An anti-Z-antibody-binding region between PM2-DNA map units 0.05 and 0.18, containing approx. 25% of the bound PM2 antibody molecules (1,2) has been sequenced. Analysis of this PM2 DNA sequence from map units 0.00 to 0.175 demonstrates that alternating purine/pyrimidine tracts capable of adopting the left-handed conformation are present within this antibody-binding region. Longer (GC)n-rich tracts are clustered together and comprise seven alternating purine/pyrimidine-rich areas (48%–84%) ranging from 19 to 142 nucleotides in length. The DNA located between these alternating purine/pyrimidine-rich areas exhibit a low level (0%–19%) of this sequence arrangement. There is a very strong correlation between the alternating purine/pyrimidine-rich areas and the anti-Z-DNA-IgG-binding sites. Nucleotides 1461–1583 of the PM2-DNA genome encode the bacteriophage capsid protein IV. One of the PM2 left-handed sites is located within this protein-coding sequence; a B-to-Z transition within this site may be involved in protein-IV gene regulation in vivo.
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Research Article|
October 01 1984
Sequence analysis of a PM2-DNA anti-Z-IgG-binding region
F. D. Miller;
F. D. Miller
1Department of Medical Biochemistry, The University of Calgary, Calgary, Alberta, Canada T2N 4N1
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R. J. Winkfein;
R. J. Winkfein
1Department of Medical Biochemistry, The University of Calgary, Calgary, Alberta, Canada T2N 4N1
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J. B. Rattner;
J. B. Rattner
2Department of Anatomy, The University of Calgary, Calgary, Alberta, Canada T2N 4N1
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J. H. Van de Sande
J. H. Van de Sande
1Department of Medical Biochemistry, The University of Calgary, Calgary, Alberta, Canada T2N 4N1
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Publisher: Portland Press Ltd
Received:
August 21 1984
Online ISSN: 1573-4935
Print ISSN: 0144-8463
© 1984 The Biochemical Society
1984
Biosci Rep (1984) 4 (10): 885–895.
Article history
Received:
August 21 1984
Citation
F. D. Miller, R. J. Winkfein, J. B. Rattner, J. H. Van de Sande; Sequence analysis of a PM2-DNA anti-Z-IgG-binding region. Biosci Rep 1 October 1984; 4 (10): 885–895. doi: https://doi.org/10.1007/BF01138171
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