Synaptonemal complex spreading in Allium. II. Tetraploid A. vineale

1986 ◽  
Vol 28 (5) ◽  
pp. 754-761 ◽  
Author(s):  
Josef Loidl

In tetraploid Allium vineale four homologous axes are closely aligned in unsynapsed regions at early zygotene. This alignment is brought about by intercalary and terminal associations. The intercalary association sites are possibly targets of forces for long distance attraction of homologues and potential pairing initiation sites. The terminal associations are mediated by dense spherules and result possibly from the attachment of the telomeres to the nuclear envelope. In pachytene the alignment is abolished and the four axes are synapsed two by two, resulting in bivalents or, owing to partner switches in the synapsed axes, in quadrivalents. From the number of partner switches per configuration the number of pairing initiation sites is estimated. Homologous alignment and synapsis are discussed, comparing them with the conditions in a triploid species, which were described in a previous paper.Key words: Allium vineale, synaptonemal complex, polyploids, chromosome pairing, meiosis.

Genome ◽  
1991 ◽  
Vol 34 (4) ◽  
pp. 561-566 ◽  
Author(s):  
D. M. Rowell

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.


1987 ◽  
Vol 87 (3) ◽  
pp. 439-448
Author(s):  
J. Loidl

In Allium ursinum meiotic pairing of homologues is always incomplete; a proximal region on each bivalent remains regularly unsynapsed even in late pachytene. The spatial correlation of the unsynapsed region with the kinetochore suggests that the kinetochore itself exerts an inhibitory effect on synapsis in its vicinity. This can be interpreted as the cytological basis of the ‘centromere effect’ on recombination in this species. Moreover, the high incidence of a pericentric inversion loop in a heterozygous chromosome pair shows that proximal pairing initiation is possible and that its failure cannot be responsible for pericentric asynapsis. The formation of the inversion loop is complicated by the need for two independent pairing initiation sites because synapsis cannot proceed across the pericentric region. It is proposed that the meiotic bouquet polarization helps in establishing the presynaptic alignment of the homologous sites within the inverted regions and hence to achieve a high rate of inversion loop formation. Thickenings of the axial/lateral elements are not distributed equally along the synaptonemal complex. They are underrepresented in unpaired axes but strikingly abundant at the borders with synapsed regions, suggesting their origin in the pairing forks during the process of synapsis. They are virtually always present at nucleolus-organizing regions and often they appear at corresponding sites on opposite lateral elements. Besides the thickenings several other kinds of axial deformities are present in unpaired axes.


2017 ◽  
Vol 216 (2) ◽  
pp. 393-408 ◽  
Author(s):  
Benjamin Alleva ◽  
Nathan Balukoff ◽  
Amy Peiper ◽  
Sarit Smolikove

In meiotic prophase I, homologous chromosome pairing is promoted through chromosome movement mediated by nuclear envelope proteins, microtubules, and dynein. After proper homologue pairing has been established, the synaptonemal complex (SC) assembles along the paired homologues, stabilizing their interaction and allowing for crossing over to occur. Previous studies have shown that perturbing chromosome movement leads to pairing defects and SC polycomplex formation. We show that FKB-6 plays a role in SC assembly and is required for timely pairing and proper double-strand break repair kinetics. FKB-6 localizes outside the nucleus, and in its absence, the microtubule network is altered. FKB-6 is required for proper movement of dynein, increasing resting time between movements. Attenuating chromosomal movement in fkb-6 mutants partially restores the defects in synapsis, in agreement with FKB-6 acting by decreasing chromosomal movement. Therefore, we suggest that FKB-6 plays a role in regulating dynein movement by preventing excess chromosome movement, which is essential for proper SC assembly and homologous chromosome pairing.


Genome ◽  
2001 ◽  
Vol 44 (1) ◽  
pp. 27-31 ◽  
Author(s):  
K Mekada ◽  
M Harada ◽  
L K Lin ◽  
K Koyasu ◽  
P M Borodin ◽  
...  

Pairing of X and Y chromosomes at meiotic prophase and the G- and C-banding patterns and nucleolar organizer region (NOR) distribution were analyzed in Microtus kikuchii. M. kikuchii is closely related to M. oeconomus and M. montebelli, karyologically and systematically. The formation of a synaptonemal complex between the X and Y chromosomes at pachytene and end-to-end association at diakinesis – metaphase I are only observed in three species in the genus Microtus; M. kikuchii, M. oeconomus, and M. montebelli. All the other species that have been studied so far have had asynaptic X–Y chromosomes. These data confirm that M. kikuchii, M. oeconomus, and M. montebelli are very closely related, and support the separation of asynaptic and synaptic groups on the phylogenetic tree.Key words: Microtus kikuchii, Microtus phylogeny, karyotype, synaptic sex chromosomes, synaptonemal complex.


1999 ◽  
Vol 10 (4) ◽  
pp. 1235-1245 ◽  
Author(s):  
Manfred Alsheimer ◽  
Elisabeth von Glasenapp ◽  
Robert Hock ◽  
Ricardo Benavente

The nucleus of spermatocytes provides during the first meiotic prophase an interesting model for investigating relationships of the nuclear envelope (NE) with components of the nuclear interior. During the pachytene stage, meiotic chromosomes are synapsed via synaptonemal complexes (SCs) and attached through both ends to the nuclear periphery. This association is dynamic because chromosomes move during the process of synapsis and desynapsis that takes place during meiotic prophase. The NE of spermatocytes possesses some peculiarities (e.g., lower stability than in somatic cells, expression of short meiosis-specific lamin isoforms called C2 and B3) that could be critically involved in this process. For better understanding of the association of chromosomes with the nuclear periphery, in the present study we have investigated the distribution of NE proteins in relation to SC attachment sites. A major outcome was the finding that lamin C2 is distributed in the form of discontinuous domains at the NE of spermatocytes and that SC attachment sites are embedded in these domains. Lamin C2 appears to form part of larger structures as suggested by cell fractionation experiments. According to these results, we propose that the C2-containing domains represent local reinforcements of the NE that are involved in the proper attachment of SCs.


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.


1983 ◽  
Vol 61 (6) ◽  
pp. 1809-1814 ◽  
Author(s):  
Kathryn Carvey Crist ◽  
Donald R. Farrar

Solitary plants of Asplenium platyneuron occur disjunctively on recently produced coal spoils in southern Iowa. They are assumed to have been produced by self-fertilization of isolated gametophytes and therefore highly homozygous. Cultures of isolated and paired gametophytes originating from these solitary sporophytes produced second-generation sporophytes with 89 and 93% success, respectively, indicating a low genetic load as expected. The failure of gametophytes from coal-spoil plants to produce sporophytes with even greater success may result from homoeologous chromosome pairing and recombination at meiosis which allows production of variable spores and expression of genetic load from plants produced by self-fertilization of single gametophytes. Cultures of isolated and paired gametophytes originating from sporophytes in populations central to the species' range produced second-generation sporophytes with 83 and 90% success, respectively, indicating a significantly greater genetic load in populations but still a relatively low genetic load for the species. Through low genetic load, regularity of sporophyte production from isolated gametophytes, and ability of such plants to release variability through homoeologous chromosome pairing, Asplenium platyneuron is remarkably adapted for, and successful in, colonizing distant habitats through long-range spore dispersal.


1982 ◽  
Vol 58 (1) ◽  
pp. 411-422
Author(s):  
R. Benavente ◽  
R. Wettstein ◽  
M. Papa

An ultrastructural study was performed on the sex chromosomes (male X1X2X3O) during the spermatogenesis of Tegenaria domestica (Arachnida, Agelenidae). This study was carried out using random and serially cut sections. During pachytene and diplotene the three X chromosomes are longitudinally paired. Each of these consists of a central core of condensed chromatin, surrounded by a field of dense chromatin projections through which the chromosomes are in contact with one another. These projections may be responsible for the recognition and pairing of the sex chromosomes and in some way participate in their non-disjunction during anaphase I. A study of the structure and behaviour of the sex chromosomes during spermatogenesis is also presented. The available information on non-synaptonemal complex-mediated chromosome pairing and a systematization of sex chromosome structure in spiders are discussed.


Genome ◽  
1991 ◽  
Vol 34 (4) ◽  
pp. 553-560 ◽  
Author(s):  
C. A. Curtis ◽  
A. J. Lukaszewski ◽  
M. Chrzastek

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.


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