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  • 1
    ISSN: 1432-0886
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Medicine
    Notes: Abstract. On the assumption that Rad51 protein plays a role in early meiotic chromosomal events, we examine the location and time of appearance of immuno-reactive Rad51 protein in meiotic prophase chromosomes. The Rad51 foci in mouse spermatocytes appear after the emergence of, and attached to, short chromosomal core segments that we visualize with Cor1-specific antibody. These foci increase in number to about 250 per nucleus at the time when core formation is extensive. The numbers are higher in mouse oocytes and lower in rat spermatocytes, possibly correlating with recombination rates in those cases. In the male mouse, foci decrease in number to approximately 100 while chromosome synapsis is in progress. When synapsis is completed, the numbers of autosomal foci decline to near 0 while the X chromosome retains about 15 foci throughout this time. This stage coincides with the appearance of testis-specific histone H1t at mid- to late pachytene. Electron microscopy reveals that at first Rad51 immunogold-labeled 100 nm nodules are associated with single cores, and that they come to lie between the chromosome cores during synapsis. It appears that these nodules may be the homologs of the Rad51-positive early nodules that are well documented in plants. The reciprocal recombination-correlated late nodules appear after the Rad51 foci are no longer detectable. The absence of Rad51 foci in the chromatin loops suggests that in wild-type mice Rad51/DNA filaments are restricted to DNA at the cores/synaptonemal complexes. The expected association of Rad51 protein with Rad52 could not be verified immunocytologically.
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  • 2
    ISSN: 1432-0886
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Medicine
    Notes: Abstract.  The ATR (ataxia telangiectasia- and RAD3-related) protein is present on meiotic prophase chromosome cores and paired cores (synaptonemal complexes, SCs). Its striking characteristic is that the protein forms dense aggregates on the cores and SCs of the last chromosomes to pair at the zygotene-pachytene transition. It would appear that the ATR protein either signals delays in pairing or it is directly involved in the completion of the pairing phase. Atm-deficient spermatocytes, which are defective in the chromosome pairing phase, accumulate large amounts of ATR. The behaviour of ATR at meiotic prophase sets it apart from the distribution of the RAD51/DMC1 recombinase complex and our electron microscope observations confirm that they do not co-localize. We failed to detect ATM in association with cores/SCs and we have reported elsewhere that RAD1 protein does not co-localize with DMC1 foci. The expectation that putative DNA-damage checkpoint proteins, ATR, ATM and RAD1, are associated with RAD51/DMC1 recombination sites where DNA breaks are expected to be present, is therefore not supported by our observations.
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  • 3
    Electronic Resource
    Electronic Resource
    Springer
    Chromosoma 15 (1964), S. 231-242 
    ISSN: 1432-0886
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Medicine
    Notes: Summary 1. Meiotic prophase in the tomato was studied through the use of longitudinal anther sections. The existence of a maturity gradient through each pollen sac was established and the proper sequence of meiotic prophase stages determined. 2. After pachynema the homologous arms separate; the centromeres, and frequently the telomeres, remain paired. The stage has traditionally been interpreted as zygonema occuring before pachynema. It is suggested that this stage be referred to as schizonema. 3. Progressive separation causes the nucleus to become filled with strands. The stage is referred to as diffuse stage. During diffuse stage the centromeres become separated. 4. The individual bivalents become discernible again as diplotene chromosomes, the centromeres are separated and the homologous arms are held together at points of contact. Diakinesis follows. 5. Normal pachynema, the stage during which the chromosomes spread easily and therefore preferred for cytological studies, is preceded, for a considerable length of time, by cells which have tightly-bunched pachytene (paired) chromosomes. These cells are preceded by very early pollen mother cells which have interphase nuclei. 6. Evidence is presented that the sequence interphase — pachynema — schizonema — diffuse stage — diplonema — diakinesis exists in some other plants as well. 7. It is suggested that synapsis is complete in interphase, prossibly prior to duplication. If a similarity exists to Neurospora meiotic prophase, it may be that the telophase chromosomes of the premeiotic mitosis synapse and then elongate.
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  • 4
    Electronic Resource
    Electronic Resource
    Springer
    Chromosoma 19 (1966), S. 277-285 
    ISSN: 1432-0886
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Medicine
    Notes: Abstract A technique is described which gives well-defined label on meiotic chromosomes which incorporated tritiated thymidine two or more mitotic cycles prior to meiosis. It is shown that the distribution of label on meiotic chromosomes can be used to determine in which mitotic cycles label was incorporated. It is concluded that sister chromatid exchanges are common prior to meiosis, and that chiasmata do not show crossing-over of labeled material as is expected if the chiasmata are the result of breakage and rejoining or if chiasmata and crossovers are not related.
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  • 5
    Electronic Resource
    Electronic Resource
    Springer
    Chromosoma 23 (1968), S. 418-451 
    ISSN: 1432-0886
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Medicine
    Notes: Abstract The development of meiotic prophase in pollen mother cells ofLilium longiflorum is presented through photomicrographs of squashes and sections and through electron micrographs of thick and thin sections. Emphasis is placed on the first appearance of axial cores, the participation of axial cores in the formation of synaptinemal complexes, the fine structure of the complex and the fate of the complex at the end of pachytene. It is shown that axial cores are formed in early meiotic prophase chromosomes and that the two axial cores of a set of homologous chromosomes participate in the formation of a synaptinemal complex. It is proposed that the transverse filaments of each axial core meet and interdigitate and so produce the transverse filaments of the complex. It is shown that the complex is axial to the pachytene bivalent and that the association of the complex with chromosomal material is terminated at the end of pachytene. The pairing affinity of the cores in homologous and non-homologous chromosome associations is discussed. The zygotene stage is defined in terms of the occurrence of synaptinemal complexes and the attachment of the nucleolus to the nuclear membrane during this stage is noted.
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  • 6
    Electronic Resource
    Electronic Resource
    Springer
    Chromosoma 28 (1969), S. 1-25 
    ISSN: 1432-0886
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Medicine
    Notes: Abstract At the leptotene stage of meiotic prophase in Locusta spermatocytes (2n=22 telocentric autosomes + X-chromosome), each chromosome forms an axial core. The 44 ends of the autosomal cores are all attached to the nuclear membrane in a small region opposite the two pairs of centrioles of the juxtanuclear mitochondrial mass. At later stages of meiotic prophase, the cores of homologous chromosomes synapse into synaptinemal complexes. Synapsis is initiated near the nuclear membrane, in the centromeric and the non-centromeric ends of the chromosomes. Homologous cores have their attachment points close together and some cores are co-aligned prior to synapsis. At subsequent stages of zygotene, the number of synaptinemal complexes at the membrane increases, while the number of unpaired axial cores diminishes. At pachytene, all 11 bivalents are attached to the membrane at both ends, so that there are 22 synaptinemal complexes at the membrane near the centrioles. Because each bivalent makes a complete loop, the configuration of the classic Bouquet stage is produced. The X-chromosome has a poorly defined single core at pachytene which also attaches to the nuclear membrane. These observations are based on consecutive serial sections (50 to 100) through the centriolar zone of the spermatocytes. Labeling experiments demonstrated that tritiated thymidine was incorporated in the chromatin of young spermatocytes prior to the formation of the axial cores at leptotene. It is concluded that premeiotic DNA synthesis is completed well in advance of pairing of homologous chromosomes, as marked by the formation of synaptinemal complexes.
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  • 7
    Electronic Resource
    Electronic Resource
    Springer
    Chromosoma 41 (1973), S. 37-62 
    ISSN: 1432-0886
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Medicine
    Notes: Abstract The nucleus of the maturing oocytes expands to a large thin body of 400×140×3 μm but the chromosomes remain together in a small sphere, 15 μm in diameter. In Aedes aegypti this sphere becomes surrounded by one to several layers of polycomplexes, annulated polycomplexes, and related annulated pseudomembranes. Just prior to egg laying the expanded nucleus disintegrates while the sphere of chromosomes is surrounded by several layers of membranes. In Culex pipiens the elements which normally connect the lateral elements of the synaptonemal complexes become extended so that all bivalents become interconnected by a framework of pseudomembranes. The continuity between the modified synaptonemal complexes and various membranes associated with the karyosphere suggest that a relationship exists, by origin or by specialization, between the synaptic structures and nuclear envelope.
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  • 8
    Electronic Resource
    Electronic Resource
    Springer
    Chromosoma 67 (1978), S. 41-54 
    ISSN: 1432-0886
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Medicine
    Notes: Abstract The pachytene karyotypes of three grasshopper species with 2 and 3 Robertsonian fusions were constructed from electron micrographs of serially sectioned spermatocyte nuclei. Tracings of the synaptonemal complexes permitted identification of each bivalent and its centromeric region. Chromosomes with the centromere in a terminal position have a knob of centric heterochromatin on the synaptonemal complex where it ends at the nuclear envelope. In Chorthippus and in Chloealtis the submetacentric Robertsonian fusion chromosomes each have a single centric knob in the appropriate place. In Neopodismopsis each of the 2 submetacentric chromosomes have a centric knob which is double in size and structure. In spermatogonial metaphases the submetacentric chromosomes of Neopodismopsis have 70–80 microtubules per kinetochore while the telocentric chromosomes have 30–40 tubules per kinetochore. These observations are correlated with evidence from light microscopy that Robertsonian fusions may produce mono- or dicentric chromosomes.
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  • 9
    Electronic Resource
    Electronic Resource
    Springer
    Chromosoma 61 (1977), S. 41-48 
    ISSN: 1432-0886
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Medicine
    Notes: Abstract Each microspore of the onion Allium fistulosum (n=8) has 8 chromosomes. It is shown that in the microspore the 8 centromeres aggregate to form 2 or 3 centromeric structures. Subsequently, at early mitotic prophase, these aggregates are resolved into 8 separate centromeres and each becomes structurally double. After mitosis the pollen grain contains 2 nuclei, each with 8 separate and distinct centromeres, clustered at the nuclear envelope. As interphase progresses the centromeres of the vegetative nucleus are no longer at the nuclear envelope and they aggregate into 3 or 4 centromeric masses. In the generative nucleus there is less movement. The interphase centromere movements occur in the absence of microtubules. The centromeres range in size from about 0.10 to 0.17 μm3 with an average of 0.14 μm3 per centromere.
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  • 10
    Electronic Resource
    Electronic Resource
    Springer
    Chromosoma 103 (1994), S. 401-407 
    ISSN: 1432-0886
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Medicine
    Notes: Abstract With simultaneous immunofluorescence and fluorescent in situ hybridization, we have determined the organization of native and heterologous DNA sequences relative to the cores of meiotic prophase chromosomes. The normal chromatin organization is demonstrated with probes of mouse sequences: a cosmid probe that identities unique sequences and a 720 kb yeast artificial chromosome (YAC) probe that recognizes a specific region of the chromatin domain. The heterologous DNA consists of a 1.8 Mb insertion of 40 tandem head-to-tail phage λ LIZ vectors and of 11.4 Mb of bacterial/mouse DNA repeats. The lengthy λ insert is unusual in that it is not contained in the chromatin domain of chromosome 4 and in that it fails to form direct attachments to the chromosome core. The ends are attached indirectly, probably by means of the flanking mouse sequences. At late stages of meiotic prophase, while the terminal attachments remain the same, the λ DNA becomes highly compacted. Apparently, higher order condensation and core attachment are independent processes. The condensed inserts relax precociously at metaphase I. In the mouse heterozygous for the insert, the two sister inserts are usually merged, as are all four inserts in the homozygous mouse. Evidently chromatin loops with identical sequences can become associated during meiotic prophase. Mouse sequences within a heterologous DNA insert (repeats of bacterial plasmid pBR322 with a mouse β-globin insert) were observed to restore some degree of core attachment.
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