Abstract
I have analysed the duplex-to-hairpin transition of large inverted duplications with a short asymmetric center which are found in the amplified DNA of two mammalian cell lines resistant to cytotoxic drugs. Psoralen crosslinking experiments establish that this transition does not occur in vivo, but takes place in a significant portion of the palindromes during genomic DNA purification, at the phenol-chloroform extraction step. The introduction of single strand nicks in the DNA by gamma irradiation prior to its purification does not prevent hairpin formation but instead facilitates it. These results show that the rate-limiting step of the duplex-to-hairpin transition does not require negative supercoiling, and that transient melting of large segments of cellular DNA occurs during phenol-chloroform extraction. I also show, and discuss the fact, that only cellular DNA, and not cloned palindromic DNA, is able to undergo hairpin formation by this mechanism. These results bear practical implications for the study of inverted repeated DNA sequences in eukaryotic cells.
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.
- Cole R. S. Inactivation of Escherichia coli, F' episomes at transfer, and bacteriophage lambda by psoralen plus 360-nm light: significance of deoxyribonucleic acid cross-links. J Bacteriol. 1971 Sep;107(3):846–852. doi: 10.1128/jb.107.3.846-852.1971. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Cole R. S. Light-induced cross-linking of DNA in the presence of a furocoumarin (psoralen). Studies with phage lambda, Escherichia coli, and mouse leukemia cells. Biochim Biophys Acta. 1970 Sep 17;217(1):30–39. doi: 10.1016/0005-2787(70)90119-x. [DOI] [PubMed] [Google Scholar]
- Courey A. J., Wang J. C. Cruciform formation in a negatively supercoiled DNA may be kinetically forbidden under physiological conditions. Cell. 1983 Jul;33(3):817–829. doi: 10.1016/0092-8674(83)90024-7. [DOI] [PubMed] [Google Scholar]
- Ford M., Davies B., Griffiths M., Wilson J., Fried M. Isolation of a gene enhancer within an amplified inverted duplication after "expression selection". Proc Natl Acad Sci U S A. 1985 May;82(10):3370–3374. doi: 10.1073/pnas.82.10.3370. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Ford M., Fried M. Large inverted duplications are associated with gene amplification. Cell. 1986 May 9;45(3):425–430. doi: 10.1016/0092-8674(86)90328-4. [DOI] [PubMed] [Google Scholar]
- Gellert M., Mizuuchi K., O'Dea M. H., Ohmori H., Tomizawa J. DNA gyrase and DNA supercoiling. Cold Spring Harb Symp Quant Biol. 1979;43(Pt 1):35–40. doi: 10.1101/sqb.1979.043.01.007. [DOI] [PubMed] [Google Scholar]
- Gough G. W., Sullivan K. M., Lilley D. M. The structure of cruciforms in supercoiled DNA: probing the single-stranded character of nucleotide bases with bisulphite. EMBO J. 1986 Jan;5(1):191–196. doi: 10.1002/j.1460-2075.1986.tb04195.x. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Guéron M., Kochoyan M., Leroy J. L. A single mode of DNA base-pair opening drives imino proton exchange. Nature. 1987 Jul 2;328(6125):89–92. doi: 10.1038/328089a0. [DOI] [PubMed] [Google Scholar]
- Heartlein M. W., Latt S. A. Amplified inverted duplications within and adjacent to heterologous selectable DNA. Nucleic Acids Res. 1989 Feb 25;17(4):1697–1716. doi: 10.1093/nar/17.4.1697. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Herrmann B. G., Barlow D. P., Lehrach H. A large inverted duplication allows homologous recombination between chromosomes heterozygous for the proximal t complex inversion. Cell. 1987 Mar 13;48(5):813–825. doi: 10.1016/0092-8674(87)90078-x. [DOI] [PubMed] [Google Scholar]
- Hilbers C. W., Haasnoot C. A., de Bruin S. H., Joordens J. J., van der Marel G. A., van Boom J. H. Hairpin formation in synthetic oligonucleotides. Biochimie. 1985 Jul-Aug;67(7-8):685–695. doi: 10.1016/s0300-9084(85)80156-5. [DOI] [PubMed] [Google Scholar]
- Hyrien O., Debatisse M., Buttin G., de Saint Vincent B. R. A hotspot for novel amplification joints in a mosaic of Alu-like repeats and palindromic A + T-rich DNA. EMBO J. 1987 Aug;6(8):2401–2408. doi: 10.1002/j.1460-2075.1987.tb02518.x. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Hyrien O., Debatisse M., Buttin G., de Saint Vincent B. R. The multicopy appearance of a large inverted duplication and the sequence at the inversion joint suggest a new model for gene amplification. EMBO J. 1988 Feb;7(2):407–417. doi: 10.1002/j.1460-2075.1988.tb02828.x. [DOI] [PMC free article] [PubMed] [Google Scholar]
- LEVINE L., GORDON J. A., JENCKS W. P. The relationship of structure to the effectiveness of denaturing agents for deoxyribonucleic acid. Biochemistry. 1963 Jan-Feb;2:168–175. doi: 10.1021/bi00901a030. [DOI] [PubMed] [Google Scholar]
- Legouy E., Fossar N., Lhomond G., Brison O. Structure of four amplified DNA novel joints. Somat Cell Mol Genet. 1989 Jul;15(4):309–320. doi: 10.1007/BF01534970. [DOI] [PubMed] [Google Scholar]
- Lilley D. M. DNA opens up--supercoiling and heavy breathing. Trends Genet. 1988 Apr;4(4):111–114. doi: 10.1016/0168-9525(88)90099-6. [DOI] [PubMed] [Google Scholar]
- Lilley D. M. The inverted repeat as a recognizable structural feature in supercoiled DNA molecules. Proc Natl Acad Sci U S A. 1980 Nov;77(11):6468–6472. doi: 10.1073/pnas.77.11.6468. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Looney J. E., Hamlin J. L. Isolation of the amplified dihydrofolate reductase domain from methotrexate-resistant Chinese hamster ovary cells. Mol Cell Biol. 1987 Feb;7(2):569–577. doi: 10.1128/mcb.7.2.569. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Nalbantoglu J., Meuth M. DNA amplification--deletion in a spontaneous mutation of the hamster aprt locus: structure and sequence of the novel joint. Nucleic Acids Res. 1986 Nov 11;14(21):8361–8371. doi: 10.1093/nar/14.21.8361. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Panayotatos N., Fontaine A. A native cruciform DNA structure probed in bacteria by recombinant T7 endonuclease. J Biol Chem. 1987 Aug 15;262(23):11364–11368. [PubMed] [Google Scholar]
- Panayotatos N., Wells R. D. Cruciform structures in supercoiled DNA. Nature. 1981 Feb 5;289(5797):466–470. doi: 10.1038/289466a0. [DOI] [PubMed] [Google Scholar]
- Passananti C., Davies B., Ford M., Fried M. Structure of an inverted duplication formed as a first step in a gene amplification event: implications for a model of gene amplification. EMBO J. 1987 Jun;6(6):1697–1703. doi: 10.1002/j.1460-2075.1987.tb02420.x. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Ruiz J. C., Wahl G. M. Formation of an inverted duplication can be an initial step in gene amplification. Mol Cell Biol. 1988 Oct;8(10):4302–4313. doi: 10.1128/mcb.8.10.4302. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Russev G., Vassilev L. Isolation of a DNA fraction from Ehrlich ascites tumour cells containing the putative origin of replication. J Mol Biol. 1982 Oct 15;161(1):77–87. doi: 10.1016/0022-2836(82)90279-0. [DOI] [PubMed] [Google Scholar]
- Saito I., Stark G. R. Charomids: cosmid vectors for efficient cloning and mapping of large or small restriction fragments. Proc Natl Acad Sci U S A. 1986 Nov;83(22):8664–8668. doi: 10.1073/pnas.83.22.8664. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Shurvinton C. E., Stahl M. M., Stahl F. W. Large palindromes in the lambda phage genome are preserved in a rec+ host by inhibiting lambda DNA replication. Proc Natl Acad Sci U S A. 1987 Mar;84(6):1624–1628. doi: 10.1073/pnas.84.6.1624. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Sinden R. R., Broyles S. S., Pettijohn D. E. Perfect palindromic lac operator DNA sequence exists as a stable cruciform structure in supercoiled DNA in vitro but not in vivo. Proc Natl Acad Sci U S A. 1983 Apr;80(7):1797–1801. doi: 10.1073/pnas.80.7.1797. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Sinden R. R., Carlson J. O., Pettijohn D. E. Torsional tension in the DNA double helix measured with trimethylpsoralen in living E. coli cells: analogous measurements in insect and human cells. Cell. 1980 Oct;21(3):773–783. doi: 10.1016/0092-8674(80)90440-7. [DOI] [PubMed] [Google Scholar]
- Sullivan K. M., Lilley D. M. A dominant influence of flanking sequences on a local structural transition in DNA. Cell. 1986 Dec 5;47(5):817–827. doi: 10.1016/0092-8674(86)90524-6. [DOI] [PubMed] [Google Scholar]
- Sullivan K. M., Lilley D. M. Helix stability and the mechanism of cruciform extrusion in supercoiled DNA molecules. Nucleic Acids Res. 1988 Feb 11;16(3):1079–1093. doi: 10.1093/nar/16.3.1079. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Wells R. D. Unusual DNA structures. J Biol Chem. 1988 Jan 25;263(3):1095–1098. [PubMed] [Google Scholar]
- Zannis-Hadjopoulos M., Frappier L., Khoury M., Price G. B. Effect of anti-cruciform DNA monoclonal antibodies on DNA replication. EMBO J. 1988 Jun;7(6):1837–1844. doi: 10.1002/j.1460-2075.1988.tb03016.x. [DOI] [PMC free article] [PubMed] [Google Scholar]