Hydrogen peroxide-triggered gene silencing in mammalian cells through boronated antisense oligonucleotides.
Shohei MoriKunihiko MorihiroTakumi OkudaYuuya KasaharaSatoshi ObikaPublished in: Chemical science (2017)
Hydrogen peroxide (H2O2) is a reactive oxygen species (ROS) involved in various diseases, including neurodegeneration, diabetes, and cancer. Here, we introduce a new approach to use H2O2 to modulate specific gene expression in mammalian cells. H2O2-responsive nucleoside analogues, in which the Watson-Crick faces of the nucleobases are caged by arylboronate moieties, were synthesized. One of these analogues, boronated thymidine (dTB ), was incorporated into oligodeoxynucleotides (ODNs) using an automated DNA synthesizer. The hybridization ability of this boronated ODN to complementary RNA was clearly switched in the off-to-on direction upon H2O2 addition. Furthermore, we demonstrated H2O2-triggered gene silencing in mammalian cells using antisense oligonucleotides (ASOs) modified with dTB . Our approach can be used for the regulation of any gene of interest by the sequence design of boronated ASOs and will contribute to the development of targeted disease therapeutics.
Keyphrases
- hydrogen peroxide
- nucleic acid
- reactive oxygen species
- gene expression
- nitric oxide
- molecular docking
- cancer therapy
- type diabetes
- papillary thyroid
- dna methylation
- cardiovascular disease
- small molecule
- cell death
- genome wide
- structure activity relationship
- copy number
- squamous cell
- single molecule
- squamous cell carcinoma
- oxidative stress
- amino acid
- adipose tissue
- molecular dynamics simulations
- oxide nanoparticles