| Literature DB >> 26708259 |
Y Pavan Kumar1, Puja Saha1, Dhurjhoti Saha2, Irene Bessi3, Harald Schwalbe3, Shantanu Chowdhury2, Jyotirmayee Dash4.
Abstract
The four-stranded G-quadruplex present in the c-MYC P1 promoter has been shown to play a pivotal role in the regulation of c-MYC transcription. Small-molecule compounds capable of inhibiting the c-MYC promoter activity by stabilising the c-MYC G-quadruplex could potentially be used as anticancer agents. In this context, here we report the synthesis of dansyl-guanosine conjugates through one-pot modular click reactions. The dansyl-guanosine conjugates can selectively detect c-MYC G-quadruplex over other biologically relevant quadruplexes and duplex DNA and can be useful as staining reagents for selective visualisation of c-MYC G-quadruplex over duplex DNA by gel electrophoresis. NMR spectroscopic titrations revealed the preferential binding sites of these dansyl ligands to the c-MYC G-quadruplex. A dual luciferase assay and qRT-PCR revealed that a dansyl-bisguanosine ligand represses the c-MYC expression, possibly by stabilising the c-MYC G-quadruplex.Entities:
Keywords: G-quadruplexes; NMR spectroscopy; click chemistry; fluorescent probes; gel electrophoresis; transcription
Mesh:
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Year: 2016 PMID: 26708259 DOI: 10.1002/cbic.201500631
Source DB: PubMed Journal: Chembiochem ISSN: 1439-4227 Impact factor: 3.164