Literature DB >> 8443159

Specific recognition of CG base pairs by 2-deoxynebularine within the purine.purine.pyrimidine triple-helix motif.

H U Stilz1, P B Dervan.   

Abstract

The sequence-specific recognition of double-helical DNA by oligodeoxyribonucleotide-directed triple-helix formation is limited mostly to purine tracts. Within the geometric constraints of the phosphate-deoxyribose position of a purine-purine-pyrimidine triple-helical structure, model building studies suggested that the deoxyribonucleoside 2'-deoxynebularine (dN) might form one specific hydrogen bond with cytosine (C) or adenine (A) of Watson-Crick cytosine-guanine (CG) or adenine-thymine (AT) base pairs. 2-Deoxynebularine (dN) was incorporated by automated methods into purine-rich oligodeoxyribonucleotides. From affinity cleavage analysis, the stabilities of base triplets within a purine.purine.pyrimidine (Pu.Pu.Py) triple helix were found to decrease in the order N.CG approximately N.AT >> N.GC approximately N.TA (pH 7.4, 37 degrees C). Oligodeoxyribonucleotides containing two N residues were shown to bind specifically within plasmid DNA a single 15 base pair site of the human immunodeficiency virus genome containing two CG base pairs within a purine tract. This binding event occurs under physiologically relevant pH and temperature (pH 7.4, 37 degrees C) and demonstrates the utility of the new base. Quantitative affinity cleavage titration reveals that, in the particular sequence studied, an N.CG base triplet interaction results in a stabilization of the local triple-helical structure by 1 kcal.mol-1 (10 mM NaCl, 1 mM spermine tetrahydrochloride, 50 mM Tris-acetate, pH 7.4, 4 degrees C) compared to an A.CG base triplet mismatch.

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Year:  1993        PMID: 8443159     DOI: 10.1021/bi00060a008

Source DB:  PubMed          Journal:  Biochemistry        ISSN: 0006-2960            Impact factor:   3.162


  16 in total

Review 1.  Therapeutic modulation of endogenous gene function by agents with designed DNA-sequence specificities.

Authors:  Taco G Uil; Hidde J Haisma; Marianne G Rots
Journal:  Nucleic Acids Res       Date:  2003-11-01       Impact factor: 16.971

2.  Triplex formation by oligonucleotides containing novel deoxycytidine derivatives.

Authors:  C Y Huang; G Bi; P S Miller
Journal:  Nucleic Acids Res       Date:  1996-07-01       Impact factor: 16.971

3.  A computational study of expanded heterocyclic nucleosides in DNA.

Authors:  Peter I O'Daniel; Malcolm Jefferson; Olaf Wiest; Katherine L Seley-Radtke
Journal:  J Biomol Struct Dyn       Date:  2008-12

4.  Triple-helix formation in the antiparallel binding motif of oligodeoxynucleotides containing N(9)- and N(7)-2-aminopurine deoxynucleosides.

Authors:  S P Parel; C J Leumann
Journal:  Nucleic Acids Res       Date:  2001-06-01       Impact factor: 16.971

5.  Synthesis and monitored selection of nucleotide surrogates for binding T:A base pairs in homopurine-homopyrimidine DNA triple helices.

Authors:  A A Mokhir; W H Connors; C Richert
Journal:  Nucleic Acids Res       Date:  2001-09-01       Impact factor: 16.971

6.  Cross-linking to an interrupted polypurine sequence with a platinum-modified triplex-forming oligonucleotide.

Authors:  Meghan A Campbell; Paul S Miller
Journal:  J Biol Inorg Chem       Date:  2009-04-07       Impact factor: 3.358

7.  Azole substituted oligonucleotides promote antiparallel triplex formation at non-homopurine duplex targets.

Authors:  R H Durland; T S Rao; V Bodepudi; D M Seth; K Jayaraman; G R Revankar
Journal:  Nucleic Acids Res       Date:  1995-02-25       Impact factor: 16.971

8.  Triple helix formation at (AT)n adjacent to an oligopurine tract.

Authors:  D M Gowers; K R Fox
Journal:  Nucleic Acids Res       Date:  1998-08-15       Impact factor: 16.971

9.  Site-specific targeting of psoralen photoadducts with a triple helix-forming oligonucleotide: characterization of psoralen monoadduct and crosslink formation.

Authors:  F P Gasparro; P A Havre; G A Olack; E J Gunther; P M Glazer
Journal:  Nucleic Acids Res       Date:  1994-07-25       Impact factor: 16.971

10.  Sequence specificity of the non-natural pyrido[2,3-d]pyrimidine nucleoside in triple helix formation.

Authors:  A B Staubli; P B Dervan
Journal:  Nucleic Acids Res       Date:  1994-07-11       Impact factor: 16.971

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