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Detection of Genomic Uracil Patterns

The appearance of uracil in the deoxyuridine moiety of DNA is among the most frequently occurring genomic modifications. Three different routes can result in genomic uracil, two of which do not require specific enzymes: spontaneous cytosine deamination due to the inherent chemical reactivity of livi...

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Autores principales: Békési, Angéla, Holub, Eszter, Pálinkás, Hajnalka Laura, Vértessy, Beáta G.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8070346/
https://www.ncbi.nlm.nih.gov/pubmed/33918885
http://dx.doi.org/10.3390/ijms22083902
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author Békési, Angéla
Holub, Eszter
Pálinkás, Hajnalka Laura
Vértessy, Beáta G.
author_facet Békési, Angéla
Holub, Eszter
Pálinkás, Hajnalka Laura
Vértessy, Beáta G.
author_sort Békési, Angéla
collection PubMed
description The appearance of uracil in the deoxyuridine moiety of DNA is among the most frequently occurring genomic modifications. Three different routes can result in genomic uracil, two of which do not require specific enzymes: spontaneous cytosine deamination due to the inherent chemical reactivity of living cells, and thymine-replacing incorporation upon nucleotide pool imbalances. There is also an enzymatic pathway of cytosine deamination with multiple DNA (cytosine) deaminases involved in this process. In order to describe potential roles of genomic uracil, it is of key importance to utilize efficient uracil-DNA detection methods. In this review, we provide a comprehensive and critical assessment of currently available uracil detection methods with special focus on genome-wide mapping solutions. Recent developments in PCR-based and in situ detection as well as the quantitation of genomic uracil are also discussed.
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spelling pubmed-80703462021-04-26 Detection of Genomic Uracil Patterns Békési, Angéla Holub, Eszter Pálinkás, Hajnalka Laura Vértessy, Beáta G. Int J Mol Sci Review The appearance of uracil in the deoxyuridine moiety of DNA is among the most frequently occurring genomic modifications. Three different routes can result in genomic uracil, two of which do not require specific enzymes: spontaneous cytosine deamination due to the inherent chemical reactivity of living cells, and thymine-replacing incorporation upon nucleotide pool imbalances. There is also an enzymatic pathway of cytosine deamination with multiple DNA (cytosine) deaminases involved in this process. In order to describe potential roles of genomic uracil, it is of key importance to utilize efficient uracil-DNA detection methods. In this review, we provide a comprehensive and critical assessment of currently available uracil detection methods with special focus on genome-wide mapping solutions. Recent developments in PCR-based and in situ detection as well as the quantitation of genomic uracil are also discussed. MDPI 2021-04-09 /pmc/articles/PMC8070346/ /pubmed/33918885 http://dx.doi.org/10.3390/ijms22083902 Text en © 2021 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Review
Békési, Angéla
Holub, Eszter
Pálinkás, Hajnalka Laura
Vértessy, Beáta G.
Detection of Genomic Uracil Patterns
title Detection of Genomic Uracil Patterns
title_full Detection of Genomic Uracil Patterns
title_fullStr Detection of Genomic Uracil Patterns
title_full_unstemmed Detection of Genomic Uracil Patterns
title_short Detection of Genomic Uracil Patterns
title_sort detection of genomic uracil patterns
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8070346/
https://www.ncbi.nlm.nih.gov/pubmed/33918885
http://dx.doi.org/10.3390/ijms22083902
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