New cytogenetic information on Allium iranicum (Alliaceae) from Iran

Biologia ◽  
2006 ◽  
Vol 61 (4) ◽  
Author(s):  
Seyed Ghaffari

AbstractKaryotype analysis and chromosome behaviour in tetraploid Allium iranicum is reported. The somatic karyotype 2n = 32, consists of 12 pairs of metacentric chromosomes, two pairs of submetacentric chromosomes and two pairs of submetacentric satellite chromosomes. Chromosome complement follows two sets of 16 pairs of homologous chromosomes. A detailed analysis of Pachytene, Diplotene and Metaphase I of meiosis in pollen mother cells in this taxon showed that the most common chromosome configurations were bivalents at all subphases mentioned. It is concluded that A. iranicum is most likely a natural allotetraploid and certainly differs from related species A. ampeloprasum, A. commutatum and A. porrum.

Genome ◽  
1987 ◽  
Vol 29 (1) ◽  
pp. 63-66 ◽  
Author(s):  
Batia Pazy ◽  
Uzi Plitmann

Idiosyncratic chromosome behaviour during meiosis was found in pollen mother cells of Cuscuta babylonica Choisy, a thread-like holoparasitic herb. Its main features are among the following: (i) telomeric association between homologues through most stages of the process, which leads to persisting chromatid bivalents (= "demibivalents"); (ii) uncommon chromosome segregation in first and second anaphase; and (iii) prolonged intensified heterochromatinization. Although "regular" in its own way, this process leads to the formation of unviable products. Its further investigation might contribute to our understanding of the role of the spindle and chromosome movement in the ordinary process of meiosis. Key words: meiosis (abnormal), persisting demibivalents, Cuscuta babylonica.


1941 ◽  
Vol 19c (9) ◽  
pp. 351-369 ◽  
Author(s):  
R. Merton Love

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.


2020 ◽  
Vol 71 (22) ◽  
pp. 7046-7058 ◽  
Author(s):  
Ian Fayos ◽  
Anne Cécile Meunier ◽  
Aurore Vernet ◽  
Sergi Navarro-Sanz ◽  
Murielle Portefaix ◽  
...  

Abstract In Arabidopsis, chromosomal double-strand breaks at meiosis are presumably catalyzed by two distinct SPO11 transesterases, AtSPO11-1 and AtSPO11-2, together with M-TOPVIB. To clarify the roles of the SPO11 paralogs in rice, we used CRISPR/Cas9 mutagenesis to produce null biallelic mutants in OsSPO11-1, OsSPO11-2, and OsSPO11-4. Similar to Osspo11-1, biallelic mutations in the first exon of OsSPO11-2 led to complete panicle sterility. Conversely, all Osspo11-4 biallelic mutants were fertile. To generate segregating Osspo11-2 mutant lines, we developed a strategy based on dual intron targeting. Similar to Osspo11-1, the pollen mother cells of Osspo11-2 progeny plants showed an absence of bivalent formation at metaphase I, aberrant segregation of homologous chromosomes, and formation of non-viable tetrads. In contrast, the chromosome behavior in Osspo11-4 male meiocytes was indistinguishable from that in the wild type. While similar numbers of OsDMC1 foci were revealed by immunostaining in wild-type and Osspo11-4 prophase pollen mother cells (114 and 101, respectively), a surprisingly high number (85) of foci was observed in the sterile Osspo11-2 mutant, indicative of a divergent function between OsSPO11-1 and OsSPO11-2. This study demonstrates that whereas OsSPO11-1 and OsSPO11-2 are the likely orthologs of AtSPO11-1 and AtSPO11-2, OsSPO11-4 has no major role in wild-type rice meiosis.


1990 ◽  
Vol 97 (3) ◽  
pp. 565-570
Author(s):  
JANET M. MOSS ◽  
BRIAN G. MURRAY

Pollen mother cells at metaphase I have been reconstructed from serial sections in normal and interchange heterozygotes of Briza humilis. The pollen mother cells have an irregular shape with a prominent projection from the tangential face into the anther loculus. The seven bivalents of the normal plant are usually arranged with one bivalent in a central position surrounded by a ring of the remaining six or as a ring of all seven bivalents. The central:peripheral distribution of quadrivalents is different in two different interchange plants; in a sector analysis, where cells are divided into four quarters relative to the tangential face of the pollen mother cell, the two plants also show differences in quadrivalent distribution, indicating that individual chromosomes occupy different positions in the cell. The relevance of these results to the positioning of quadrivalents in lateral squashes of meiotic metaphase I are discussed.


Genome ◽  
1994 ◽  
Vol 37 (2) ◽  
pp. 181-189 ◽  
Author(s):  
Huw M. Thomas ◽  
Barry J. Thomas

A spreading technique for synaptonemal complexes (SCs) was applied to pollen mother cells of two aneuploid genotypes of autotriploid Lolium multiflorum (2n = 3x + 1 = 22). In the earliest nuclei analyzed the axial elements are in six groups of 3 and one group of 4. Most groups have formed multivalents with from one to five pairing partner exchanges, but there are also groups that have formed bivalents and univalents. Some axial elements have formed triple associations, in one case for the length of the trivalent. Unsynapsed axial elements remain aligned with their homologous SCs into pachytene, but this alignment is abolished as these axes pair heterologously among themselves until the entire axial element complement is synapsed. At metaphase I most chromosomes are associated as trivalents and quadrivalents.Key words: Lolium, triploid, pairing partner exchange, chiasma, multivalent.


Genome ◽  
2001 ◽  
Vol 44 (4) ◽  
pp. 738-741 ◽  
Author(s):  
B F Cheng ◽  
G Séguin-Swartz ◽  
D J Somers ◽  
G Rakow

The low glucosinolate Brassica juncea breeding line 1058 was derived from a BC1F3 plant of an interspecific cross between high glucosinolate Indian B. juncea (genome AABB, 2n = 36) line 60143 and B. rapa (genome AA, 2n = 20) canola strain CZY. Line 60143 had 2n = 36 chromosomes (18 bivalents at metaphase I) and strain CZY had 2n = 20 chromosomes (10 bivalents). Line 1058 was nullisomic, with 2n - 2 = 34 chromosomes, with 17 bivalents formed at metaphase I and an even chromosomal segregation of 17:17 at anaphase I. In F1 hybrid plants of the cross 1058 × CZY, 98.3% of the pollen mother cells had 10 bivalents and seven univalents. This is evidence that plants of line 1058 are nullisomic, missing one pair of B-genome chromosomes.Key words: low glucosinolate mustard, meiotic behaviour, cytogenetics.


1984 ◽  
Vol 26 (5) ◽  
pp. 519-522 ◽  
Author(s):  
Patrick E. McGuire

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.


2021 ◽  
Author(s):  
◽  
Kenneth George Ryan

<p>Reliable techniques for the living cell culture and correlative light and electron microscopy (EM) of meiotic pollen mother cells (PMCs) of Iris spuria, Allium triquetrum and Tradescantia flumenensis are described in detail. Living PMCs were successfully cultured in a slide chamber on agar/sucrose medium. Cells were covered with an inert oil to prevent their dehydration, and some cells were cultured from metaphase I to tetrad cell formation over a 20 hour period. Other PMCs were fixed with glutaraldehyde and flat embedded using a modification of the agar sandwich technique of Mole-Bajer and Bajer (1968). This technique was developed to permit the preselection of PMCs at known meiotic stages, for subsequent EM examination. Serial thin sections were cut at known planes of section; and 3-D reconstructions of MT distribution, and MT counts from transverse sections were completed. It was also possible to examine sections of an Iris anaphase I PMC which had been previously studied in life. Anaphase I and II chromosome velocities were analysed in the three species. Mean velocities were approximately 0.5 mu m/min with some variation from cell to cell and between sister half-spindles. In Allium anaphase I there was also variation in chromosome velocity within the half-spindle; and this variation was found not to be related to chromosome position on the metaphase I plate. Spindle elongation was zero in Allium anaphase I and in Iris anaphase II, but was detectable in Allium anaphase II (40%) and in "Iris anaphase I (l5%). The extent of spindle elongation in Tradescantia could not be determined. The kinetochore region in the first meiotic division consisted of two closely appressed, but structurally (and functionally) distinct, sister kinetochores. At meiosis II, the two sister kinetochores were separate from each other and faced opposite poles. The kinetochore arrangement probably changes from side-by-side (meiosis I) to back-to-back (meiosis II) during chromosome recondensation at prophase II in these cells. Bundles of non-kinetochore microtubules (nkMTs) span the interzone between sister chromosome units at metaphase I and II and anaphase II. Bundles of kinetochore MTs (kMTs) do not increase in divergence at any stage of meiosis studied; there was little interaction between nkMTs and kMTs, and MT-MT cross bridges were rare. These observations are not consistent with models of chromosome movement based on MT sliding or zipping. No relationship was found between nkMT distribution and spindle elongation, and the several different nkMT distributions which have been reported for other cell types may be variations on a structural theme. Spindle endoplasmic reticulum (ER) in meiosis II was found to be derived largely from invaginations and evaginations of the nuclear envelope. Growth of existing spindle ER was proposed to account for the doubling in the amount of ER observed between interphase and prometaphase II. Randomly oriented elements of ER, in early prometaphase II spindles may become passively aligned along the interpolar axis and then actively transported polewards at later stages of prometaphase II and metaphase II. Suggestions for future research are offered.</p>


Genome ◽  
1987 ◽  
Vol 29 (5) ◽  
pp. 765-769 ◽  
Author(s):  
Gary R. Bauchan ◽  
Li-Ching Wang Linkous ◽  
William Tai

An Agropyron cristatum plant (CB-9-41), crested wheat grass, and its vegetative clones have been identified that contain pollen mother cells that have a gain or a loss in chromatin (DNA). CB-9-41 was identified during the course of an experiment to determine the effectiveness of colchicine on the doubling of the chromosome complement. The seeds that produced this plant were presoaked and then treated with a 0.1% aqueous solution of colchicine for 12 h. All stages of meiosis were studied in the original colchicine-treated plant and three vegetative clones that were obtained 17 years later. Approximately 40% of the pollen mother cells had meiotic irregularities. These irregularities were caused by multipolar meiosis (23%), precocious separation of bivalents at metaphase (8%), inversions (6%), and cytomixis (11%). The gain or loss of chromatin occurred as a result of cytomixis. Key words: crested wheat grass, extragenomic chromatin, multipolar meiosis, colchicine.


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