TY  - JOUR
A1  - Barnekow, A.
A1  - Schartl, Manfred
A1  - Anders, F.
A1  - Bauer, H.
T1  - Identification of a fish protein associated with a kinase activity and related to the Rous sarcoma virus transforming protein
N2  - No abstract available
KW  - Physiologische Chemie
Y1  - 1982
U6  - http://nbn-resolving.de/urn/resolver.pl?urn:nbn:de:bvb:20-opus-61946
ER  - 
TY  - JOUR
A1  - Kreft, Jürgen
A1  - Hughes, Colin
T1  - Cloning vectors derived from plasmids and phage of Bacillus
N2  - No abstract available
Y1  - 1982
U6  - http://nbn-resolving.de/urn/resolver.pl?urn:nbn:de:bvb:20-opus-47014
ER  - 
TY  - CHAP
A1  - Scheer, Ulrich
A1  - Zentgraf, Hanswalter
T1  - Morphology of nucleolar chromatin in electron microscopic spread preparations
N2  - No abstract available
Y1  - 1982
U6  - http://nbn-resolving.de/urn/resolver.pl?urn:nbn:de:bvb:20-opus-41155
ER  - 
TY  - JOUR
A1  - Scheer, Ulrich
T1  - A novel type of chromatin organization in lampbrush chromosomes of Pleurodeles waltlii: visualization of clusters of tandemly repeated, very short transcriptional units
N2  - A novel chromatin configuration is described in lampbrush chromosomes of Pleurodeles waltlii oocytes which is different from transcriptionally inactive chromatin as weil as from the various forms of transcribed chromatin hitherto described. This novel type of chromatin is not arranged in Christmas tree-Iike configurations of densely packed lateral ribonucleoprotein (RNP) fibriIs but is characterized by a periodic alternating pattern of thick and thin regions which occur in clusters 01 some 10,000 repeats. Each thickened unit with an average length of 45 nm contains two c10sely spaced particles, the putative RNA polymerases, and each thickened unit is separated from the next one by a beaded chromatin spacer with a length of about 80 nm. This chromatin spacer contains on average two particles of approximately 14 nm in diameter, assumed to be nucleosomes. The thickened regions are interpreted to represent short transcriptional units containing approximately 130 base pairs of DNA which are separated from each other by nontranscribed spacers of 240-400 base pairs of DNA. The possibility is discussed that these transcriptional units represent 5S rRNA or tRNA genes.
KW  - Lampbrush chromosomes
KW  - Amphibian oocytes
KW  - Transcription units
KW  - Electron microscopy
Y1  - 1982
U6  - http://nbn-resolving.de/urn/resolver.pl?urn:nbn:de:bvb:20-opus-41087
ER  - 
TY  - JOUR
A1  - Sommerville, John
A1  - Scheer, Ulrich
T1  - Transcription of complementary repeat sequences in amphibian oocytes
N2  - Repeat sequences are transcribed in the germinal vesicles of amphibian oocytes. In the hnRNA population both complements of the repeats are found and can be readily detected because they form intermolecular duplex structures. The structure and formation of duplex regions have been studied in the hnRNA of Xenopus laevis, Triturus cristatus, Amphiuma means and Necturus maculosus, a series of amphibians of increasing genome size (C-value). In T. cristatus, the duplex structures are mostly 600- 1200 bp in length, whereas in X. laevis they are shorter and in N. maculosus they tend to be longer. Although the proportion of RNA sequence capable of rapidly forming duplex structures is different in different organisms, this property bears no relationship to C-value. However the sequence complexity of complementary repeats, as estimated from the rate of duplex formation, does show an increasing trend with C-value. The complementary repeats found in oocyte hnRNA are transcribed from families of DNA sequence that are each represented in the genome by thousands of copies. The extent of cross-species hybridization is low, indicating that the repeat sequences transcribed in different amphibian genera are not the same. In situ hybridization experiments indicate that the repeat sequences are spread throughout the genome. The evolution and possible function of complementary repeats are considered.
Y1  - 1982
U6  - http://nbn-resolving.de/urn/resolver.pl?urn:nbn:de:bvb:20-opus-33915
ER  - 
TY  - CHAP
A1  - Scheer, Ulrich
T1  - Electron microscopic analysis of chromatin and gene expression
N2  - No abstract available
Y1  - 1982
U6  - http://nbn-resolving.de/urn/resolver.pl?urn:nbn:de:bvb:20-opus-39456
ER  - 
TY  - JOUR
A1  - Scheer, Ulrich
A1  - Sommerville, John
T1  - Sizes of chromosome loops and hnRNA molecules in oocytes of amphibia of different genome sizes
N2  - The lengths of lampbrush chromosome loops and their tran scription units show a positive correlation with genome size in oocytes of amphibia with different C values. However, there is no such correlation with contour lengths of hnRNA molecu les isolated from these oocytes. These results indi cate th at more ON A sequences are transcribed in amphibia of higher C value , but that processing of RNA transc ripts occurs while they are still attached to the chromosomes as nascent ribonucleoprotein fibrils.
Y1  - 1982
U6  - http://nbn-resolving.de/urn/resolver.pl?urn:nbn:de:bvb:20-opus-33094
ER  - 
TY  - JOUR
A1  - Moreno-Diaz de la Espina, Susana
A1  - Franke, Werner W.
A1  - Krohne, Georg
A1  - Trendelenburg, Michael F.
A1  - Grund, Christine
A1  - Scheer, Ulrich
T1  - Medusoid fibril bodies: a novel type of nuclear filament of diameter 8 to 12 nm with periodic ultrastructure demonstrated in oocytes of Xenopus laevis
N2  - No abstract available
Y1  - 1982
U6  - http://nbn-resolving.de/urn/resolver.pl?urn:nbn:de:bvb:20-opus-34116
ER  - 
TY  - JOUR
A1  - Schartl, A.
A1  - Schartl, Manfred
A1  - Anders, F.
T1  - Promotion and regression of neoplasia by testosterone-promoted cell differentiation in Xiphophorus and Girardinus
N2  - No abstract available.
KW  - Schwertkärpfling
KW  - Lebendgebärende Zahnkarpfen
Y1  - 1982
U6  - http://nbn-resolving.de/urn/resolver.pl?urn:nbn:de:bvb:20-opus-86684
ER  - 
TY  - JOUR
A1  - Schartl, Manfred
A1  - Barnekow, Angelika
T1  - The expression in eukaryotes of a tyrosine kinase which is reactive with pp60v-src antibodies
N2  - All specimens of Eumetazoa and Parazoa, ranging from mammals, birds, teleosts, sharks, lampreys, amphioxus, insects, down to sponges showed the pp60c-src associated kinase activity, indicating that c-src, which is the cellular homologue of the oncogene v-src of Rous sarcoma virus (RSV) is probably present in all multicellular animals. Protozoa and plants did not show pp60c-src: kinase activity.
The degree of c-src expression depends on the taxonomic rank of the Eumetazoa tested, and is organ-specific with nervaus tissues displaying the highest kinase activities. In the central nervous system of mammals and birds we found a high c-src expression, and in that of the lampreys, amphioxus, and insects the lowest. Unexpectedly, total extracts of sponges showed an amount of pp60c-src kinase activity similar to that of brain cell extracts of mammals and birds. These findings suggest that pp60c-src is a phylogenetic old protein that might have evolved together with the multicellular organisation of Metazoa, and that might be of importance in proliferation and differentiation of nontransformed cells.
KW  - Protein-Tyrosin-Kinasen
KW  - Eukaryoten
Y1  - 1982
U6  - http://nbn-resolving.de/urn/resolver.pl?urn:nbn:de:bvb:20-opus-86208
ER  - 
TY  - CHAP
A1  - Scheer, Ulrich
A1  - Kleinschmidt, Jürgen A.
A1  - Franke, Werner W.
T1  - Transcriptional and skeletal elements in nucleoli of amphibian oocytes
N2  - No abstract available
Y1  - 1982
U6  - http://nbn-resolving.de/urn/resolver.pl?urn:nbn:de:bvb:20-opus-40625
ER  - 
TY  - JOUR
A1  - Hoppe, J.
A1  - Friedl, P.
A1  - Schairer, H. U.
A1  - Sebald, Walter
A1  - Meyenburg, K. von
A1  - Jorgensen, B. B.
T1  - The topology of the proton translocating F\(_0\) component of the ATP synthase from E. coli K12: studies with proteases
N2  - The accessibility of the three F\(_0\) subunits a, b and c from the Escherichia coli Kll A TP synthase to various proteases was studied in F\(_1\)-depleted inverted membrane vesicles. Subunit b was very sensitive to all applied proteases. Chymotrypsin produced a defined fragment of mol. wt. 1S 000 which remained tightly bound to the membrane. The cleavage site was located at the C-terminal region of subunit b. Larger amounts of proteases were necessary to attack subunit a (mol. wt. 30 000). There was no detectable deavage of subunit c. It is suggested that the major hydrophilic part of subunit b extends from the membrane into the cytoplasm and is in contact with the F\(_1\) sector. The F\(_1\) sector was found to afford some protection against proteolysis oftheb subunit in vitro andin vivo. Protease digestion bad no influence on the electro-impelled H\(^+\) conduction via F\(_0\) bot ATP-dependent H\(^+\) translocation could not be reconstituted upon binding of F\(_1\)• A possible role for subunit b as a linker between catalytic events on the F\(_1\) component and the proton pathway across the membrane is discussed.
KW  - Biochemie
KW  - protein pathway
KW  - ATPase mutants
Y1  - 1983
U6  - http://nbn-resolving.de/urn/resolver.pl?urn:nbn:de:bvb:20-opus-62718
ER  - 
TY  - JOUR
A1  - Kreft, Jürgen
A1  - Burger, Klaus J.
A1  - Goebel, Werner
T1  - Expression of antibiotic resistance genes from Escherichia coli in Bacillus subtilis
N2  - Bifunctional recombinant plasmids were constructed, comprised of the E. coli vectors pBR322, pBR325 and pACYC184 and different plasmids from Gram-positive bacteria, e.g. pBSU161-1 of B. subtilis and pUB110 and pC221 of S. aureus. The beta-lactamase (bla) gene and the chloramphenicol acetyltransferase (cat) gene from the E. coli plasmids were not transcribed and therefore not expressed in B. subtilis. However, tetracycline resistance from the E. coli plasmids was expressed in B. subtilis. Transcription of the tetracycline resistance gene(s) started in B. subtilis at or near the original E. coli promoter, the sequence of which is almost identical with the sequence recognized by σ<sup>55</sup> of B. subtilis RNA polymerase.
KW  - Biologie
Y1  - 1983
U6  - http://nbn-resolving.de/urn/resolver.pl?urn:nbn:de:bvb:20-opus-60600
ER  - 
TY  - JOUR
A1  - Kreft, Jürgen
A1  - Berger, Harald
A1  - Härtlein, Michael
A1  - Müller, Bodo
A1  - Weidinger, Gerhard
A1  - Goebel, Werner
T1  - Cloning and expression in Escherichia coli and Bacillus subtilis of the hemolysin (cereolysin) determinant from Bacillus cereus
N2  - From a cosmid gene bank of Bacillus cereus GP4 in Escherichia coli we isolated clones which, after several days of incubation, formed hemolysis zones on erythrocyte agar plates. These clones contained recombinant cosmids with B. cereus DNA insertions of varying lengths which shared some common restriction fragments. The smallest insertionwas recloned as aPstl fragment into pJKK3-1, a shuttle vector which repücates in Bacillus subtilis and E. coli. When this recombinant plasmid (pJKK3-1 hly-1) was transformed into E. coli, it caused hemolysis on erythrocyte agar plates, but in liquid assays no extemal or intemal hemolytic activity could be detected with the E. coli transformants. B. subtilis carrying the same plasmid exhibited hemolytic activity at Ievels comparable to those ofthe B. cereus donor strain. The hemolysin produced in B. subtilis seemed to be indistinguishable from cereolysin in its sensitivity to cholesterol, activation by dithiothreitol, and inactivation by antibodies raised against cereolysin. When the recombinant DNA carrying the cereolysin gene was used as a probe in hybridization experiments with chromosomal DNA from a streptolysin 0-producing strain of Streptococcus pyogenes or from üsteriolysin-producing strains of Usteria monoeytogenes, no positive hybridization signals were obtained. These data soggest that the genes for these three SH-activated cytolysins do not have extended sequence homology.
KW  - Biologie
Y1  - 1983
U6  - http://nbn-resolving.de/urn/resolver.pl?urn:nbn:de:bvb:20-opus-60596
ER  - 
TY  - JOUR
A1  - Härtlein, Michael
A1  - Schiessl, Sigrid
A1  - Wagner, Wilma
A1  - Rdest, Ursula
A1  - Kreft, Jürgen
A1  - Goebel, Werner
T1  - Transport of hemolysin by Escherichia coli
N2  - No abstract available
KW  - Biologie
KW  - Hemolysin
KW  - Escberichia coli
KW  - Gene cloning
KW  - Expression
KW  - Transport
Y1  - 1983
U6  - http://nbn-resolving.de/urn/resolver.pl?urn:nbn:de:bvb:20-opus-60619
ER  - 
TY  - JOUR
A1  - Scheer, Ulrich
A1  - Lanfranchi, Gerolamo
A1  - Rose, Kathleen M.
A1  - Franke, Werner W.
A1  - Ringertz, Nils R.
T1  - Migration of rat RNA polymerase I into chick erythrocyte nuclei undergoing reactivation in chick-rat heterokaryons
N2  - Transcriptionally inactive chick erythrocyte nudei were reactivated by Sendai virusinduced fusion of erythrocytes with rat L6j1 myoblasts. We used antibodies to trace the appearance of a specific protein engaged in transcription of a defined dass of genes, those coding for rRNA, during reactivation. Using immunofluorescence microscopy, we found increasing amounts of rat RNA polymerase I to appear, during a certain period of time after fusion, in the reforming nudeoli of the chick nudei. Amounts of rat RNA polymerase I sufficient to be detected by immunofluorescence microscopy had accumulated in the newly developed chick nudeoli 72- 190 h after fusion was initiated. This time interval coincides with the time when chick rRNA synthesis can first be detected. The results raise the possibility that during these stages of the reactivation process chick rRNA genes are transcribed by heterologous RNA polymerase I moleeules of rat origin.
Y1  - 1983
U6  - http://nbn-resolving.de/urn/resolver.pl?urn:nbn:de:bvb:20-opus-33232
ER  - 
TY  - JOUR
A1  - Kleinschmidt, Jürgen A.
A1  - Scheer, Ulrich
A1  - Dabauvalle, Marie-Christine
A1  - Bustin, Michael
A1  - Franke, Werner W.
T1  - High mobility group proteins of amphibian oocytes: a large storage pool of a soluble high mobility group-1-like protein and involvement in transcriptional events
N2  - No abstract available
Y1  - 1983
U6  - http://nbn-resolving.de/urn/resolver.pl?urn:nbn:de:bvb:20-opus-33250
ER  - 
TY  - JOUR
A1  - Viebrock, A
A1  - Perz, A
A1  - Sebald, Walter
T1  - Molecular cloning of middle-abundant mRNAs from Neurospora crassa
N2  - no abstract available
KW  - Neurospora crassa
Y1  - 1983
U6  - http://nbn-resolving.de/urn/resolver.pl?urn:nbn:de:bvb:20-opus-82033
ER  - 
TY  - JOUR
A1  - Gessler, Manfred
A1  - Barnekow, Angelika
T1  - Differential expression of the cellular oncogenes c-src and c-yes in embryonal and adult chicken tissues
N2  - The cellular onc-genes c-src and c-yes are expressed very differently during chicken embryonic development. The c-src mRNA and its translational product are detectable at high levels in brain extracts of chicken embryos and adult chickens, whereas muscle extracts show an age-dependent decrease in the amounts of c-src-specific mRNA and pp60<sup>c-src</sup> kinase activity. In contrast, the Ievels of c-yes mRNA in brain, heart, and muscle are relatively low in early embryonic stages and increase later on to values comparable to those found for liver, while in adult animals the pattern of c-yes expression is similar to that of the c-src gene. From the close correlation between the Ievels of pp60<sup>c-src</sup>, its enzymatic activity, and its corresponding mRNA at a given stage of development and in given tissues, it appears that the expression of pp60<sup>c-src</sup> is primarily controlled at the level of transcription. It is suggested that because of the different patterns of expression, the two cellular oncogenes, c-src and c-yes, play different roles in cell proliferation during early embryonic stages as weil as in ensuing differentiation processes.
KW  - Biochemie
Y1  - 1984
U6  - http://nbn-resolving.de/urn/resolver.pl?urn:nbn:de:bvb:20-opus-59289
ER  - 
TY  - JOUR
A1  - Arends, H.
A1  - Sebald, Walter
T1  - Nucleotide sequence of the cloned mRNA and gene of the ADP/ATP carrier from Neurospora crassa
N2  - A cDNA complementary to the mRNA of the ADPIATP carrier from Neurospora crassa was identified among ordered cDNA clones by hybridizing total polyadenylated RNA to pools of 96 cDNA recombinant plasmids and subsequent cellfree translation of hybridization-selected mRNA. Further carrier cDNAs were found by colony fdter hybridization at a frequency of 0.2-0.3%. The gene of the carrier was cloned and isolated on a 4.6-kbp EcoRl fragment of total Neurospora DNA, and the start of the mRNA was determined by Sl nuclease mapping. From the nucleotide sequence of the cDNA and the genomic DNA, the primary structure of the gene, of the mRNA and of the ADP I ATP carrier protein could be deduced. The gene occurs in a single copy in the genome and related genes are absent. It contains two short introns, and a pyrimidine-rieb promoter region. The mRNA has a 46-bp 5 1 end and a 219-bp 3 1 end. There is an open reading frame coding for the 313 amino acid residues of the Neurospora carrier protein. The amino acid sequence is homologous in 148 positions with the established primary structure of the beef heart carrier.
KW  - Biochemie
KW  - mitochondrial ADP
KW  - ATP carrier
KW  - Neurospora crassa
KW  - mRNA and gene
KW  - nucleotide sequence
KW  - hybrid-selected translation
Y1  - 1984
U6  - http://nbn-resolving.de/urn/resolver.pl?urn:nbn:de:bvb:20-opus-62684
ER  -