Literature DB >> 16737560

An extra dimension in nucleic acid sequence recognition.

Keith R Fox1, Tom Brown.   

Abstract

Watson-Crick base pairing is a natural molecular recognition process that has been exploited in molecular biology and universally adopted in many fields. An additional mode of nucleic acid sequence recognition that could be used in combination with normal base pairing would add an exta dimension to nucleic acid interactions and open up many new applications. In principle the triplex approach could provide this if developed to recognize any DNA sequence. To this end modified nucleosides have been incorporated into triple-helix-forming oligonucleotides (TFOs) and used to recognize mixed sequence DNA with high selectivity and affinity at neutral pH. Continuing developments are directed towards improving TFO affinity at high pH and increasing triplex association kinetics. A number of applications of triplexes are currently being explored.

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Year:  2006        PMID: 16737560     DOI: 10.1017/S0033583506004197

Source DB:  PubMed          Journal:  Q Rev Biophys        ISSN: 0033-5835            Impact factor:   5.318


  15 in total

1.  Recognition of double-stranded RNA by guanidine-modified peptide nucleic acids.

Authors:  Pankaj Gupta; Oluwatoyosi Muse; Eriks Rozners
Journal:  Biochemistry       Date:  2011-12-20       Impact factor: 3.162

2.  Visualizing the splicing of single pre-mRNA molecules in whole cell extract.

Authors:  Daniel J Crawford; Aaron A Hoskins; Larry J Friedman; Jeff Gelles; Melissa J Moore
Journal:  RNA       Date:  2007-11-19       Impact factor: 4.942

3.  Intramolecular recombination R-triplex in solution: stabilization by bis-intercalator YOYO.

Authors:  Dmitry N Kaluzhny; Vladimir V Timoshin; Olga F Borisova; Victor B Zhurkin; Vladimir L Florentiev; Anna K Shchyolkina
Journal:  J Biomol Struct Dyn       Date:  2008-12

4.  Short peptide nucleic acids bind strongly to homopurine tract of double helical RNA at pH 5.5.

Authors:  Ming Li; Thomas Zengeya; Eriks Rozners
Journal:  J Am Chem Soc       Date:  2010-06-30       Impact factor: 15.419

Review 5.  Oligo/polynucleotide-based gene modification: strategies and therapeutic potential.

Authors:  R Geoffrey Sargent; Soya Kim; Dieter C Gruenert
Journal:  Oligonucleotides       Date:  2011-03-21

6.  Targeting of an interrupted polypurine:polypyrimidine sequence in mammalian cells by a triplex-forming oligonucleotide containing a novel base analogue.

Authors:  A Semenyuk; E Darian; J Liu; A Majumdar; B Cuenoud; P S Miller; A D Mackerell; M M Seidman
Journal:  Biochemistry       Date:  2010-09-14       Impact factor: 3.162

7.  Triple helical recognition of pyrimidine inversions in polypurine tracts of RNA by nucleobase-modified PNA.

Authors:  Pankaj Gupta; Thomas Zengeya; Eriks Rozners
Journal:  Chem Commun (Camb)       Date:  2011-09-12       Impact factor: 6.222

8.  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

9.  Targeted generation of DNA strand breaks using pyrene-conjugated triplex-forming oligonucleotides.

Authors:  Aaron P Benfield; Michael C Macleod; Yaobin Liu; Qi Wu; Theodore G Wensel; Karen M Vasquez
Journal:  Biochemistry       Date:  2008-05-13       Impact factor: 3.162

10.  Selectivity and affinity of DNA triplex forming oligonucleotides containing the nucleoside analogues 2'-O-methyl-5-(3-amino-1-propynyl)uridine and 2'-O-methyl-5-propynyluridine.

Authors:  Hong Li; Paul S Miller; Michael M Seidman
Journal:  Org Biomol Chem       Date:  2008-09-23       Impact factor: 3.876

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