Protected 2'-deoxyribonucleoside triphosphate building blocks for the photocaging of epigenetic 5-(hydroxymethyl)cytosine in DNA
Jazyk angličtina Země Anglie, Velká Británie Médium print
Typ dokumentu časopisecké články, práce podpořená grantem
PubMed
29905748
DOI
10.1039/c8ob01106k
Knihovny.cz E-zdroje
- MeSH
- 5-methylcytosin analogy a deriváty chemická syntéza chemie MeSH
- deoxyribonukleosidy chemická syntéza chemie MeSH
- DNA chemická syntéza chemie MeSH
- fotochemické procesy MeSH
- polyfosfáty chemická syntéza chemie MeSH
- světlo MeSH
- ultrafialové záření MeSH
- Publikační typ
- časopisecké články MeSH
- práce podpořená grantem MeSH
- Názvy látek
- 5-hydroxymethylcytosine MeSH Prohlížeč
- 5-methylcytosin MeSH
- deoxyribonukleosidy MeSH
- DNA MeSH
- polyfosfáty MeSH
- triphosphoric acid MeSH Prohlížeč
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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