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Genome-wide mapping of 5-hydroxymethyluracil in the eukaryote parasite Leishmania

BACKGROUND: 5-Hydroxymethyluracil (5hmU) is a thymine base modification found in the genomes of a diverse range of organisms. To explore the functional importance of 5hmU, we develop a method for the genome-wide mapping of 5hmU-modified loci based on a chemical tagging strategy for the hydroxymethyl...

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Autores principales: Kawasaki, Fumiko, Beraldi, Dario, Hardisty, Robyn E., McInroy, Gordon R., van Delft, Pieter, Balasubramanian, Shankar
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5282726/
https://www.ncbi.nlm.nih.gov/pubmed/28137275
http://dx.doi.org/10.1186/s13059-017-1150-1
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author Kawasaki, Fumiko
Beraldi, Dario
Hardisty, Robyn E.
McInroy, Gordon R.
van Delft, Pieter
Balasubramanian, Shankar
author_facet Kawasaki, Fumiko
Beraldi, Dario
Hardisty, Robyn E.
McInroy, Gordon R.
van Delft, Pieter
Balasubramanian, Shankar
author_sort Kawasaki, Fumiko
collection PubMed
description BACKGROUND: 5-Hydroxymethyluracil (5hmU) is a thymine base modification found in the genomes of a diverse range of organisms. To explore the functional importance of 5hmU, we develop a method for the genome-wide mapping of 5hmU-modified loci based on a chemical tagging strategy for the hydroxymethyl group. RESULTS: We apply the method to generate genome-wide maps of 5hmU in the parasitic protozoan Leishmania sp. In this genus, another thymine modification, 5-(β-glucopyranosyl) hydroxymethyluracil (base J), plays a key role during transcription. To elucidate the relationship between 5hmU and base J, we also map base J loci by introducing a chemical tagging strategy for the glucopyranoside residue. Observed 5hmU peaks are highly consistent among technical replicates, confirming the robustness of the method. 5hmU is enriched in strand switch regions, telomeric regions, and intergenic regions. Over 90% of 5hmU-enriched loci overlapped with base J-enriched loci, which occurs mostly within strand switch regions. We also identify loci comprising 5hmU but not base J, which are enriched with motifs consisting of a stretch of thymine bases. CONCLUSIONS: By chemically detecting 5hmU we present a method to provide a genome-wide map of this modification, which will help address the emerging interest in the role of 5hmU. This method will also be applicable to other organisms bearing 5hmU. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s13059-017-1150-1) contains supplementary material, which is available to authorized users.
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spelling pubmed-52827262017-02-03 Genome-wide mapping of 5-hydroxymethyluracil in the eukaryote parasite Leishmania Kawasaki, Fumiko Beraldi, Dario Hardisty, Robyn E. McInroy, Gordon R. van Delft, Pieter Balasubramanian, Shankar Genome Biol Research BACKGROUND: 5-Hydroxymethyluracil (5hmU) is a thymine base modification found in the genomes of a diverse range of organisms. To explore the functional importance of 5hmU, we develop a method for the genome-wide mapping of 5hmU-modified loci based on a chemical tagging strategy for the hydroxymethyl group. RESULTS: We apply the method to generate genome-wide maps of 5hmU in the parasitic protozoan Leishmania sp. In this genus, another thymine modification, 5-(β-glucopyranosyl) hydroxymethyluracil (base J), plays a key role during transcription. To elucidate the relationship between 5hmU and base J, we also map base J loci by introducing a chemical tagging strategy for the glucopyranoside residue. Observed 5hmU peaks are highly consistent among technical replicates, confirming the robustness of the method. 5hmU is enriched in strand switch regions, telomeric regions, and intergenic regions. Over 90% of 5hmU-enriched loci overlapped with base J-enriched loci, which occurs mostly within strand switch regions. We also identify loci comprising 5hmU but not base J, which are enriched with motifs consisting of a stretch of thymine bases. CONCLUSIONS: By chemically detecting 5hmU we present a method to provide a genome-wide map of this modification, which will help address the emerging interest in the role of 5hmU. This method will also be applicable to other organisms bearing 5hmU. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s13059-017-1150-1) contains supplementary material, which is available to authorized users. BioMed Central 2017-01-30 /pmc/articles/PMC5282726/ /pubmed/28137275 http://dx.doi.org/10.1186/s13059-017-1150-1 Text en © The Author(s). 2017 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research
Kawasaki, Fumiko
Beraldi, Dario
Hardisty, Robyn E.
McInroy, Gordon R.
van Delft, Pieter
Balasubramanian, Shankar
Genome-wide mapping of 5-hydroxymethyluracil in the eukaryote parasite Leishmania
title Genome-wide mapping of 5-hydroxymethyluracil in the eukaryote parasite Leishmania
title_full Genome-wide mapping of 5-hydroxymethyluracil in the eukaryote parasite Leishmania
title_fullStr Genome-wide mapping of 5-hydroxymethyluracil in the eukaryote parasite Leishmania
title_full_unstemmed Genome-wide mapping of 5-hydroxymethyluracil in the eukaryote parasite Leishmania
title_short Genome-wide mapping of 5-hydroxymethyluracil in the eukaryote parasite Leishmania
title_sort genome-wide mapping of 5-hydroxymethyluracil in the eukaryote parasite leishmania
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5282726/
https://www.ncbi.nlm.nih.gov/pubmed/28137275
http://dx.doi.org/10.1186/s13059-017-1150-1
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