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. 1998 Aug 15;26(16):3837–3844. doi: 10.1093/nar/26.16.3837

2-Aminopurine fluorescence studies of base stacking interactions at abasic sites in DNA: metal-ion and base sequence effects.

J T Stivers 1
PMCID: PMC147768  PMID: 9685503

Abstract

Metal-ion and sequence dependent changes in the stacking interactions of bases surrounding abasic (AB) sites in 10 different DNA duplexes were examined by incorporating the fluorescent nucleotide probe 2-aminopurine (2-AP), opposite to the site (AB-APopp) or adjacent to the site (AB-APadj) on either strand. A detailed study of the fluorescence emission and excitation spectra of these AB duplexes and their corresponding parent duplexes indicates that AB-APoppis significantly less stacked than 2-AP in the corresponding normal duplex. In general, AB-APadjon the AB strand is stacked, but AB-APadjon the opposite strand shows destabilized stacking interactions. The results also indicate that divalent cation binding to the AB duplexes contributes to destabilizaton of the base stacking interactions of AB-APopp, but has little or no effect on the stacking interactions of AB-APadj. Consistent with these results, the fluorescence of AB-APoppis 18-30-fold more sensitive to an externally added quenching agent than the parent normal duplex. When uracil DNA glycosylase binds to AB-APoppin the presence of 2.5 mM MgCl2, a 3-fold decrease in fluorescence is observed ( K d = 400 +/- 90 nM) indicating that the unstacked 2-APoppbecomes more stacked upon binding. On the basis of these fluorescence studies a model for the local base stacking interactions at these AB sites is proposed.

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Selected References

These references are in PubMed. This may not be the complete list of references from this article.

  1. Allan B. W., Reich N. O. Targeted base stacking disruption by the EcoRI DNA methyltransferase. Biochemistry. 1996 Nov 26;35(47):14757–14762. doi: 10.1021/bi9615708. [DOI] [PubMed] [Google Scholar]
  2. Bailly V., Verly W. G. AP endonucleases and AP lyases. Nucleic Acids Res. 1989 May 11;17(9):3617–3618. doi: 10.1093/nar/17.9.3617. [DOI] [PMC free article] [PubMed] [Google Scholar]
  3. Bloom L. B., Otto M. R., Eritja R., Reha-Krantz L. J., Goodman M. F., Beechem J. M. Pre-steady-state kinetic analysis of sequence-dependent nucleotide excision by the 3'-exonuclease activity of bacteriophage T4 DNA polymerase. Biochemistry. 1994 Jun 21;33(24):7576–7586. doi: 10.1021/bi00190a010. [DOI] [PubMed] [Google Scholar]
  4. Coppel Y., Berthet N., Coulombeau C., Coulombeau C., Garcia J., Lhomme J. Solution conformation of an abasic DNA undecamer duplex d(CGCACXCACGC) x d(GCGTGTGTGCG): the unpaired thymine stacks inside the helix. Biochemistry. 1997 Apr 22;36(16):4817–4830. doi: 10.1021/bi962677y. [DOI] [PubMed] [Google Scholar]
  5. Cuniasse P., Fazakerley G. V., Guschlbauer W., Kaplan B. E., Sowers L. C. The abasic site as a challenge to DNA polymerase. A nuclear magnetic resonance study of G, C and T opposite a model abasic site. J Mol Biol. 1990 May 20;213(2):303–314. doi: 10.1016/S0022-2836(05)80192-5. [DOI] [PubMed] [Google Scholar]
  6. Cuniasse P., Sowers L. C., Eritja R., Kaplan B., Goodman M. F., Cognet J. A., LeBret M., Guschlbauer W., Fazakerley G. V. An abasic site in DNA. Solution conformation determined by proton NMR and molecular mechanics calculations. Nucleic Acids Res. 1987 Oct 12;15(19):8003–8022. doi: 10.1093/nar/15.19.8003. [DOI] [PMC free article] [PubMed] [Google Scholar]
  7. Demple B., Harrison L. Repair of oxidative damage to DNA: enzymology and biology. Annu Rev Biochem. 1994;63:915–948. doi: 10.1146/annurev.bi.63.070194.004411. [DOI] [PubMed] [Google Scholar]
  8. Fagan P. A., Fàbrega C., Eritja R., Goodman M. F., Wemmer D. E. NMR study of the conformation of the 2-aminopurine:cytosine mismatch in DNA. Biochemistry. 1996 Apr 2;35(13):4026–4033. doi: 10.1021/bi952657g. [DOI] [PubMed] [Google Scholar]
  9. Fazakerley G. V., Sowers L. C., Eritja R., Kaplan B. E., Goodman M. F. NMR studies on an oligodeoxynucleotide containing 2-aminopurine opposite adenine. Biochemistry. 1987 Sep 8;26(18):5641–5646. doi: 10.1021/bi00392a009. [DOI] [PubMed] [Google Scholar]
  10. Goljer I., Kumar S., Bolton P. H. Refined solution structure of a DNA heteroduplex containing an aldehydic abasic site. J Biol Chem. 1995 Sep 29;270(39):22980–22987. doi: 10.1074/jbc.270.39.22980. [DOI] [PubMed] [Google Scholar]
  11. Guest C. R., Hochstrasser R. A., Sowers L. C., Millar D. P. Dynamics of mismatched base pairs in DNA. Biochemistry. 1991 Apr 2;30(13):3271–3279. doi: 10.1021/bi00227a015. [DOI] [PubMed] [Google Scholar]
  12. Kalnik M. W., Chang C. N., Grollman A. P., Patel D. J. NMR studies of abasic sites in DNA duplexes: deoxyadenosine stacks into the helix opposite the cyclic analogue of 2-deoxyribose. Biochemistry. 1988 Feb 9;27(3):924–931. doi: 10.1021/bi00403a013. [DOI] [PubMed] [Google Scholar]
  13. Kalnik M. W., Chang C. N., Johnson F., Grollman A. P., Patel D. J. NMR studies of abasic sites in DNA duplexes: deoxyadenosine stacks into the helix opposite acyclic lesions. Biochemistry. 1989 Apr 18;28(8):3373–3383. doi: 10.1021/bi00434a037. [DOI] [PubMed] [Google Scholar]
  14. Kalnik M. W., Norman D. G., Li B. F., Swann P. F., Patel D. J. Conformational transitions in thymidine bulge-containing deoxytridecanucleotide duplexes. Role of flanking sequence and temperature in modulating the equilibrium between looped out and stacked thymidine bulge states. J Biol Chem. 1990 Jan 15;265(2):636–647. [PubMed] [Google Scholar]
  15. Kalnik M. W., Norman D. G., Zagorski M. G., Swann P. F., Patel D. J. Conformational transitions in cytidine bulge-containing deoxytridecanucleotide duplexes: extra cytidine equilibrates between looped out (low temperature) and stacked (elevated temperature) conformations in solution. Biochemistry. 1989 Jan 10;28(1):294–303. doi: 10.1021/bi00427a040. [DOI] [PubMed] [Google Scholar]
  16. Kollman P. A., Weiner P. K., Dearing A. Studies of nucleotide conformations and interactions. The relative stabilities of double-helical B-DNA sequence isomers. Biopolymers. 1981 Dec;20(12):2583–2621. doi: 10.1002/bip.1981.360201208. [DOI] [PubMed] [Google Scholar]
  17. Law S. M., Eritja R., Goodman M. F., Breslauer K. J. Spectroscopic and calorimetric characterizations of DNA duplexes containing 2-aminopurine. Biochemistry. 1996 Sep 24;35(38):12329–12337. doi: 10.1021/bi9614545. [DOI] [PubMed] [Google Scholar]
  18. Lindahl T., Ljungquist S., Siegert W., Nyberg B., Sperens B. DNA N-glycosidases: properties of uracil-DNA glycosidase from Escherichia coli. J Biol Chem. 1977 May 25;252(10):3286–3294. [PubMed] [Google Scholar]
  19. Lindahl T., Nyberg B. Rate of depurination of native deoxyribonucleic acid. Biochemistry. 1972 Sep 12;11(19):3610–3618. doi: 10.1021/bi00769a018. [DOI] [PubMed] [Google Scholar]
  20. Mazumder A., Gerlt J. A., Absalon M. J., Stubbe J., Cunningham R. P., Withka J., Bolton P. H. Stereochemical studies of the beta-elimination reactions at aldehydic abasic sites in DNA: endonuclease III from Escherichia coli, sodium hydroxide, and Lys-Trp-Lys. Biochemistry. 1991 Jan 29;30(4):1119–1126. doi: 10.1021/bi00218a033. [DOI] [PubMed] [Google Scholar]
  21. McCullough A. K., Dodson M. L., Schärer O. D., Lloyd R. S. The role of base flipping in damage recognition and catalysis by T4 endonuclease V. J Biol Chem. 1997 Oct 24;272(43):27210–27217. doi: 10.1074/jbc.272.43.27210. [DOI] [PubMed] [Google Scholar]
  22. Menger M., Tuschl T., Eckstein F., Porschke D. Mg(2+)-dependent conformational changes in the hammerhead ribozyme. Biochemistry. 1996 Nov 26;35(47):14710–14716. doi: 10.1021/bi960440w. [DOI] [PubMed] [Google Scholar]
  23. Millican T. A., Mock G. A., Chauncey M. A., Patel T. P., Eaton M. A., Gunning J., Cutbush S. D., Neidle S., Mann J. Synthesis and biophysical studies of short oligodeoxynucleotides with novel modifications: a possible approach to the problem of mixed base oligodeoxynucleotide synthesis. Nucleic Acids Res. 1984 Oct 11;12(19):7435–7453. doi: 10.1093/nar/12.19.7435. [DOI] [PMC free article] [PubMed] [Google Scholar]
  24. Moe J. G., Russu I. M. Kinetics and energetics of base-pair opening in 5'-d(CGCGAATTCGCG)-3' and a substituted dodecamer containing G.T mismatches. Biochemistry. 1992 Sep 15;31(36):8421–8428. doi: 10.1021/bi00151a005. [DOI] [PubMed] [Google Scholar]
  25. Nordlund T. M., Andersson S., Nilsson L., Rigler R., Gräslund A., McLaughlin L. W. Structure and dynamics of a fluorescent DNA oligomer containing the EcoRI recognition sequence: fluorescence, molecular dynamics, and NMR studies. Biochemistry. 1989 Nov 14;28(23):9095–9103. doi: 10.1021/bi00449a021. [DOI] [PubMed] [Google Scholar]
  26. Nordlund T. M., Xu D., Evans K. O. Excitation energy transfer in DNA: duplex melting and transfer from normal bases to 2-aminopurine. Biochemistry. 1993 Nov 16;32(45):12090–12095. doi: 10.1021/bi00096a020. [DOI] [PubMed] [Google Scholar]
  27. Record M. T., Jr, Anderson C. F., Lohman T. M. Thermodynamic analysis of ion effects on the binding and conformational equilibria of proteins and nucleic acids: the roles of ion association or release, screening, and ion effects on water activity. Q Rev Biophys. 1978 May;11(2):103–178. doi: 10.1017/s003358350000202x. [DOI] [PubMed] [Google Scholar]
  28. Singh M. P., Hill G. C., Péoc'h D., Rayner B., Imbach J. L., Lown J. W. High-field NMR and restrained molecular modeling studies on a DNA heteroduplex containing a modified apurinic abasic site in the form of covalently linked 9-aminoellipticine. Biochemistry. 1994 Aug 30;33(34):10271–10285. doi: 10.1021/bi00200a007. [DOI] [PubMed] [Google Scholar]
  29. Slupphaug G., Mol C. D., Kavli B., Arvai A. S., Krokan H. E., Tainer J. A. A nucleotide-flipping mechanism from the structure of human uracil-DNA glycosylase bound to DNA. Nature. 1996 Nov 7;384(6604):87–92. doi: 10.1038/384087a0. [DOI] [PubMed] [Google Scholar]
  30. Takeshita M., Chang C. N., Johnson F., Will S., Grollman A. P. Oligodeoxynucleotides containing synthetic abasic sites. Model substrates for DNA polymerases and apurinic/apyrimidinic endonucleases. J Biol Chem. 1987 Jul 25;262(21):10171–10179. [PubMed] [Google Scholar]
  31. Withka J. M., Wilde J. A., Bolton P. H., Mazumder A., Gerlt J. A. Characterization of conformational features of DNA heteroduplexes containing aldehydic abasic sites. Biochemistry. 1991 Oct 15;30(41):9931–9940. doi: 10.1021/bi00105a017. [DOI] [PubMed] [Google Scholar]
  32. Wu P. G., Nordlund T. M., Gildea B., McLaughlin L. W. Base stacking and unstacking as determined from a DNA decamer containing a fluorescent base. Biochemistry. 1990 Jul 10;29(27):6508–6514. doi: 10.1021/bi00479a024. [DOI] [PubMed] [Google Scholar]
  33. Xu D., Evans K. O., Nordlund T. M. Melting and premelting transitions of an oligomer measured by DNA base fluorescence and absorption. Biochemistry. 1994 Aug 16;33(32):9592–9599. doi: 10.1021/bi00198a027. [DOI] [PubMed] [Google Scholar]
  34. van den Hoogen Y. T., van Beuzekom A. A., van den Elst H., van der Marel G. A., van Boom J. H., Altona C. Extra thymidine stacks into the d(CTGGTGCGG).d(CCGCCCAG) duplex. An NMR and model-building study. Nucleic Acids Res. 1988 Apr 11;16(7):2971–2986. doi: 10.1093/nar/16.7.2971. [DOI] [PMC free article] [PubMed] [Google Scholar]

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