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1.
A method of in silico search for specific repetitive DNA sequences related to the synaptonemal complex (meiDNA) in mammalian genomes was developed. A study of the distribution of these repeats over chromosomes revealed their scarcity on the Y chromosome and a decrease in recombination frequency in regions enriched in meiDNA. The results are discussed in context of the model of the looplike meiotic chromosome organization during the formation of the synaptonemal complex. 相似文献
2.
Chromatin organization during meiotic prophase ofBombyx mori 总被引:1,自引:1,他引:0
Chromatin organization during the early stages of male meiotic prophase inBombyx mori was investigated by electron microscopy. The analysis of nuclei prepared by the Miller spreading procedure, suggests that chromatin fibers which are 200–300 Å in diameter undergo an orderly folding coincident with the formation of the synaptonemal complex. In very early stages the chromatin is released in linear arrays typical of interphase chromatin material. With time loops containing 5–25 of B conformation DNA, initially visualized at the periphery of early meiotic prophase nuclei, aggregate into discrete foci. These foci coalesce to form the longitudinal axis of the chromosome in conjunction with the initial appearance of the axial elements of the synaptonemal complex. At pachytene, the loops are evenly distributed along the length of the chromosome and extend radially so that in well spread preparations the chromosome has a brush-like appearance. Throughout this period nascent RNP-fibers were visualized along some of the loops. 相似文献
3.
Light and electron microscope studies of chromosome pairing in relation to chiasma localisation in Stethophyma grossum (Orthoptera: Acrididae) 总被引:1,自引:1,他引:0
G. H. Jones 《Chromosoma》1973,42(2):145-162
The relationship of chromosome pairing to chiasma localisation in the grasshopper Stethophyma grossum was investigated by a combined light and electron microscope study. Observations on the extent of synaptonemal complex formation in spermatocytes suggest that pairing is complete in all chromosome regions and that localised chiasmata do not therefore follow from localised pairing of homologues. This study also revealed an unprecedented variant of synaptonemal complex structure. Each bivalent was found to contain an asymmetrical region within which one lateral element was enormously enlarged while the other lateral element retained normal dimensions. This asymmetrical region is probably confined to one end of each bivalent and seems to extend constantly about 4 from the nuclear membrane attachment site. The possible significance of this variant of synaptonemal complex structure is briefly discussed. 相似文献
4.
Differentiation of the synaptonemal complex and the kinetochore in Locusta spermatocytes studied by whole mount electron microscopy 总被引:13,自引:2,他引:13
When Locusta migratoria spermatocytes are surface-spread on various salines, the axial element of leptotene and zygotene chromosomes, and the synaptonemal complex of pachytene chromosomes are well-preserved, although, in most instances, virtually denuded of chromatin. A complex association of chromosome ends with the nuclear membrane is apparent as early as leptotene, and, as pairing is initiated, the nuclear attachment points of the partner half-bivalents fuse, apparently incorporating additional membrane material between them. The meiotic kinetochore originates in association with the axial element during early prophase, and prior to synaptonemal complex formation and chromosome condensation. 相似文献
5.
The meiotic prophase in Bombyx mori females analyzed by three-dimensional reconstructions of synaptonemal complexes 总被引:3,自引:2,他引:1
Søren Wilken Rasmussen 《Chromosoma》1976,54(3):245-293
Serial sectioning followed by three dimensional reconstruction of lateral components of the synaptonemal complex have been used to follow chromosome pairing during the prophase of the achiasmatic meiotic division in the silkworm, Bombyx mori. During leptotene and early zygotene, the lateral components become attached to the nuclear envelope at a specific region, thus forming a chromosome bouquet. The attachment of lateral components to the nuclear envelope precedes the completion of the components between their attachment points. Synapsis and synaptonemal complex formation start during the period of lateral component organization in the individual nucleus. Telomeric movements on the nuclear envelope occur at two stages of the prophase: the chromosome pairing appears to be initiated by an association of unpaired ends of homologous chromosomes, the nature of this primary attraction and recognition being unknown. Secondly, the paired chromosomes become dispersed in the nucleus by shifting of attachment sites of completed synaptonemal complexes at the end of zygotene. This movement is possibly related to a membrane flow occurring during this stage. Membrane material is synthesized at the region of synaptonemal complex attachment. Later, the excess membrane material is shifted to the opposite pole where it protrudes into the lumen of the nuclei thus forming vacuoles. — Two previously undescribed features of chromosome pairing were revealed. In late zygotene, chromosome pairing and synaptonemal complex formation were frequently observed to be delayed or even prevented over a short distance by interlocking of two bivalents, both being attached to the nuclear envelope. Such interlocking of bivalents was not found in pachytene. Secondly, one nucleus was found in which two homologous chromosomes were totally unpaired while the remaining 27 bivalents were completed or in a progressed state of pairing. The lateral components of the two unpaired chromosomes had the same length and were located several microns apart, thus eliminating the possibility of a permanent association of homologous chromosomes before the onset of meiosis in Bombyx mori females. — During pachytene, one of the 8 cells belonging to the syncytial cell cluster characteristic of oogenesis continues the meiotic prophase whereas the remaining 7 cells, the nurse cells, enter a different developmental sequence, finally resulting in their degeneration. The synaptonemal complex of the oocyte develops into a sausage-like structure after pachytene by a deposition of dense material onto the lateral components, thus filling out most of the central region. The diameter of this modified synaptonemal complex reaches at least 300 nm, as compaired to a pachytene width of approximately 130 nm. Also, the length of synaptonemal complexes increases from 212 at zygotene/pachytene to at least 300 at the modified pachytene stage. In nurse cells, synaptonemal complexes are shed from the bivalents shortly after pachytene simultaneously with a condensation of the chromatin. These free synaptonemal complex fragments associate and form various aggregates, either more or less normal looking polycomplexes or various complex figures formed by reorganized synaptonemal complex subunits. Later stages have not been included in the present investigation. 相似文献
6.
L. D. Safronova F. N. Golenishchev E. V. Cherepanova M. I. Baskevich 《Russian Journal of Genetics》2011,47(7):857-863
The results of light and electron microscopic (EM) studies of meiosis in Microtus arvalis males of the karyoform “arvalis” (2n = 46, NFa = 80), in hybrids between the chromosomal forms arvalis and obscurus (2n = 46, NFa = 68), in M. rossiaemeridionalis voles (2n = 54, NFa = 54), and in a hybrid between the species M. rossiaemeridionalis and kermanensis (2n = 54, NFa = 54) are presented. SC (synaptonemal complex) karyotypes of the parental forms and the hybrids were constructed
on the basis of measurements of the length of autosomal SCs revealed by the EM analysis in spermatocytes at the stage of middle
pachytene. The SC karyotypes of M. arvalis and the hybrids ♀ obscurus × ♂ arvalis consist of 22 synaptonemal complexes of autosomal bivalents and the axial elements
of the synaptonemal complexes of the sex chromosomes X and Y. The SC karyotypes of M. rossiaemeridionalis and the hybrid M. rossiaemeridionalis × M. kermanensis consist of 26 synaptonemal complexes of autosomal bivalents and a sex bivalent; they differ only in the length of the Y chromosome
axis (Y chromosome in the hybrid was inherited from M. kermanensis). Asynaptic configurations of the autosomal SCs were not observed in the hybrids. The SC axial elements of the X and Y chromosomes
in the parental forms and in the hybrids were located close to each other throughout pachytene, but they did not form a synaptic
region. The normal synapsis in sterile hybrids (M. rossiaemeridionalis × M. kermanensis) and the behavior of the sex chromosomes in meiosis in fertile and sterile hybrids are discussed in the context of specific
features of meiosis and reproductive isolation. 相似文献
7.
C. B. Gillies 《Chromosoma》1973,43(2):145-176
Aldehyde fixation followed by staining with phosphotungstic acid produces differential contrast between the synaptonemal complex and the chromatin of maize pachytene bivalents. Centromeres, heterochromatic knobs and large chromomeres are easily recognised. With this and other staining techniques the nucleolus organizer region can be differentiated into two components. — Microsporocyte nuclei at pachytene were serially sectioned and all ten bivalents reconstructed in five nuclei. An idiogram was derived from the mean chromosome (= synaptonemal complex) lengths, the arm ratios, positions of knobs and the nucleolus organizer region. The idiogram agrees well with that published from light microscopic analyses. However, bivalent lengths are only two thirds of those observed by light microscopy of squash preparations. Many telomeres of the bivalents are connected via chromatin to the nuclear envelope, but a varying number of free bivalent ends are observed in all five reconstructed nuclei. — Bivalents heterozygous for inversion 3b were reconstructed. In the presence of abnormal chromosome 10 (K10) the lateral components of the synaptonemal complex of chromosome 3 formed a typical inversion loop, while in one of the nuclei having no K10 the two lateral components of the long arms of chromosome 3 remained unpaired in the region of inversion heterozygosity. The presence of K10, which increases crossing-over frequencies and promotes intimate pairing at the light microscopic level, was thus found to permit formation of complete synaptonemal complexes in the inverted region. The extra terminal portion of the K10 chromosome folded back on itself and formed a morphologically normal synaptonemal complex in this — possibly non-homologously paired — region. The chromatin of centromeres and knobs from different bivalents were sometimes found to fuse, but the synaptonemal complexes transversing the fused centromeres or knobs retained their individuality. 相似文献
8.
Scott A Boden Nadim Shadiac Elise J Tucker Peter Langridge Jason A Able 《BMC molecular biology》2007,8(1):65
Background
Pairing and synapsis of homologous chromosomes is required for normal chromosome segregation and the exchange of genetic material via recombination during meiosis. Synapsis is complete at pachytene following the formation of a tri-partite proteinaceous structure known as the synaptonemal complex (SC). In yeast, HOP1 is essential for formation of the SC, and localises along chromosome axes during prophase I. Homologues in Arabidopsis (AtASY1), Brassica (BoASY1) and rice (OsPAIR2) have been isolated through analysis of mutants that display decreased fertility due to severely reduced synapsis of homologous chromosomes. Analysis of these genes has indicated that they play a similar role to HOP1 in pairing and formation of the SC through localisation to axial/lateral elements of the SC. 相似文献9.
In organisms with chiasmatic meiosis two different relationships have been described between crossing over and synapsis: in
one group of organisms synapsis depends on the initiation of meiotic recombination while in the other group it is independent
of this initiation. These patterns have been observed mainly in organisms where all meiotic bivalents in the set have similar
behaviors. In some heteropteran insects a pair of chromosomes named m chromosomes is known to behave differently from autosomes
regarding synapsis and recombination. Here we used immunodetection of a synaptonemal complex component and acid-fixed squashes
to investigate the conduct of the small m chromosome pair during the male meiosis in the coreid bug Holhymenia rubiginosa. We found that the m chromosomes form a synaptonemal complex during pachytene, but they are not attached by a chiasma in
diakinesis. On the other hand, the autosomal bivalents synapse and recombine regularly. The co-existence of these variant
chromosome behaviors during meiosis I add further evidence to the absence of unique patterns regarding the interdependence
of synapsis and recombination. 相似文献
10.
Michael Klutstein Martin Xaver Ronen Shemesh Drora Zenvirth Franz Klein Giora Simchen 《Molecular genetics and genomics : MGG》2009,282(5):453-462
Synapsis of homologs during meiotic prophase I is associated with a protein complex built along the bivalents—the synaptonemal
complex (SC). Mutations in the SC-component gene ZIP1 diminish SC formation, leading to reduced recombination levels and low spore viability. Here we show that in SK1 strains
heterozygous for a deletion of ZIP1 in certain regions meiotic interference are impaired with no decrease in recombination levels. The extent of synapsis is
over all reduced and NDJ levels of a large endogenous chromosome and of artificial chromosomes (YACs) rise to twice the level
of wild type strains. A substantial proportion of mis-segregating YACs had undergone crossing over. This demonstrates that
different functions of Zip1 display differential sensitivities to changes in expression levels. 相似文献
11.
H Yang H R Jung S Solinas-Toldo E Lang R Bolt R Fries G Stranzinger 《Cytogenetics and cell genetics》1992,61(1):67-74
A reciprocal whole-arm translocation between chromosomes 1 and 6 in a Swiss Large White boar with reduced fertility was identified by the use of different staining techniques in mitotic metaphase cells, synaptonemal complex analyses, and meiotic chromosome preparations. The karyotype of this boar was demonstrated to be 38,XY,rcp(1;6)(1p6p;1q6q). To further localize the breakpoints more precisely and determine the precise gene locations, several in situ hybridization experiments were performed with a chromosome 1 centromere-specific probe and two other gene probes. The breakage and reunion points of both chromosomes were located in the centromeric regions. The genes for glucose phosphate isomerase and calcium release channel were mapped to 6cen----q12. 相似文献
12.
Ignacio Prieto Anna Kouznetsova Agnes Fütterer Varvara Trachana Esther Leonardo Astrid Alonso Guerrero Mercedes Cano Gamero Cristina Pacios-Bras Hervé Leh Malcolm Buckle Mónica Garcia-Gallo Leonor Kremer Antonio Serrano Fernando Roncal Juan Pablo Albar José Luis Barbero Carlos Martínez-A Karel H. M. van Wely 《Chromosoma》2009,118(5):617-632
Synapsis of homologous chromosomes is a key meiotic event, mediated by a large proteinaceous structure termed the synaptonemal
complex. Here, we describe a role in meiosis for the murine death-inducer obliterator (Dido) gene. The Dido gene codes for three proteins that recognize trimethylated histone H3 lysine 4 through their amino-terminal plant homeodomain
domain. DIDO3, the largest of the three isoforms, localizes to the central region of the synaptonemal complex in germ cells.
DIDO3 follows the distribution of the central region protein SYCP1 in Sycp3−/− spermatocytes, which lack the axial elements of the synaptonemal complex. This indicates that synapsis is a requirement
for DIDO3 incorporation. Interestingly, DIDO3 is missing from the synaptonemal complex in Atm mutant spermatocytes, which form synapses but show persistent trimethylation of histone H3 lysine 4. In order to further
address a role of epigenetic modifications in DIDO3 localization, we made a mutant of the Dido gene that produces a truncated DIDO3 protein. This truncated protein, which lacks the histone-binding domain, is incorporated
in the synaptonemal complex irrespective of histone trimethylation status. DIDO3 protein truncation in Dido mutant mice causes mild meiotic defects, visible as gaps in the synaptonemal complex, but allows for normal meiotic progression.
Our results indicate that histone H3 lysine 4 demethylation modulates DIDO3 localization in meiosis and suggest epigenetic
regulation of the synaptonemal complex. 相似文献
13.
Electron microscopic examination of gonads of Drosophila melanogaster with different genotypes, including a metafemale 3X;2A and an intersex XXY;3A have revealed that the formation of synaptonemal complexes is controlled by the genic balance, i.e., the ratio of X chromosomes to autosomes. The Y chromosome is not involved in the genetic control of the formation of precursors of the central element of synaptonemal complexes in males, nor does it disturb their formation in XXY females. Hyperploidy for sections 1-3A and 18A-20 of the X chromosome does not lead to the appearance of synaptonemal complexes in males and does not interfere with their formation in females. Females hyperploid for extensive regions of the X chromosome (sections 1-11A, 11A-20, and 8C-20) are fertile and show apparently normal formation of synaptonemal complexes. Hyperploidy for sections 8C-11A of the X results in a sharp decrease in the viability of females, in abnormal differentiation of ovary cells, and in the lack of synaptonemal complexes. These data suggest a possible important role for the sections 8C-11A in the genic balance controlling the formation of synaptonemal complexes in D. melanogaster. The lack of synaptonemal complexes in hypoploid females may be the result of abnormal cell differentiation in gonads. 相似文献
14.
Reconstruction of the Neurospora crassa pachytene karyotype from serial sections of synaptonemal complexes 总被引:3,自引:3,他引:0
C. B. Gillies 《Chromosoma》1972,36(2):119-130
Serial sections from isolated asci were used to reconstruct the seven pachytene bivalents of Neurospora crassa. The synaptonemal complex could be traced for its whole length in each bivalent, being attached to the nuclear envelope at both ends in six. The satellite end of the nucleolar chromosome did not appear to be attached to the nuclear envelope. The estimated lengths of the bivalents ranged from 10.7 to 5.1 microns in one nucleus, from 11.5 to 4.2 microns in another, and from 8.5 to 4.4 microns in a third, with total haploid complement lengths of 45.5 microns, 47.3 microns, and 43.9 microns respectively. These values are considerably smaller than published light microscopical measurements.—The synaptonemal complex in N. crassa, as in other ascomycetes, has two banded ca. 400 Å wide lateral components held about 1200 Å apart by a central region containing the ca. 200 Å wide central component. With normal glutaraldehyde/OsO4-phosphate buffered fixation the chromatin of the pachytene bivalents is poorly contrasted. Occasional local thickenings of the central component into electron dense nodes ca. 1000 × 500 Å in longitudinal section are characteristic of the complex. 相似文献
15.
S. V. Golubtsov S. P. Sosnikhina I. V. Iordanskaya A. V. Voilokov E. I. Mikhailova O. L. Kolomiets Yu. F. Bogdanov 《Russian Journal of Genetics》2010,46(6):682-688
A study was made of the expression and inheritance of the sy11 mutation, which alters homologous chromosome synapsis in meiotic prophase I of rye. The abnormal phenotype proved to be determined
by a recessive allele of a single sy11 gene. Univalents and multivalents were observed in homozygotes for the mutant allele. Analysis of the synaptonemal complex
revealed a combination of homologous and nonhomologous synapsis in the mutant. The nonhomologous synapsis frequency significantly
decreased in the course of meiotic prophase I in the mutant. The number of chiasmata per bivalent in metaphase I was 1.1 ±
0.01 versus 1.8 ± 0.01 in wild-type plants, and the number of univalents was 2.7 ± 0.06 versus 0.5 ± 0.05 in wild-type plants.
As a result, a broad range of abnormalities was observed at subsequent stages of meiosis and led to the formation of defective
microspores. Mutant plants were semisterile. 相似文献
16.
Identification of the Z-W bivalent in the silkworm,Bombyx mori 总被引:2,自引:0,他引:2
None of the 56 chromosomes including sex chromosomes have been identified in the silkworm so far, though the 28 linkage groups have been determined (Doira, 1986). The present study aims to demonstrate the sex chromosome bivalent in the oocyte by using a particular strain, the sex-limited yellow cocoon (Sy), in which a large fragment of the second chromosome was translocated onto the W chromosome. Among 28 bivalents in the oocyte of the Sy strain, an asymmetrical synaptonemal complex was observed, while in the oocyte of the control strains no such complex was found. We consider this complex as the Z-W bivalent in the silkworm. 相似文献
17.
G. E. Sulimova E. R. Rakhmanaliev E. A. Klimov A. A. Kompaniytsev I. G. Udina E. R. Zabarovsky L. L. Kisselev 《Molecular Biology》2005,39(4):593-607
Using nucleotide sequences from jumping and linking NotI libraries of human chromosome 3, 94 NotI-STS markers for 72 individual NotI clones were developed. The positions of the NotI-STS markers and their order on the chromosome were determined by a combination of RH-mapping (our data), contig mapping, cytogenetic mapping, and in silico mapping. Comparison of NotI-STS DNAs with human genome sequences revealed two gaps in the regions 3p21.33 (marker NL1-256) and 3p21.31 (NL3-005), and a segmental duplication. Identical DNA fragments were found in the regions 12q and 3p22–21.33 (marker NL3-007). In the 3q28–q29 region (marker NLM-084), a fragment was detected whose identical copies were also present on chromosomes 1, 2, 15, and 19. For 69 NotI-STSs, significant homologies to nucleotide sequences of 70 genes and 2 cDNAs were detected (with homologies in NotI-STS 5′- and 3′-terminal sequences being taken into account). An association between NotI-STSs and genes is confirmed by a strong correlation between the density distributions of genes and NotI-STS markers on the map of human chromosome 3. Our results indicate that the NotI map may be regarded as a gene map of human chromosome 3. Thus, NotI-STSs are applicable as gene markers.__________Translated from Molekulyarnaya Biologiya, Vol. 39, No. 4, 2005, pp. 687–701.Original Russian Text Copyright © 2005 by Sulimova, Rakhmanaliev, Klimov, Kompaniytsev, Udina, Zabarovsky, Kisselev. 相似文献
18.
长鬣蜥的染色体组型和减数分裂联会复合体的研究 总被引:2,自引:0,他引:2
本文报道长鬣蜥(Physignathus cocincinus)有丝分裂染色体及C-,Ag-带以及减数分裂联会复合体核型。染色体数2n=36,NF=48,核型组成为12V+24m(V为双臂大染色体,其中No.2为亚中着丝粒染色体,m为微小染色体)。结构异染色质主要分布在小染色体上。一对Ag-NORs分布于第2对亚中着丝粒染色体末端。 相似文献
19.
Sex chromosome pairing during male meiosis in marsupials 总被引:9,自引:0,他引:9
Peter Sharp 《Chromosoma》1982,86(1):27-47
The pairing of the sex chromosomes at pachytene has been examined in twenty-two species of Australian marsupials, including four with complex sex chromosome systems. The axial elements of the sex chromosomes associate in all but one species. However, no synaptonemal complex has been observed between the axes of the X and Y chromosome in any of the examined species. Both the type of association between the sex chromosome axes, and the structural modifications of these axes are conserved within taxonomic groupings. In three species with complex sex chromosome systems, the t(XA), Y, A trivalents do not have a favoured relative orientation of the axes of the Y and A chromosomes, whereas in a fourth species with a t(XA1), t(A2YA2), A2 system the t(XA1) and A2 axes are in a cis arrangement with each other. 相似文献
20.
Bruno Delobel Ratib Djlelati Odette Gabriel-Robez Marie-Françoise Croquette Roselyne Rousseaux-Prévost Jean Rousseaux Jean-Marc Rigot Y. Rumpler 《Human genetics》1998,102(1):98-102
An apparently balanced reciprocal translocation 46,X,t(Y;6) (q11.23 ∼ q12;p11.1) was observed in an infertile man with severe
oligozooteratozoospermia. Different mitotic chromosome banding patterns were performed and fluorescence in situ hybridization
indicated a breakpoint in the fluorescent Yq heterochromatin. Molecular genetic deletion experiments for the azoospermia factor
region in distal Yq11 showed the retention of the DAZ gene and meiotic pairing configurations suggested that the man’s infertility
could be due to the pairing behaviour of the Y;6 translocation chromosome with the X chromosome visualised by synaptonemal
complex analysis at the electron microscopy level. The morphological appearance of the normal chromosome 6 and the Y;6 translocated
chromosome included in the compartment of the sex vesicle may allow an explanation of the degeneration of most spermatocytes
after the pachytene stage.
Received: 1 August 1997 / Accepted: 25 September 1997 相似文献