Literature DB >> 9427655

Beyond guanine quartets: cation-induced formation of homogenous and chimeric DNA tetraplexes incorporating iso-guanine and guanine.

C Roberts1, J C Chaput, C Switzer.   

Abstract

BACKGROUND: iso-Guanine (iso-G) is the purine component of an isomeric Watson-Crick base pair that may have existed prebiotically. By comparing the abiotic molecular recognition properties of iso-G and its complement, iso-cytosine (iso-C), with those of genomic nucleotide bases, it may be possible to explain the exclusion of the iso-G-iso-C base pair from modern genomes. Whether a nucleobase forms quartets may have a key role in determining its functionality. Biotically, nucleic acid tetraplexes have been implicated in cellular functions; prebiotically, tetraplexes would probably interfere with replication. Recently, in vitro selection has yielded receptors and catalysts that incorporate G quartets. The versatility of these structures could be enhanced by expanding the range of bases that can form the quartet motif.
RESULTS: Native polyacrylamide gel electrophoresis of oligonucleotides bearing runs of iso-G provides strong support for tetraplex formation via cation-promoted DNA strand association. In particular, when strands of different lengths bearing the same iso-G tetrad recognition element were combined, five bands were observed after electrophoresis, corresponding to all possible heterotetraplexes with parallel strand alignment. An analogous experiment with a mixture of strands bearing iso-G or G tetrad recognition domains supports the existence of mixed iso-G/G tetraplexes with antiparallel strand alignment at chimeric junctions. iso-G tetraplex and quartet structure has also been probed by a photo-crosslinking experiment, ultra-violet spectroscopy and theoretical calculations.
CONCLUSIONS: As iso-G and G both have a marked tendency to form tetraplexes, their tandem inclusion in genetic material may be problematic, leading to double-stranded DNA half composed of bases that have a tendency to auto-associate. The resulting density of 'selfish' bases could undermine Watson-Crick pair formation, especially in a prebiotic context devoid of enzymes. Nevertheless, the ability of iso-G to form mixed quartets with G may provide a basis for altering the properties of tetraplexes in the domain of artificial receptors or catalysts from in vitro selections.

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Year:  1997        PMID: 9427655     DOI: 10.1016/s1074-5521(97)90298-2

Source DB:  PubMed          Journal:  Chem Biol        ISSN: 1074-5521


  7 in total

1.  A DNA pentaplex incorporating nucleobase quintets.

Authors:  J C Chaput; C Switzer
Journal:  Proc Natl Acad Sci U S A       Date:  1999-09-14       Impact factor: 11.205

Review 2.  In What Ways Do Synthetic Nucleotides and Natural Base Lesions Alter the Structural Stability of G-Quadruplex Nucleic Acids?

Authors:  Janos Sagi
Journal:  J Nucleic Acids       Date:  2017-10-18

3.  Structural studies of a stable parallel-stranded DNA duplex incorporating isoguanine:cytosine and isocytosine:guanine basepairs by nuclear magnetic resonance spectroscopy.

Authors:  X L Yang; H Sugiyama; S Ikeda; I Saito; A H Wang
Journal:  Biophys J       Date:  1998-09       Impact factor: 4.033

4.  Guanine-centric self-assembly of nucleotides in water: an important consideration in prebiotic chemistry.

Authors:  Lauren M Cassidy; Bradley T Burcar; Wyatt Stevens; Elizabeth M Moriarty; Linda B McGown
Journal:  Astrobiology       Date:  2014-10-06       Impact factor: 4.335

5.  Examination of the effect of the annealing cation on higher order structures containing guanine or isoguanine repeats.

Authors:  Sarah E Pierce; Junmei Wang; Janarthanan Jayawickramarajah; Andrew D Hamilton; Jennifer S Brodbelt
Journal:  Chemistry       Date:  2009-10-26       Impact factor: 5.236

6.  Novel isoguanine derivative of unlocked nucleic acid-Investigations of thermodynamics and biological potential of modified thrombin binding aptamer.

Authors:  Weronika Kotkowiak; Tomasz Czapik; Anna Pasternak
Journal:  PLoS One       Date:  2018-05-24       Impact factor: 3.240

7.  Substituted adenine quartets: interplay between substituent effect, hydrogen bonding, and aromaticity.

Authors:  Halina Szatylowicz; Paulina H Marek; Olga A Stasyuk; Tadeusz M Krygowski; Miquel Solà
Journal:  RSC Adv       Date:  2020-06-18       Impact factor: 4.036

  7 in total

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