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  • 1995-1999  (4)
  • 1975-1979
  • meiosis  (3)
  • Appressorium  (1)
  • 1
    Electronic Resource
    Electronic Resource
    Springer
    Chromosome research 4 (1996), S. 507-516 
    ISSN: 1573-6849
    Keywords: Arbidopsis ; cytogenetics ; light microscopy ; meiosis ; chromosomes
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract An atlas of meiosis inArabidopsis thaliana, encompassing all stages from preleptotene to telophase II and early microspore formation, is presented in detail for the first time. The photomicrographs and descriptions are based on staining with the DNA fluorochrome 4′,6-diamidino-2-phenylindole (DAPI) combined with a spreading procedure, or haematoxylin-iron alum (HIA) staining. Despite previous reservations about the practicality of cytogenetic meiotic analysis inArabidopsis due to its small genome size, good-quality and clearly analysable preparations of all meiotic stages were obtained. This atlas of normal, wild-type meiosis is considered an essential prerequisite to informed analyses of meiotic mutants. Furthermore, extended prophase I chromosomes, particularly at the pachytene stage, offer considerable potential for producing a detailed cytogenetic map (karyotype) ofArabidopsis chromosomes with the additional prospect of high-resolution physical mapping based on fluorescencein situ hybridization (FISH) of defined DNA probes to these extended chromosomes.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Springer
    Chromosome research 3 (1995), S. 433-439 
    ISSN: 1573-6849
    Keywords: allium porrum ; meiosis ; polyploid ; synaptonemal complex
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract Meiotic chromosome pairing of the tetraploid speciesAllium porrum, the cultivated leek, was analysed by electron microscopy of 83 surface-spread nuclei in the late zygotene to early diplotene interval of prophase I, from four different varieties. Prophase I quadrivalent frequency, at 71%, marginally but significantly exceeds the two-thirds expected on a simple random end-pairing model, suggesting that more than two autonomous pairing sites occur, in some tetrasomes at least. This pattern of synaptic behaviour is consistent with an autotetraploid status, but comparison with other tetraploids, including otherAllium species, indicates thatAllium porrum may be a weak segmental allopolyploid displaying limited preferential homologous pairing. The incidence of pairing partner switches (PPSs) in prophase I quadrivalents is relatively low; 90% of all analysed quadrivalents had only one or two PPSs. The positional distribution of PPSs along quadrivalents was distinctly uneven with peaks in mid-chromosome arms and reduced frequencies around centromeres and near the ends. The four different varieties of leek analysed were remarkably similar in their meiotic behaviour despite their diverse breeding history, but individual plants within varieties displayed substantial variation in quadrivalent and PPS frequencies.
    Type of Medium: Electronic Resource
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  • 3
    ISSN: 1573-6849
    Keywords: Arabidopsis ; fertility ; meiosis ; mutants ; T-DNA
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract A secondary screen of the Feldmann collection of T-DNA transformed Arabidopsis lines identified several meiotic mutants. We used a spreading technique combined with DAPI staining in a detailed cytogenetic analysis of meiotic chromosome behaviour in four of these mutants, all of which are putatively T-DNA tagged and therefore candidates for molecular and functional analysis of the mutated genes. Two of them are defined as ‘synaptic’ mutants, showing greatly reduced association of homologous chromosomes at metaphase I: one is asynaptic, showing failure of synapsis during prophase I, whereas the other is desynaptic and is characterized by normal but non-maintained synapsis. Another mutant is defective in meiotic cell cycle control and undergoes a third meiotic division, resembling a second division but without an additional round of chromosome duplication. A further mutant shows meiosis-limited chromosome disruption, resulting in extensive chromosome fragmentation combined with other defects. All four mutants experience very irregular chromosome distribution during the meiotic divisions, resulting in abnormal numbers and/or sizes of microspores, with resulting reduced fertility.
    Type of Medium: Electronic Resource
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  • 4
    ISSN: 1615-6102
    Keywords: Appressorium ; Colletotrichum ; Conidia ; Extracellular matrix ; Extracellular glycoproteins ; Monoclonal antibody
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Summary The ultrastructure and composition of the extracellular matrices (ECMs) associated with germ tubes and appressoria ofColletotrichum lindemuthianum have been examined. Flexuous fibres (fimbriae), up to 6 μm long and 4–30 nm in diameter, protruded from the surface of germ tubes and appressoria. Anionic colloidal gold and lectin cytochemistry showed that ECMs of germ tubes and appressoria contain basic proteins, α-D-mannose and α-D-galactose residues. A monoclonal antibody, UB26, was raised to infection structures isolated from leaves ofPhaseolus vulgaris infected withC. lindemuthianum. UB26 recognised a protein epitope on two glycoproteins (Mr 133,000 and 146,000). Reductions in the Mr of these proteins after treatment with peptide-N-glycosidase and trifluoromethane sulphonic acid suggest that they carry N- and O-linked side-chains. Immunofluorescence and EM-immunogold labelling showed that glycoproteins recognised by UB26 were restricted to the ECMs around germ tubes and appressoria but fimbriae were not labelled. Unlike appressorial germ tubes formed in vitro, intracellular infection hyphae were not labelled, suggesting that the glycoproteins recognised by UB26 are not present on fungal structures formed within host cells. In liquid culture, these glycoproteins were not released into the medium, suggesting they are physically linked to the cell wall. Also, the glycoproteins were not removed from glass surfaces by ultrasonication. These results suggest that glycoproteins recognised by UB26 may be involved in the adhesion of germ tubes and appressoria to substrata. Our results show that the ECMs of germ tubes and appressoria differ markedly in structure and composition from those of conidia and intracellular hyphae, and that extracellular glycoproteins are associated with specific regions of the fungal cell surface.
    Type of Medium: Electronic Resource
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