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  • 1
    ISSN: 1432-0886
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Medicine
    Notes: Abstract The ultrastructural distribution of small nuclear ribonucleoproteins (U1-snRNP and Sm antigen) in the nucleus ofChironomus salivary gland cells was investigated by means of specific antibodies and immunocytochemistry using colloidal gold complexes as markers. Particular attention was paid to the structural relationships of snRNPs with transcriptionally active areas in polytene chromosomes and with Balbiani ring granules. Our results demonstrate strong binding of anti-snRNP antibodies to RNP fibrils or the fibrillar network occurring within nuclear regions active in transcription (Balbiani rings or minor puffs). This confirms data reported previously on mammalian cells showing early association of snRNPs with nuclear fibrillar constituents containing newly synthesized pre-mRNA. In addition, Balbiani ring granules in the process of formation at the transcriptionally active sites were sometimes labeled on their periphery or on the transitory part between the granule and its precursor RNP fibril, while free granules observed in the nucleoplasm were virtually devoid of label. These findings suggest that mRNA processing, including splicing, takes place prior to the formation of mature Balbiani ring granules.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Springer
    Molecular biology reports 12 (1987), S. 180-181 
    ISSN: 1573-4978
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Summary: Possible snRNP states The data available at present suggest at least the following distinct states: a. free snRNP--possibly representing the active pool of recycling snRNP; b. loose snRNP:hnRNP complexes--these may represent snRNP involved in a “surveying” state prior to specific sequence interaction with pre-mRNA sites and perhaps characteristic of all polymerase II transcription sites; c. tight snRNP:hnRNP complexes--representing preformed spliceosome structures at specific sequence sites on pre-mRNA; d. ICG associated snRNP--function unknown, though possibly a storage structure of transiently inactive complexes.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Molecular Reproduction and Development 29 (1991), S. 209-219 
    ISSN: 1040-452X
    Keywords: snRNPs ; Nucleologenesis ; Transcription ; Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology
    Notes: Small nuclear ribonucleoproteins (snRNPs) were localized using human autoimmune or monoclonal anti-snRNP antibodies and ultrastructural immunocytochemistry in early preimplantation bovine embryos before and at transcription onset. Bovine cleavage stages up to 16-cell embryos were obtained either by culture of in vitro-fertilized ovarian oocytes or by isolation at slaughter of embryos fertilized and developed in vivo. Before transcription onset, up to the four-cell stage, diffuse labeling of nucleoplasm was detected, whereas cytoplasm labeling remained low. At the transcription onset, labeling of all eight-cell embryo nuclei was markedly concentrated at the borderline of already formed, condensed chromatin aggregates, where it was associated mainly with perichromatin fibrils. The condensed chromatin blocks revealed by several different staining methods were more prominent than is the case in most somatic cells. The degree of chromatin condensation and the pattern of its distribution differed between in vivo- and in vitro-produced eight-cell embryos: the in vitro embryos showed a higher degree of chromatin condensation and a peripheral distribution of chromatin blocks. A relation of this observation to the developmental potential of cow embryos is suggested. In two- and four-cell embryos, intensive labeling was seen in interchromatin granules, which, in their turn, were often seen in close proximity to the nucleous precursor bodies, or in the four-cell stage were interconnected to them. No labeling was ever seen, using antibodies specific for the snRNP Sm antigen, in nucleolar precursor bodies during embryonic nucleologenesis nor in the resulting nucleoli. There was some incidental labeling of the large central vacuole appearing at the beginning of the nucleolus precursor body transformation, testifying the nucleoplasmic origin of this entity.
    Additional Material: 11 Ill.
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Molecular Reproduction and Development 26 (1990), S. 150-158 
    ISSN: 1040-452X
    Keywords: hnRNP ; snRNP ; Ribosomal proteins ; DNA ; Ultrastructural cytochemistry ; Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology
    Notes: The chromatoid body (CB), a cytoplasmic organelle present only in germ cell line, was studied at the electron microscopic level in mouse spermatids using cytochemical techniques and specific antibodies directed against sn-RNPs, hnRNPs, and ribosomal proteins. We found that specific staining for DNA as well as the use of monoclonal anti-DNA antibodies show a complete absence of DNA in the CB. The CB remains stained, however, after the application of the ethidium bromide-PTA technique, suggesting the presence of RNA within this organelle. snRNP as well as hnRNP proteins are demonstrated within the CB by means of specific monoclonal or polyclonal antibodies, especially during earlier spermiogenic stages. Monoclonal antibodies directed against the large ribosomal subunit proteins P1/P2 detect these antigens on the CB essentially along the internal threads of dense fibrillar material. Our findings suggest that the CB may function as a source of mRNA and/or of its partially processed precursors during the late stages of spermiogenesis, when the spermatid nucleus becomes gradually inactive.
    Additional Material: 9 Ill.
    Type of Medium: Electronic Resource
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