Literature DB >> 9115352

Strong, specific, monodentate G-C base pair recognition by N7-inosine derivatives in the pyrimidine.purine-pyrimidine triple-helical binding motif.

J Marfurt1, S P Parel, C J Leumann.   

Abstract

The nucleoside analogs 7-(2'-deoxy-alpha-D-ribofuranosyl)hypoxanthine (alpha7H,1), 7-(2'-deoxy-beta-D-ribofuranosyl)hypoxanthine (beta7H,2) and 7-7-(2'-O-methyl-beta-D- ribofuranosyl)hypoxanthine (beta7HOMe,3) were prepared and incorporated into triplex forming oligodeoxynucleotides, designed to bind to DNA in the parallel (pyrimidine.purine-pyrimidine) motif. By DNase I footprinting techniques and UV-melting curve analysis it was found that, at pH 7. 0, the 15mer oligonucleotides d(TTTTTMeCTXTMeCTMeCTMeCT) (MeC = 5-methyl-deoxycytidine, X =beta7H,beta7HOMe) bind to a DNA target duplex forming a H.G-C base triple with equal to slightly increased (10-fold) stability compared to a control oligodeoxynucleotide in which the hypoxanthine residue is replaced by MeC. Remarkably, triple-helix formation is specific to G-C base pairs and up to 40 microM third strand concentration, no stable triplex exhibiting H.A-T, H.T-A or H.C-G base arrangements could be found (target duplex concentration approximately 0.1 nM). Multiply substituted sequences containing beta7H residues either in an isolated [d(TTTTTbeta7HTbeta7HTbeta7HTbeta7HTbeta7HT)] or in a contiguous [d(TTTbeta7Hbeta7Hbeta7Hbeta7HTTTTbeta7HTTT)] manner still form triplexes with their targets of comparable stability as the control (MeC-containing) sequences at pH 7.0 and high salt or spermine containing buffers. General considerations lead to a structural model in which the recognition of the G-C base pair by hypoxanthine takes place via only one H-bond of the N-H of hypoxanthine to N7 of guanine. This model is supported by a molecular dynamics simulation. A general comparison of the triplex forming properties of oligonucleotides containing beta7H with those containing MeC or N7-2'-deoxyguanosine (N7G) reveals that monodentate recognition in the former case can energetically compete with bidentate recognition in the latter two cases.

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Year:  1997        PMID: 9115352      PMCID: PMC146675          DOI: 10.1093/nar/25.10.1875

Source DB:  PubMed          Journal:  Nucleic Acids Res        ISSN: 0305-1048            Impact factor:   16.971


  19 in total

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2.  Second structural motif for recognition of DNA by oligonucleotide-directed triple-helix formation.

Authors:  P A Beal; P B Dervan
Journal:  Science       Date:  1991-03-15       Impact factor: 47.728

3.  Efficient triple helix formation by oligodeoxyribonucleotides containing alpha- or beta-2-amino-5-(2-deoxy-D-ribofuranosyl) pyridine residues.

Authors:  P J Bates; C A Laughton; T C Jenkins; D C Capaldi; P D Roselt; C B Reese; S Neidle
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4.  DNA triplex formation of oligonucleotide analogues consisting of linker groups and octamer segments that have opposite sugar-phosphate backbone polarities.

Authors:  A Ono; C N Chen; L S Kan
Journal:  Biochemistry       Date:  1991-10-15       Impact factor: 3.162

5.  Sequence-specific cleavage of double helical DNA by triple helix formation.

Authors:  H E Moser; P B Dervan
Journal:  Science       Date:  1987-10-30       Impact factor: 47.728

6.  Recognition of thymine adenine.base pairs by guanine in a pyrimidine triple helix motif.

Authors:  L C Griffin; P B Dervan
Journal:  Science       Date:  1989-09-01       Impact factor: 47.728

7.  Structures for the polynucleotide complexes poly(dA) with poly (dT) and poly(dT) with poly(dA) with poly (dT).

Authors:  S Arnott; E Selsing
Journal:  J Mol Biol       Date:  1974-09-15       Impact factor: 5.469

8.  Purine nucleosides. XX. The synthesis of 7-beta-D-ribofuranosylpurines from imidazole nucleoside derivatives.

Authors:  R J Rousseau; R K Robins; L B Townsend
Journal:  J Am Chem Soc       Date:  1968-05-08       Impact factor: 15.419

9.  Binding of triple helix forming oligonucleotides to sites in gene promoters.

Authors:  R H Durland; D J Kessler; S Gunnell; M Duvic; B M Pettitt; M E Hogan
Journal:  Biochemistry       Date:  1991-09-24       Impact factor: 3.162

10.  Sequence-specific recognition of the major groove of DNA by oligodeoxynucleotides via triple helix formation. Footprinting studies.

Authors:  J C François; T Saison-Behmoaras; C Hélène
Journal:  Nucleic Acids Res       Date:  1988-12-23       Impact factor: 16.971

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  2 in total

Review 1.  Unnatural bases for recognition of noncoding nucleic acid interfaces.

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Journal:  Biopolymers       Date:  2020-09-24       Impact factor: 2.505

2.  Structural properties and gene-silencing activity of chemically modified DNA-RNA hybrids with parallel orientation.

Authors:  Maryam Habibian; Maryam Yahyaee-Anzahaee; Matije Lucic; Elena Moroz; Nerea Martín-Pintado; Logan Dante Di Giovanni; Jean-Christophe Leroux; Jonathan Hall; Carlos González; Masad J Damha
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