing ◽  
Mother Cells

Injection of 0.5% colchicine into immature tillers of genotypes of Triticum aestivum, T. aestivum x Aegilops mutica and T. aestivum x Secale cereale hybrids induces asynapsis at first meiotic metaphase irrespective of the homologous or homoeologous nature of the potential pairing chromosomes. The induction of asynapsis occurs at a time during and immediately following the last premeiotic mitosis of pollen mother cells. No disruption of synapsis and chiasma formation occurs in anthers having pollen mother cells originally at leptotene or immediately prior to leptotene when cultured in White's medium plus colchicine. Tetraploid and octaploid pollen mother cells resulting from the disruption of premeiotic spindles by colchicine show pairing of chromosomes only in bivalents, in genotypes normally having a degree of multivalent pairing configurations. The induction of multipolar mitotic spindles with 0.01% colchicine results in the development of pollen mother cell mosaics with different numbers of chromosomes. Such cells show high levels of chromosome pairing, including multivalents, in some genotypes that normally have very little chromosome pairing. The injection of 0.5% chloral hydrate during the last premeiotic mitosis of the archesporium causes no disturbances of meiotic pairing. The results are discussed with reference to the hypothesis that the control mechanism of meiotic chromosome pairing involves centromeric microtubules of the spindle (not affected by chloral hydrate) that are responsible for the positional adjustment, during the last mitotic anaphase, of potential pairing partners.

Genomic constitution of the allo-octoploid Elymus tenuis (Poaceae: Triticeae) of New Zealand

2010 ◽  
Vol 23 (5) ◽  
pp. 381 ◽  
Author(s):  
Hai-Qin Zhang ◽  
Xue Bai ◽  
Bao-Rong Lu ◽  
Henry E. Connor ◽  
Yong-Hong Zhou
Keyword(s):  
New Zealand ◽  
Chromosome Pairing ◽  
Interspecific Hybrids ◽  
Genomic Constitution ◽  
Pollen Mother Cells ◽  
Mother Cells

Elymus tenuis (Buch.) Á.Löve et Connor is a perennial octoploid (2n = 56) wheatgrass endemic to New Zealand. To investigate its genomic constitution, four artificial interspecific hybrids between E. tenuis and E. enysii (2n = 4x = 28, HW), and E. solandri (2n = 6x = 42, StYW) and E. multiflorus (2n = 6x = 42, StYW) were studied cytologically. Meioses in pollen mother cells (PMCs) of the hybrids showed relatively high chromosome pairing, with an average of 13.50 in E. enysii × E. tenuis, 20.22 in E. solandri × E. tenuis, 19.62 in E. multiflorus × E. tenuis, and 20.00 in E. tenuis × E. multiflorus bivalents per cell, respectively. The results indicate that E. tenuis is an allo-octoploid species, with the new and unique genomic constitution StYHW. An autochthonous origin is proposed for it.

Differences in meiotic pairing induction between the A genomes of Triticum boeoticum Boiss. and T. urartu Tum. using diploid species of the subtribe Triticineae as analysers

Genome ◽  
1987 ◽  
Vol 29 (6) ◽  
pp. 891-893 ◽  
Author(s):  
H. Lucas ◽  
J. Jahier
Keyword(s):  
Interspecific Hybrids ◽  
Diploid Species ◽  
Distinct Species ◽  
The Other ◽  
Meiotic Behaviour ◽  
Meiotic Pairing ◽  
Haynaldia Villosa ◽  
Pollen Mother Cells ◽  
Triticum Boeoticum ◽  
Mother Cells

The number of associations between chromosome arms in the pollen mother cells of the hybrid Triticum boeoticum × T. urartu is similar to that in the pollen mother cells of the parental accessions. The latter two species were crossed with the following diploid species: T. tauschii, T. comosum, T. umbellulatum, and Haynaldia villosa. The meiotic behaviour of the hybrids showed that the chromosomes of T. urartu share more homology with the diploid Triticum species than do those of T. boeoticum. On the other hand, there is more pairing in the hybrid T. boeoticum × H. villosa than in T. urartu × H. villosa. These results confirm that T. boeoticum and T. urartu are distinct species. Key words: Triticineae, interspecific hybrids, meiotic behaviour, speciation.

Ultrastructure of meiotic pairing in B chromosomes of Crepis capillaris. I. One-B and two-B pollen mother cells

Genome ◽  
1989 ◽  
Vol 32 (4) ◽  
pp. 611-621 ◽  
Author(s):  
G. H. Jones ◽  
J. A. F. Whitehorn ◽  
S. M. Albini
Keyword(s):  
Synaptonemal Complex ◽  
Chromosome Pairing ◽  
Complex Surface ◽  
B Chromosome ◽  
B Chromosomes ◽  
Meiotic Pairing ◽  
Pollen Mother Cells ◽  
Crepis Capillaris ◽  
Axis Length ◽  
Mother Cells

Chromosome pairing of a small metacentric B chromosome in Crepis capillaris has been studied by synaptonemal complex surface spreading of pollen mother cells containing either one or two B chromosomes. The B-chromosome axis, on average, represents about 8.7% of the axis length of the standard A-chromosome set, which is less than the corresponding values for DNA content (10.6%) and mitotic chromosome volume (13.6%). Single B chromosomes commonly undergo fold-back pairing to give a symmetrical hairpin loop, which supports earlier suggestions that this B chromosome is an isochromosome. Two B chromosomes may show interarm pairing, exclusively, or interchromosome pairing, exclusively, or combinations of the two. Near the centromeres pairing occurs preferentially between arms of the same chromosome, but chromosome ends show random association. Some B chromosomes show anomalous pairing configurations, which may reflect further orders of reverse repeats within arms or, alternatively, nonhomologous pairing. The period of B-chromosome pairing is confined almost exclusively to zygotene, when the standard A chromosomes are pairing, but within this period their pairing is delayed relative to the A set. Individual B chromosomes at zygotene contain from one to three separate synaptonemal complex segments. These are widely distributed within the chromosomes, mainly in distal and interstitial regions; pairing is delayed around the centromere.Key words: B chromosomes, isochromosomes, synaptonemal complex.

Chromosome pairing in triploid and tetraploid hybrids in Elytrigia (Triticeae; Poaceae)

1984 ◽  
Vol 26 (5) ◽  
pp. 519-522 ◽  
Author(s):  
Patrick E. McGuire
Keyword(s):  
Chromosome Pairing ◽  
Genome Analysis ◽  
Triploid Hybrid ◽  
Pollen Mother Cells ◽  
Tetraploid Hybrid ◽  
A Genome ◽  
Mother Cells ◽  
Metaphase I

Mean chromosome pairing of 5.14I + 1.28II (rod) + 3.86II (ring) + 1.47III + 0.11IV (open) + 0.11V was observed in pollen mother cells at metaphase I in the triploid hybrid Elytrigia scirpea (K. Presl) Holub, 2n = 4x = 28 × E. bessarabica (Savul. et Rayss) Dubrovik, 2n = 4x = 14. Mean chromosome pairing of 3.71I + 2.29II (rod) + 1.82II (ring) + 2.64III + 0.29IV (open) was observed in the triploid hybrid E. curvifolia (Lange) Holub, 2n = 4x = 28 × E. bessarabica. Mean chromosome pairing of 3.00I + 0.93II (rod) + 1.57II (ring) + 1.36III + 1.79IV (open) + 1.I4IV (closed) + 0.79V was observed in the tetraploid hybrid E. junceiformis Löve et Löve, 2n = 4x = 28 × E. curvifolia. The first hybrid provides the first evidence by genome analysis that E. bessarabica possesses a genome (designated Eb) which is closely related to the genomes of E. scirpea (ES and ESC) and hence to the E genome of E. elongata (Host) Nevski, 2n = 2x = 14. The second and third hybrids provide the first evidence that the two genomes of E. curvifolia (designated EC and ECU) are related to the Eb genome of E. bessarabica and thus to the E genome of E. elongata.Key words: Elytrigia, homoeology, Triticum, phylogeny, triploid, tetraploid.

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