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Modified Nucleotides for Discrimination between Cytosine and the Epigenetic Marker 5‐Methylcytosine

5‐Methyl‐2′‐deoxycytosine, the most common epigenetic marker of DNA in eukaryotic cells, plays a key role in gene regulation and affects various cellular processes such as development and carcinogenesis. Therefore, the detection of 5mC can serve as an important biomarker for diagnostics. Here we des...

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Detalles Bibliográficos
Autores principales: von Watzdorf, Janina, Leitner, Kim, Marx, Andreas
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4949677/
https://www.ncbi.nlm.nih.gov/pubmed/26835661
http://dx.doi.org/10.1002/anie.201511520
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author von Watzdorf, Janina
Leitner, Kim
Marx, Andreas
author_facet von Watzdorf, Janina
Leitner, Kim
Marx, Andreas
author_sort von Watzdorf, Janina
collection PubMed
description 5‐Methyl‐2′‐deoxycytosine, the most common epigenetic marker of DNA in eukaryotic cells, plays a key role in gene regulation and affects various cellular processes such as development and carcinogenesis. Therefore, the detection of 5mC can serve as an important biomarker for diagnostics. Here we describe that modified dGTP analogues as well as modified primers are able to sense the presence or absence of a single methylation of C, even though this modification does not interfere directly with Watson–Crick nucleobase pairing. By screening several modified nucleotide scaffolds, O(6)‐modified 2′‐deoxyguanosine analogues were identified as discriminating between C and 5mC. These modified nucleotides might find application in site‐specific 5mC detection, for example, through real‐time PCR approaches.
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spelling pubmed-49496772016-07-28 Modified Nucleotides for Discrimination between Cytosine and the Epigenetic Marker 5‐Methylcytosine von Watzdorf, Janina Leitner, Kim Marx, Andreas Angew Chem Int Ed Engl Communications 5‐Methyl‐2′‐deoxycytosine, the most common epigenetic marker of DNA in eukaryotic cells, plays a key role in gene regulation and affects various cellular processes such as development and carcinogenesis. Therefore, the detection of 5mC can serve as an important biomarker for diagnostics. Here we describe that modified dGTP analogues as well as modified primers are able to sense the presence or absence of a single methylation of C, even though this modification does not interfere directly with Watson–Crick nucleobase pairing. By screening several modified nucleotide scaffolds, O(6)‐modified 2′‐deoxyguanosine analogues were identified as discriminating between C and 5mC. These modified nucleotides might find application in site‐specific 5mC detection, for example, through real‐time PCR approaches. John Wiley and Sons Inc. 2016-02-02 2016-02-24 /pmc/articles/PMC4949677/ /pubmed/26835661 http://dx.doi.org/10.1002/anie.201511520 Text en © 2016 The Authors. Published by Wiley-VCH Verlag GmbH & Co. KGaA. This is an open access article under the terms of the Creative Commons Attribution (http://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Communications
von Watzdorf, Janina
Leitner, Kim
Marx, Andreas
Modified Nucleotides for Discrimination between Cytosine and the Epigenetic Marker 5‐Methylcytosine
title Modified Nucleotides for Discrimination between Cytosine and the Epigenetic Marker 5‐Methylcytosine
title_full Modified Nucleotides for Discrimination between Cytosine and the Epigenetic Marker 5‐Methylcytosine
title_fullStr Modified Nucleotides for Discrimination between Cytosine and the Epigenetic Marker 5‐Methylcytosine
title_full_unstemmed Modified Nucleotides for Discrimination between Cytosine and the Epigenetic Marker 5‐Methylcytosine
title_short Modified Nucleotides for Discrimination between Cytosine and the Epigenetic Marker 5‐Methylcytosine
title_sort modified nucleotides for discrimination between cytosine and the epigenetic marker 5‐methylcytosine
topic Communications
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4949677/
https://www.ncbi.nlm.nih.gov/pubmed/26835661
http://dx.doi.org/10.1002/anie.201511520
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