Abstract
Duplex DNA containing oligo(dG.dC)-rich clusters can be isolated by specific binding to poly(rC)-Sephadex. This binding, probably mediated by the formation of an oligo(dG.dC)rC+ triple helix, is optimal at pH 5 in 50% formamide, 2 M LiCl; the bound DNA is recovered by elution at pH 7.5. Using this method we find that the viral DNAs PM2, lambda and SV40 contain at least 1, 1 and 2 sites for binding to poly(rC)-Sephadex, respectively. These binding sites have been mapped in the case of SV40; the binding sites can in turn be used for physical mapping studies of DNAs containing (dG.dC) clusters. Inspection of the sequence of the bound fragments of SV40 DNA shows that a (dG.dC)6-7 tract is required for the binding of duplex DNA to poly(rC)-Sephadex. Although about 60% of rabbit DNA cleaved with restriction endonuclease KpnI binds to poly(rC)-Sephadex, no binding is observed for the 5.1 kb DNA fragment generated by KpnI digestion, which contains the rabbit beta-globin gene. This indicates that oligo(dG.dC) clusters are not found close to the rabbit beta-globin gene.
Full text
PDF












Images in this article
Selected References
These references are in PubMed. This may not be the complete list of references from this article.
- Brahms J., Maurizot J. C., Michelson A. M. Conformation and thermodynamic properties of oligocytidylic acids. J Mol Biol. 1967 May 14;25(3):465–480. doi: 10.1016/0022-2836(67)90199-4. [DOI] [PubMed] [Google Scholar]
- Flavell R. A., Van Den Berg F. M. The isolation of duplex DNA containing (dA-dT) clusters by affinity chromatography on poly (U) sephadex. FEBS Lett. 1975 Oct 15;58(1):90–93. doi: 10.1016/0014-5793(75)80232-8. [DOI] [PubMed] [Google Scholar]
- Flavell R. A., Van den Berg F. M., Grosveld G. C. Isolation and characterization of the oligo(dA-dT) clusters and their flanking DNA segments in the rabbit genome. J Mol Biol. 1977 Oct 5;115(4):715–735. doi: 10.1016/0022-2836(77)90111-5. [DOI] [PubMed] [Google Scholar]
- Jeffreys A. J., Flavell R. A. A physical map of the DNA regions flanking the rabbit beta-globin gene. Cell. 1977 Oct;12(2):429–439. doi: 10.1016/0092-8674(77)90119-2. [DOI] [PubMed] [Google Scholar]
- Jeffreys A. J., Flavell R. A. The rabbit beta-globin gene contains a large large insert in the coding sequence. Cell. 1977 Dec;12(4):1097–1108. doi: 10.1016/0092-8674(77)90172-6. [DOI] [PubMed] [Google Scholar]
- Maniatis T., Kee S. G., Efstratiadis A., Kafatos F. C. Amplification and characterization of a beta-globin gene synthesized in vitro. Cell. 1976 Jun;8(2):163–182. doi: 10.1016/0092-8674(76)90001-5. [DOI] [PubMed] [Google Scholar]
- Sanger F., Air G. M., Barrell B. G., Brown N. L., Coulson A. R., Fiddes C. A., Hutchison C. A., Slocombe P. M., Smith M. Nucleotide sequence of bacteriophage phi X174 DNA. Nature. 1977 Feb 24;265(5596):687–695. doi: 10.1038/265687a0. [DOI] [PubMed] [Google Scholar]
- Shenkin A., Burdon R. H. Deoxyadenylate-rich and deoxyguanylate-rich regions in mammalian DNA. J Mol Biol. 1974 May 5;85(1):19–39. doi: 10.1016/0022-2836(74)90126-0. [DOI] [PubMed] [Google Scholar]
- Southern E. M. Detection of specific sequences among DNA fragments separated by gel electrophoresis. J Mol Biol. 1975 Nov 5;98(3):503–517. doi: 10.1016/s0022-2836(75)80083-0. [DOI] [PubMed] [Google Scholar]
- Thiele D., Guschlbauer W. Protonated polynucleotide structures. IX. Disproportionation of poly (G)-poly (C) in acid medium. Biopolymers. 1971;10(1):143–157. doi: 10.1002/bip.360100111. [DOI] [PubMed] [Google Scholar]
- Wu R., Padmanabhan R., Bambara R. Nucleotide sequence analysis of bacteriophage DNA. Methods Enzymol. 1974;29:231–253. doi: 10.1016/0076-6879(74)29025-6. [DOI] [PubMed] [Google Scholar]


