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  • 1
    Digitale Medien
    Digitale Medien
    Molecular evolution of the carbonic anhydrase genes: Calculation of divergence time for mouse carbonic anhydrase I and II (1986)
    Springer
    Journal of molecular evolution 23 (1986), S. 294-299 
    Details
    ISSN: 1432-1432
    Schlagwort(e): cDNA cloning ; Nucleotide sequence comparison
    Quelle: Springer Online Journal Archives 1860-2000
    Thema: Biologie
    Notizen: Summary A cDNA clone in pBR322 that cross-hybridizes with a mouse carbonic anhydrase form II (CAII) probe has been sequenced and identified as mouse carbonic anhydrase form I (CAI). The 1224-base-pair clone encodes the entire 260-amino-acid protein and appears to contain an Alu-like element in the 3′ untranslated region. The deduced amino acid sequence exhibits 77% homology to human CAI and contains 17 of the 20 residues that are considered unique to and invariant for all mammalian CAI isozymes. The results of a detailed comparison of the nucleic acid sequences spanning the coding regions of mouse CAI and rabbit CAI have been used to calibrate an evolutionary clock for the carbonic anhydrases (CAs). These data have been applied to a comparison of the mouse CAI and CAII nucleic acid sequences to calculate the divergence time between the two genes. The divergence-time calculation provides the first estimation of the evolutionary relationship between CAs based entirely on nucleotide sequence comparison.
    Materialart: Digitale Medien
    URL: http://dx.doi.org/10.1007/BF02100637
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  • 2
    Digitale Medien
    Digitale Medien
    Structure of the glycoprotein gene in rabies virus (1981)
    [s.l.] : Nature Publishing Group
    Nature 294 (1981), S. 275-278 
    Details
    ISSN: 1476-4687
    Quelle: Nature Archives 1869 - 2009
    Thema: Biologie , Chemie und Pharmazie , Medizin , Allgemeine Naturwissenschaft , Physik
    Notizen: [Auszug] The five rabies virus-specific mRNAs for L, G, N, MI and M2 proteins have been characterized by sucrose gradient3 and gel analysis2: L mRNA sediments at 〉28S, glycoprotein (G) mRNA at 18S, nucleocapsid (N) mRNA at 16S and matrix (Mt and M2) mRNAs at 12S. For the cloning of the G mRNA, RNA ...
    Materialart: Digitale Medien
    URL: http://dx.doi.org/10.1038/294275a0
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  • 3
    Digitale Medien
    Digitale Medien
    Evaluation of Foreign Gene Codon Optimization in Yeast: Expression of a Mouse IG Kappa Chain (1991)
    [s.l.] : Nature Publishing Company
    Nature biotechnology 9 (1991), S. 1386-1389 
    Details
    ISSN: 1546-1696
    Quelle: Nature Archives 1869 - 2009
    Thema: Biologie , Werkstoffwissenschaften, Fertigungsverfahren, Fertigung
    Notizen: [Auszug] We have optimized the codons in an immunoglobulin kappa chain gene to those preferred in the yeast Saccharomyces cerevisiae. The mutant and wild type kappa chain genes were each fused with a synthetic invertase signal peptide that also contained only yeast–preferred codons, and expressed in ...
    Materialart: Digitale Medien
    URL: http://dx.doi.org/10.1038/nbt1291-1386
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  • 4
    Digitale Medien
    Digitale Medien
    Assignment of mouse beta-spectrin gene to chromosome 12 (1987)
    Springer
    Somatic cell and molecular genetics 13 (1987), S. 93-97 
    Details
    ISSN: 1572-9931
    Quelle: Springer Online Journal Archives 1860-2000
    Thema: Biologie , Medizin
    Notizen: Abstract The structural gene for the Β-subunit of the mouse erythrocyte spectrin, hereinafter designated as Sp-b, was assigned to the mouse chromosome 12. This assignment was made by Southern analysis of genomic DNA from mouse X Chinese hamster hybrid cells using cloned mouse erythrocyte Β-spectrin cDNA as a probe. In the PstI-digested genomic hamster cell DNA a single band of 2.0 kb was detected, whereas PstI-digested mouse DNA gave a band of 4.2 kb, when probed with the mouse erythroid Β-spectrin cDNA clone. This allowed us to analyze a panel of mouse X Chinese hamster somatic cell hybrids to map this gene to chromosome 12. Interestingly, this assignment is different from that observed for the α-subunit of spectrin, which has been mapped to chromosome 1 in mouse. These results serve as a basis for further genetic characterization of the mouse hemolytic anemias.
    Materialart: Digitale Medien
    URL: http://dx.doi.org/10.1007/BF02422304
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