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Steigenberger, B., Schiesser, S., Hackner, B., Brandmayr, C., Laube, S.K., Steinbacher, J., Pfaffeneder, T. and Carell, T. (2013) Synthesis of 5-Hydroxymethyl-, 5-Formyl-, and 5-Carboxycytidine-Triphosphates and Their Incorporation into Oligonucleotides by Polymerase Chain Reaction. Organic Letters, 15, 366-369.
https://doi.org/10.1021/ol3033219

has been cited by the following article:

• TITLE: DNA-Like Duplex Structures Derived from Chemistry Based on 2’-Deoxy-Cytidine: A New Model for Base-Specific Inhibition of G and C on DNA and RNA Level

  AUTHORS: Henk M. Buck

  KEYWORDS: Active Demethylation, DNA Catalysis, Symmetry Elements, (Anti)Parallel Modified DNA and RNA, Inhibition of Genetic Information

  JOURNAL NAME: Journal of Biophysical Chemistry, Vol.9 No.3, December 29, 2018

  ABSTRACT: The new epigenetic elements 5-hydroxymethyl-dC, 5-formyl-dC, and 5-car- boxy-dC may be considered as intermediates of an active demethylation process. A comprehensive mechanistic model is given for the C-C bond cleavage focused on the chemistry within the DNA duplex structure. In addition we register spin-off chemistry of this process in evaluating new duplex systems closely related to natural DNA and RNA concerning their hydrogen-bond symmetrization. A model is composed for a base-specific inhibition of G and C on the DNA and RNA level. C-G combinations are of general importance in controlling the dynamics of gene expression. In some way the suggested model systems are related to antisense oligonucleotides (ASOs).