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Evaluation of N(6)-methyldeoxyadenosine antibody-based genomic profiling in eukaryotes

Low-level DNA N(6)-methyldeoxyadenosine (DNA-m6A) has recently been reported across various eukaryotes. Although anti-m6A antibody–based approaches are commonly used to measure DNA-m6A levels, this approach is known to be confounded by DNA secondary structures, RNA contamination, and bacterial conta...

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Detalles Bibliográficos
Autores principales: Debo, Brian M., Mallory, Benjamin J., Stergachis, Andrew B.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cold Spring Harbor Laboratory Press 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10078290/
https://www.ncbi.nlm.nih.gov/pubmed/36788024
http://dx.doi.org/10.1101/gr.276696.122
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author Debo, Brian M.
Mallory, Benjamin J.
Stergachis, Andrew B.
author_facet Debo, Brian M.
Mallory, Benjamin J.
Stergachis, Andrew B.
author_sort Debo, Brian M.
collection PubMed
description Low-level DNA N(6)-methyldeoxyadenosine (DNA-m6A) has recently been reported across various eukaryotes. Although anti-m6A antibody–based approaches are commonly used to measure DNA-m6A levels, this approach is known to be confounded by DNA secondary structures, RNA contamination, and bacterial contamination. To evaluate for these confounding features, we introduce an approach for systematically validating the selectivity of antibody-based DNA-m6A methods and use a highly selective anti-DNA-m6A antibody to reexamine patterns of DNA-m6A in C. reinhardtii, A. thaliana, and D. melanogaster. Our findings raise caution about the use of antibody-based methods for endogenous m6A quantification and mapping in eukaryotes.
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spelling pubmed-100782902023-09-01 Evaluation of N(6)-methyldeoxyadenosine antibody-based genomic profiling in eukaryotes Debo, Brian M. Mallory, Benjamin J. Stergachis, Andrew B. Genome Res Methods Low-level DNA N(6)-methyldeoxyadenosine (DNA-m6A) has recently been reported across various eukaryotes. Although anti-m6A antibody–based approaches are commonly used to measure DNA-m6A levels, this approach is known to be confounded by DNA secondary structures, RNA contamination, and bacterial contamination. To evaluate for these confounding features, we introduce an approach for systematically validating the selectivity of antibody-based DNA-m6A methods and use a highly selective anti-DNA-m6A antibody to reexamine patterns of DNA-m6A in C. reinhardtii, A. thaliana, and D. melanogaster. Our findings raise caution about the use of antibody-based methods for endogenous m6A quantification and mapping in eukaryotes. Cold Spring Harbor Laboratory Press 2023-03 /pmc/articles/PMC10078290/ /pubmed/36788024 http://dx.doi.org/10.1101/gr.276696.122 Text en © 2023 Debo et al.; Published by Cold Spring Harbor Laboratory Press https://creativecommons.org/licenses/by-nc/4.0/This article is distributed exclusively by Cold Spring Harbor Laboratory Press for the first six months after the full-issue publication date (see https://genome.cshlp.org/site/misc/terms.xhtml). After six months, it is available under a Creative Commons License (Attribution-NonCommercial 4.0 International), as described at http://creativecommons.org/licenses/by-nc/4.0/ (https://creativecommons.org/licenses/by-nc/4.0/) .
spellingShingle Methods
Debo, Brian M.
Mallory, Benjamin J.
Stergachis, Andrew B.
Evaluation of N(6)-methyldeoxyadenosine antibody-based genomic profiling in eukaryotes
title Evaluation of N(6)-methyldeoxyadenosine antibody-based genomic profiling in eukaryotes
title_full Evaluation of N(6)-methyldeoxyadenosine antibody-based genomic profiling in eukaryotes
title_fullStr Evaluation of N(6)-methyldeoxyadenosine antibody-based genomic profiling in eukaryotes
title_full_unstemmed Evaluation of N(6)-methyldeoxyadenosine antibody-based genomic profiling in eukaryotes
title_short Evaluation of N(6)-methyldeoxyadenosine antibody-based genomic profiling in eukaryotes
title_sort evaluation of n(6)-methyldeoxyadenosine antibody-based genomic profiling in eukaryotes
topic Methods
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10078290/
https://www.ncbi.nlm.nih.gov/pubmed/36788024
http://dx.doi.org/10.1101/gr.276696.122
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