Synaptonemal complex behavior in asynaptic maize

Genome ◽  
1991 ◽  
Vol 34 (1) ◽  
pp. 163-168 ◽  
Author(s):  
Marjorie P. Maguire ◽  
Robert W. Riess
Keyword(s):  
Synaptonemal Complex ◽  
Chromosome Pairing ◽  
Early Stage ◽  
Complex Behavior ◽  
Synaptic Process ◽  
Polar Orientation

Synatonemal complexes were studied in silver-stained spread preparations of microsporocyte complements of asynaptic maize. Complexes were found predominantly in terminal regions of chromosome pairs. These tend to be aggregated in a common portion of the nucleus and to have polar orientation. As many as 19 of the 20 ends were found to be involved in relatively short paired segments. Intercalary regions of cores were not strongly organized and aligned, but some contained completed synaptonemal complex segments. The defect in asynaptic appears to represent stalling of the synaptic process at an early stage of synaptic progression.Key words: chromosome pairing, synaptonemal complex, synaptic defect.

Pattern of X-Y chromosome pairing in the Taiwan vole, Microtus kikuchii

Genome ◽  
2001 ◽  
Vol 44 (1) ◽  
pp. 27-31 ◽  
Author(s):  
K Mekada ◽  
M Harada ◽  
L K Lin ◽  
K Koyasu ◽  
P M Borodin ◽  
...  
Keyword(s):  
Synaptonemal Complex ◽  
Chromosome Pairing ◽  
Sex Chromosomes ◽  
Meiotic Prophase ◽  
Organizer Region ◽  
Nucleolar Organizer Region ◽  
Nucleolar Organizer ◽  
The Other ◽  
Banding Patterns ◽  
Y Chromosomes

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.

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.

scholarly journals Synaptonemal complex protein 3 as a novel prognostic marker in early stage non–small cell lung cancer

2013 ◽  
Vol 44 (4) ◽  
pp. 472-479 ◽  
Author(s):  
Joon-Yong Chung ◽  
Haruhisa Kitano ◽  
Mikiko Takikita ◽  
Hanbyoul Cho ◽  
Kyung Hee Noh ◽  
...  
Keyword(s):  
Lung Cancer ◽  
Small Cell Lung Cancer ◽  
Synaptonemal Complex ◽  
Prognostic Marker ◽  
Cell Lung Cancer ◽  
Early Stage ◽  
Small Cell ◽  
Small Cell Lung ◽  
Complex Protein ◽  
Synaptonemal Complex Protein

scholarly journals Human meiosis VIII. Chromosome pairing and formation of the synaptonemal complex in oocytes

1983 ◽  
Vol 48 (4) ◽  
pp. 457-483 ◽  
Author(s):  
Maja Bojko
Keyword(s):  
Synaptonemal Complex ◽  
Chromosome Pairing

Ultrastructural analysis of the X1X2X3O sex chromosome system during the spermatogenesis of Tegenaria domestica (Arachnida)

1982 ◽  
Vol 58 (1) ◽  
pp. 411-422
Author(s):  
R. Benavente ◽  
R. Wettstein ◽  
M. Papa
Keyword(s):  
Synaptonemal Complex ◽  
Chromosome Pairing ◽  
Sex Chromosomes ◽  
Ultrastructural Study ◽  
Chromosome Structure ◽  
Sex Chromosome ◽  
X Chromosomes ◽  
Sex Chromosome System ◽  
Available Information ◽  
Dense Chromatin

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.

Synaptonemal complex analysis of hybrid cattle. III. Meiotic pairing mechanisms in F1 Brahman × Hereford hybrids

Genome ◽  
1991 ◽  
Vol 34 (2) ◽  
pp. 228-235 ◽  
Author(s):  
A. E. Dollin ◽  
J. D. Murray ◽  
C. B. Gillies
Keyword(s):  
Synaptonemal Complex ◽  
Chromosome Pairing ◽  
Complex Analysis ◽  
Bos Taurus ◽  
Bos Indicus ◽  
Meiotic Pairing ◽  
Homoeologous Chromosome ◽  
Homoeologous Chromosome Pairing ◽  
Synaptonemal Complex Analysis ◽  
Complex Hybrid

The mechanisms of homoeologous chromosome pairing were studied in synaptonemal complex (SC) spreads of F1 Brahman (Bos indicus) × Hereford (Bos taurus) cattle. The most common SC abnormalities were bivalents with partial pairing failure and interlocks. While C-band polymorphisms could underlie most of the SC abnormalities observed in the full-blood cattle, other causes seem also to be contributing in the hybrids. The pattern of the abnormalities indicates that genie differences between the species were probably involved. Pachytene substaging data suggest that in some spreads, early pachytene bivalents with partial pairing failure may achieve complete synapsis or may be converted to interlocks by late pachytene.Key words: synaptonemal complex, hybrid cattle, interlocks.

Pattern of X–Y chromosome pairing in the Japanese field vole, Microtus montebelli

Genome ◽  
1997 ◽  
Vol 40 (6) ◽  
pp. 829-833 ◽  
Author(s):  
P. M. Borodin ◽  
M. B. Rogatcheva ◽  
K. Koyasu ◽  
K. Fukuta ◽  
K. Mekada ◽  
...  
Keyword(s):  
Synaptonemal Complex ◽  
Chromosome Pairing ◽  
Sex Chromosomes ◽  
Sex Chromosome ◽  
Chromosomal Evolution ◽  
The Other ◽  
Field Vole ◽  
Y Chromosomes ◽  
The One ◽  
Ancestral Type

Pairing of X and Y chromosomes at meiotic prophase in males of Microtus montebelli was analyzed. The sex chromosomes form a synaptonemal complex at pachytene and end-to-end association at diakinesis – metaphase I in two species of the genus Microtus (M. montebelli and M. oeconomus) only, while they do not pair at all in the other species of this genus that have been studied so far. These data confirm that M. montebelli and M. oeconomus are very closely related in their origin. It is suggested that the sex chromosomes of M. montebelli and M. oeconomus display the ancestral type of X–Y pairing. The lack of X–Y pairing in most species of Microtus appeared after the split in lineage that led to M. oeconomus and M. montebelli on the one hand and the remaining species on the other.Key words: Microtus montebelli, arvicoline phylogeny, synaptic sex chromosome, synaptonemal complex, chromosomal evolution.

Chiasma redistribution in the presence of different sized supernumerary segments in a grasshopper: dependence on nonhomologous synapsis

Genome ◽  
1997 ◽  
Vol 40 (5) ◽  
pp. 682-688 ◽  
Author(s):  
A. L. del Cerro ◽  
J. L. Santos
Keyword(s):  
Synaptonemal Complex ◽  
Synaptonemal Complexes ◽  
Chiasma Distribution ◽  
Length Measurements ◽  
Extra Segment ◽  
Synaptic Process ◽  
Nonhomologous Synapsis

Eight different sized supernumerary segments located at distal ends of the long arms of chromosomes M4, M5, M6, and S8 of the grasshopper Stenobothrus festivus were studied in males with regard to the synaptic process and chiasma distribution in the bivalents that carry them. The M4, M5, and M6 bivalents heterozygous for extra segments were always monochiasmate, in contrast to their bichiasmate condition observed in basic homozygotes. Furthermore, the presence of any of these extra segments led to chiasma redistribution in the carrier bivalents, so that such chiasmata were formed preferentially further away from the extra segment. The intensity of this effect is dependent on the size of the segment. Not all heteromorphic bivalents exhibited synaptonemal complexes with equalized axes at pachytene, but there was always a variable proportion of heterosynapsis around the distal ends of the long arms that was dependent on both the size of the segment and the size of the carrier chromosome. It is proposed that the absence of chiasmata in nonhomologous synapsed regions is responsible for the results obtained. Length measurements of the different extra segments and their carrier chromosomes between pachytene and diplotene indicated that synaptonemal complex is underrepresented in supernumerary heterochromatin.Key words: chiasma distribution, grasshopper, heterosynapsis, supernumerary segment, synaptonemal complex.

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.

The synaptonemal complex: does it have contractile proteins?

1984 ◽  
Vol 26 (6) ◽  
pp. 776-781 ◽  
Author(s):  
B. Spyropoulos ◽  
P. B. Moens
Keyword(s):  
Cell Motility ◽  
Synaptonemal Complex ◽  
Chromosome Pairing ◽  
Meiotic Prophase ◽  
Contractile Proteins ◽  
Experimental Approaches

Actin and myosin are commonly involved in cell motility systems. This study attempts to identify these two proteins in the synaptonemal complex (SC), a nuclear organelle associated with chromosome pairing during meiotic prophase. The several experimental approaches reported here give no evidence of SC staining with either anti-myosin or anti-actin antibodies. These findings differ from those of other reportings.Key words: synaptonemal complex, immunohistochemistry, contractile proteins, myosin, actin.

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