Modification of the aminopyridine unit of 2-deoxyaminopyridinyl-pseudocytidine allowing triplex formation at CG interruptions in homopurine sequences

Lei Wang, Yosuke Taniguchi, Hidenori Okamura, Shigeki Sasaki

Research output: Contribution to journalArticlepeer-review

6 Citations (Scopus)

Abstract

The antigene strategy based on site-specific recognition of duplex DNA by triplex DNA formation has been exploited in a wide range of biological activities. However, specific triplex formation is mostly restricted to homo-purine strands within the target duplex DNA, due to the destabilizing effect of CG and TA inversion sites where there is an absence of natural nucleotides that can recognize the CG and TA base pairs. Hence, the design of artificial nucleosides, which can selectively recognize these inversion sites with high affinity, should be of great significance. Recently, we determined that 2-amino-3-methylpyridinyl pseudo-dC ( 3Me AP-dC) possessed significant affinity and selectivity toward a CG inversion site and showed effective inhibition of gene expression. We now describe the design and synthesis of new modified aminopyridine derivatives by focusing on small chemical modification of the aminopyridine unit to tune and enhance the selectivity and affinity toward CG inversion sites. Remarkably, we have newly found that 2-amino-4-methoxypyridinyl pseudo-dC ( 4OMe AP-dC) could selectively recognize the CG base pair in all four adjacent base pairs and form a stable triplex structure against the promoter sequence of the human gene including multiple CG inversion sites.

Original languageEnglish
Pages (from-to)8679-8688
Number of pages10
JournalNucleic acids research
Volume46
Issue number17
DOIs
Publication statusPublished - 2018

All Science Journal Classification (ASJC) codes

  • Genetics

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