Deterioration of RNA Study

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The current status of the problem
The chemical modification in triplex forming oligonucleotides affects the stability of RNA triplex. The incorporation of 2-omethayl-modify residues in a triplex forming oligonucleotides destabilizes and stabilizes triplex formation with RNA and DNA duplex regions (Patterson, Plaxco & Ricci, 2010). The deterioration of RNA triplex formation may be making easy through modulation of van der Waals contact, base stacking backbone pre-organization, geometric compatibility and dehydration energy (Patterson, Plaxco & Ricci, 2010).
Antisense are frequently very large numbers of mRNA molecules in a cell, and it is hard to attain complete inhibition of a specific mRNA. On top of that, the feedback mechanisms exist that can lead to enlarged mRNA production, in response to obliteration of mRNA in antisense therapy. It is shown that parallel triplexes are thermodynamically less stable at physiological pH (Patterson, Plaxco & Ricci, 2010). Two reasons for the instability of triplexes at pH 7 and above include, the C+·GC triplet is stabilized by prolongation which only occurs at low pH and the juxtaposition of three polyanionic DNA strands is destabilizing at all pH values (Patterson, Plaxco & Ricci, 2010).
Another problem is that the Triplex-directed DNA recognition is strictly limited by polyp urine sequence, the recognition of base pair inversions, in a duplex by chimeric TFOs, containing α-thymidine and α-deoxyguanosine (Patterson, Plaxco & Ricci, 2010). The hybridization of hairpin with an array of chimeric probes proposes that recognition of double-stranded DNA follows complex rules combining reversed Hoogsteen and non-canonical homologous hydrogen bonding.
Molecules that bind to the DNA double helix may i...

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...chemistry, 82(21), 9109-9115.
Reason for use: It describes the development of therapeutics and functional genomics applications) Besch, R., & Degitz, K, 2004, Triplex-forming oligonucleotides-sequence- specific DNA ligands as tools for gene inhibition and for modulation of DNA-associated functions. Current drug targets, 5(8), 691-703.
(Reason for use: Explains the status of transcription activity on efficiency of triplex formation and binding and antigene activity of a daunomycin-conjugated triplex-forming oligonucleotid)
Guntaka, R. V., & Weber, K. T, 2003, Triplex-forming oligonucleotides as modulators of gene expression. The international journal of biochemistry & cell biology, 35(1), 22-31.
(Reason for use: Forms the basis of the scientific disciplines of molecular biology and genetics and underpinsgenomics, DNA diagnostics and modern aspects of forensic science)

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