TY - JOUR A1 - Bernards, R. A1 - Schackleford, G. M. A1 - Gerber, M. R. A1 - Horowitz, J. M. A1 - Friend, S. H. A1 - Schartl, Manfred A1 - Bogenmann, E. A1 - Rapaport, J. M. A1 - Mcgee, T. A1 - Dryja, T. P. T1 - Structure and expression of the murine retinoblastoma gene and characterization of its encoded protein N2 - No abstract available KW - Physiologische Chemie Y1 - 1989 U6 - http://nbn-resolving.de/urn/resolver.pl?urn:nbn:de:bvb:20-opus-61819 ER - TY - JOUR A1 - Benavente, Ricardo A1 - Scheer, Ulrich A1 - Chaly, Nathalie T1 - Nucleocytoplasmic sorting of macromolecules following mitosis: fate of nuclear constituents after inhibition of pore complex function N2 - PtK2 cells in which pore complex-mediated transport is blocked by microinjection early in mitosis of a monoclonal antibody (specific for an Mr 68000 pore complex glycoprotein) or of wheat germ agglutinin (WGA) complete cytokinesis. However, their nuclei remain stably arrested in a telophase-like organization characterized by highly condensed chromatin and the absence of nucleoli, indicating a requirement for pore-mediated transport for the reassembly of interphase nuclei. We have now examined this requirement more closely by monitoring the behavior of individual nuclear macromolecules in microinjected cells using immunofluorescence microscopy and have investigated the effect of microinjecting the antibody or WGA on cellular ultrastructure. The absence of nuclear transport did not affect the sequestration into daughter nuclei of components such as DNA, DNA topoisomerase I and the nucleolar protein fibrillarin that are carried through mitosis on chromosomes. On the other hand, lamins, snRNAs and the p68 pore complex glycoprotein, all cytoplasmic during mitosis, remained largely cytoplasmic in the telophase-arrested cells. Electron microscopy showed the nuclei to be surrounded by a doublelayered membrane with some inserted pore complexes. In addition, however, a variety of membranous structures with associated pore complexes was regularly noted in the cytoplasm, suggesting that chromatin may not be essential for the postmitotic formation of pore complexes. We propose that cellular compartmentalization at telophase is a two-step process. First, a nuclear envelope tightly encloses the condensed chromosomes, excluding non-selectively all macromolecules not associated with the chromosomes. Interphase nuclear organization is then progressively restored by selective pore complex-mediated uptake of nuclear proteins from the cytoplasm. KW - Cytologie KW - Nucleocytoplasmic transport KW - nuclear organization KW - nuclear envelope KW - nucleologenesis KW - mitosis Y1 - 1989 U6 - http://nbn-resolving.de/urn/resolver.pl?urn:nbn:de:bvb:20-opus-40777 ER - TY - JOUR A1 - Benavente, Ricardo A1 - Dabauvalle, Marie-Christine A1 - Scheer, Ulrich A1 - Chaly, Nathalie T1 - Functional role of newly formed pore complexes in postmitotic nuclear reorganization N2 - Many nuclear proteins are released into the cytoplasm at prometaphase and are transported back into the daughter nuclei at the end of mitosis. To determine the role of this reentry in nuclear remodelling during early interphase, we experimentally manipulated nuclear protein uptake in dividing cells. Recently we and others have shown that signal-dependent, pore complex-mediated uptake of nuclear protein is blocked in living cells on microinjection of the lectin wheat germ agglutinin (WGA), or of antibodies such as PI1 that are directed against WGA-binding pore complex glycoproteins. In the present study, we microinjected mitotic PtKz cells with WGA or antibody PIt and followed nuclear reorganization of the daughter cells by immunofluorescence and electron microscopy. The inhibitory effect on nuclear protein uptake was monitored by co-injection of the karyophilic protein nucleoplasmin. When injected by itself early in mitosis, nucleoplasmin became sequestered into the daughter nuclei as they entered telophase. In contrast, nucleoplasmin was excluded from the daughter nuclei in the presence of WGA or antibody PI1 . Although PtKz cells with blocked nuclear protein uptake completed cytokinesis, their nuclei showed a telophaselike organization characterized by highly condensed chromatin surrounded by a nuclear envelope containing a few pore complexes. These findings suggest that pore complexes become functional as early as telophase, in close coincidence with nuclear envelope reformation. They further indicate that the extensive structural rearrangement of the nucleus during the telophase-G1 transition is dependent on the influx of karyophilic proteins from the cytoplasm through the pore complexes, and is not due solely to chromosome- associated components. Y1 - 1989 U6 - http://nbn-resolving.de/urn/resolver.pl?urn:nbn:de:bvb:20-opus-40754 ER - TY - JOUR A1 - Baumhauer, Roland A1 - Busche, Detlef A1 - Sponholz, Barbara T1 - Reliefgeschichte und Paläoklima des saharischen Ost-Niger N2 - Der größte Teil des zentralsaharischen Reliefs ist unter dem Einfluß nicht-arider Klimate gebildet worden. Andererseits gab es im Pleistozän äolisch geprägte aride Phasen, die extremer als heutige gewesen sind. Der Kenntnisstand zur Reliefgeschichte erlaubt es, daraus die Grundzüge der Klimageschichte eines großen Teils der südlich-zentralen Sahara abzuleiten. KW - Geographie KW - Reliefgeschichte KW - Paläoklima KW - Ostniger Y1 - 1989 U6 - http://nbn-resolving.de/urn/resolver.pl?urn:nbn:de:bvb:20-opus-55378 ER - TY - JOUR A1 - Bach, Ulrich T1 - Oral rhetoric in writings for a mixed literate and illiterate audience N2 - No abstract available Y1 - 1989 U6 - http://nbn-resolving.de/urn/resolver.pl?urn:nbn:de:bvb:20-opus-47124 ER - TY - JOUR A1 - Alldrick, A. J. A1 - Lutz, Werner K. T1 - Covalent binding of [2-\(^{14}\)C]2-amino-3,8-dimethylimidazo[4,5-f]-quinoxaline (MeIQx) to mouse DNA in vivo N2 - Fernale BALB/c mice were administered intragastrically with equimolar amounts of either [2-\(^{14}\)C]2-amino-3,8-dimethyi[ 4,5-J]qulnoxaline (MeiQx) or 2-acetylamino[9-\(^{14}\)C]fluorene (2AAF). DNA was isolated from tissues of mice killed either 6 or 24 h after administration. Analysis of liver DNA nucleotide digests by HPLC analysis revealed that all of the radioactivity was attributable to adduct formation. Tbe specific activities of DNA samples were converted to covalent bindlog indices (CBI, J.LIDOI adduct per mol DNA nucleotides/mmol chemical app6ed per kg animal body weight). CBI values of 25 and 9 were detennined for 2AAF and MeiQx in tbe llvers of mice killed 6 h after dosing. The values were in general agreement with the moderate carcinogenic potency of these compounds. The specific activities of DNA preparations obtained from the lddneys, spleens, stomachs, small intestines and large intestlnes of mice treated witb MeiQx and killed 6 h after doslng were S- to 35-times less tban those obtained witb the llver. DNA isolated from tbe lungs (a target organ for MeiQx tumorigenicity) of MeiQx-treated mice was not radiolabeUed at tbe limit of detection (CBI <0.3). With tbe exception of tbe gastrolntestinal tract, the specific activities of DNA samples isolated from mice killed 6 h after administration were higher than those from mice killed after 24 h. KW - Toxikologie Y1 - 1989 U6 - http://nbn-resolving.de/urn/resolver.pl?urn:nbn:de:bvb:20-opus-60832 ER - TY - GEN T1 - Jahresbericht 1988 T1 - Annual Report 1988 N2 - Die Entwicklung der Universitätsbibliothek Würzburg im Jahr 1988. N2 - Annual Report of the University Library of Würzburg, 1988. T3 - Jahresbericht der Universitätsbibliothek Würzburg - 1988 KW - Würzburg KW - Universitätsbibliothek KW - Bericht KW - Jahresbericht KW - Würzburg KW - University Library KW - Report KW - Annual Report KW - Wuerzburg KW - Wurzburg Y1 - 1989 U6 - http://nbn-resolving.de/urn/resolver.pl?urn:nbn:de:bvb:20-opus-42329 ER -