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Genome-wide profiling of histone modifications in Plasmodium falciparum using CUT&RUN

We recently adapted a CUT&RUN protocol for genome-wide profiling of chromatin modifications in the human malaria parasite Plasmodium. Using the step-by-step protocol described below, we were able to generate high-quality profiles of multiple histone modifications using only a small fraction of t...

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Autores principales: Morillo, Riward Campelo, Harris, Chantal T, Kennedy, Kit, Henning, Samuel R, Kafsack, Björn FC
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Life Science Alliance LLC 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9670794/
https://www.ncbi.nlm.nih.gov/pubmed/36379668
http://dx.doi.org/10.26508/lsa.202201778
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author Morillo, Riward Campelo
Harris, Chantal T
Kennedy, Kit
Henning, Samuel R
Kafsack, Björn FC
author_facet Morillo, Riward Campelo
Harris, Chantal T
Kennedy, Kit
Henning, Samuel R
Kafsack, Björn FC
author_sort Morillo, Riward Campelo
collection PubMed
description We recently adapted a CUT&RUN protocol for genome-wide profiling of chromatin modifications in the human malaria parasite Plasmodium. Using the step-by-step protocol described below, we were able to generate high-quality profiles of multiple histone modifications using only a small fraction of the cells required for ChIP-seq. Using antibodies against two commonly profiled histone modifications, H3K4me3 and H3K9me3, we show here that CUT&RUN profiling is highly reproducible and closely recapitulates previously published ChIP-seq-based abundance profiles of histone marks. Finally, we show that CUT&RUN requires substantially lower sequencing coverage for accurate profiling compared with ChIP-seq.
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spelling pubmed-96707942022-11-18 Genome-wide profiling of histone modifications in Plasmodium falciparum using CUT&RUN Morillo, Riward Campelo Harris, Chantal T Kennedy, Kit Henning, Samuel R Kafsack, Björn FC Life Sci Alliance Methods We recently adapted a CUT&RUN protocol for genome-wide profiling of chromatin modifications in the human malaria parasite Plasmodium. Using the step-by-step protocol described below, we were able to generate high-quality profiles of multiple histone modifications using only a small fraction of the cells required for ChIP-seq. Using antibodies against two commonly profiled histone modifications, H3K4me3 and H3K9me3, we show here that CUT&RUN profiling is highly reproducible and closely recapitulates previously published ChIP-seq-based abundance profiles of histone marks. Finally, we show that CUT&RUN requires substantially lower sequencing coverage for accurate profiling compared with ChIP-seq. Life Science Alliance LLC 2022-11-15 /pmc/articles/PMC9670794/ /pubmed/36379668 http://dx.doi.org/10.26508/lsa.202201778 Text en © 2022 Morillo et al. https://creativecommons.org/licenses/by/4.0/This article is available under a Creative Commons License (Attribution 4.0 International, as described at https://creativecommons.org/licenses/by/4.0/).
spellingShingle Methods
Morillo, Riward Campelo
Harris, Chantal T
Kennedy, Kit
Henning, Samuel R
Kafsack, Björn FC
Genome-wide profiling of histone modifications in Plasmodium falciparum using CUT&RUN
title Genome-wide profiling of histone modifications in Plasmodium falciparum using CUT&RUN
title_full Genome-wide profiling of histone modifications in Plasmodium falciparum using CUT&RUN
title_fullStr Genome-wide profiling of histone modifications in Plasmodium falciparum using CUT&RUN
title_full_unstemmed Genome-wide profiling of histone modifications in Plasmodium falciparum using CUT&RUN
title_short Genome-wide profiling of histone modifications in Plasmodium falciparum using CUT&RUN
title_sort genome-wide profiling of histone modifications in plasmodium falciparum using cut&run
topic Methods
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9670794/
https://www.ncbi.nlm.nih.gov/pubmed/36379668
http://dx.doi.org/10.26508/lsa.202201778
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