Protected 2'-deoxyribonucleoside triphosphate building blocks for the photocaging of epigenetic 5-(hydroxymethyl)cytosine in DNA
Language English Country England, Great Britain Media print
Document type Journal Article, Research Support, Non-U.S. Gov't
PubMed
29905748
DOI
10.1039/c8ob01106k
Knihovny.cz E-resources
- MeSH
- 5-Methylcytosine analogs & derivatives chemical synthesis chemistry MeSH
- Deoxyribonucleosides chemical synthesis chemistry MeSH
- DNA chemical synthesis chemistry MeSH
- Photochemical Processes MeSH
- Polyphosphates chemical synthesis chemistry MeSH
- Light MeSH
- Ultraviolet Rays MeSH
- Publication type
- Journal Article MeSH
- Research Support, Non-U.S. Gov't MeSH
- Names of Substances
- 5-hydroxymethylcytosine MeSH Browser
- 5-Methylcytosine MeSH
- Deoxyribonucleosides MeSH
- DNA MeSH
- Polyphosphates MeSH
- triphosphoric acid MeSH Browser
2'-Deoxyribonucleoside triphosphates (dNTPs) containing 5-(hydroxymethyl)cytosine (5hmC) protected with photocleavable groups (2-nitrobenzyl or 6-nitropiperonyl) were prepared and studied as substrates for the enzymatic synthesis of oligonucleotides and DNA containing a photocaged epigenetic 5hmC base. DNA probes containing photocaged or free 5hmC in the recognition sequence of restriction endonucleases were prepared and used for the study of the photorelease of caged DNA by UV or visible light at different wavelengths. The nitrobenzyl-protected dNTP was a slightly better substrate for DNA polymerases in primer extension or PCR, whereas the nitropiperonyl-protected nucleotide underwent slightly faster photorelease at 400 nm. However, both photocaged building blocks can be used in polymerase synthesis and the photorelease of 5hmC in DNA.
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