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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...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Life Science Alliance LLC
2022
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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. |
format | Online Article Text |
id | pubmed-9670794 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Life Science Alliance LLC |
record_format | MEDLINE/PubMed |
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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