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Distinct DNA Sequence Preference for Histone Occupancy in Primary and Transformed Cells

Genome-wide occupancy of several histone modifications in various cell types has been studied using chromatin immunoprecipitation (ChIP) sequencing. Histone occupancy depends on DNA sequence features like inter-strand symmetry of base composition and periodic occurrence of TT/AT. However, whether DN...

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Autores principales: Datta, Subhamoy, Patel, Manthan, Patel, Divyesh, Singh, Umashankar
Formato: Online Artículo Texto
Lenguaje:English
Publicado: SAGE Publications 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6475841/
https://www.ncbi.nlm.nih.gov/pubmed/31037026
http://dx.doi.org/10.1177/1176935119843835
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author Datta, Subhamoy
Patel, Manthan
Patel, Divyesh
Singh, Umashankar
author_facet Datta, Subhamoy
Patel, Manthan
Patel, Divyesh
Singh, Umashankar
author_sort Datta, Subhamoy
collection PubMed
description Genome-wide occupancy of several histone modifications in various cell types has been studied using chromatin immunoprecipitation (ChIP) sequencing. Histone occupancy depends on DNA sequence features like inter-strand symmetry of base composition and periodic occurrence of TT/AT. However, whether DNA sequence motifs act as an additional effector of histone occupancy is not known. We have analyzed the presence of DNA sequence motifs in publicly available ChIP-sequence datasets for different histone modifications. Our results show that DNA sequence motifs are associated with histone occupancy, some of which are different between primary and transformed cells. The motifs for primary and transformed cells showed different levels of GC-richness and proximity to transcription start sites (TSSs). The TSSs associated with transformed or primary cell-specific motifs showed different levels of TSS flank transcription in primary and transformed cells. Interestingly, TSSs with a motif-linked occupancy of H2AFZ, a component of positioned nucleosomes, showed a distinct pattern of RNA Polymerase II (POLR2A) occupancy and TSS flank transcription in primary and transformed cells. These results indicate that DNA sequence features dictate differential histone occupancy in primary and transformed cells, and the DNA sequence motifs affect transcription through regulation of histone occupancy.
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spelling pubmed-64758412019-04-29 Distinct DNA Sequence Preference for Histone Occupancy in Primary and Transformed Cells Datta, Subhamoy Patel, Manthan Patel, Divyesh Singh, Umashankar Cancer Inform Original Research Genome-wide occupancy of several histone modifications in various cell types has been studied using chromatin immunoprecipitation (ChIP) sequencing. Histone occupancy depends on DNA sequence features like inter-strand symmetry of base composition and periodic occurrence of TT/AT. However, whether DNA sequence motifs act as an additional effector of histone occupancy is not known. We have analyzed the presence of DNA sequence motifs in publicly available ChIP-sequence datasets for different histone modifications. Our results show that DNA sequence motifs are associated with histone occupancy, some of which are different between primary and transformed cells. The motifs for primary and transformed cells showed different levels of GC-richness and proximity to transcription start sites (TSSs). The TSSs associated with transformed or primary cell-specific motifs showed different levels of TSS flank transcription in primary and transformed cells. Interestingly, TSSs with a motif-linked occupancy of H2AFZ, a component of positioned nucleosomes, showed a distinct pattern of RNA Polymerase II (POLR2A) occupancy and TSS flank transcription in primary and transformed cells. These results indicate that DNA sequence features dictate differential histone occupancy in primary and transformed cells, and the DNA sequence motifs affect transcription through regulation of histone occupancy. SAGE Publications 2019-04-19 /pmc/articles/PMC6475841/ /pubmed/31037026 http://dx.doi.org/10.1177/1176935119843835 Text en © The Author(s) 2019 http://www.creativecommons.org/licenses/by-nc/4.0/ This article is distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 License (http://www.creativecommons.org/licenses/by-nc/4.0/) which permits non-commercial use, reproduction and distribution of the work without further permission provided the original work is attributed as specified on the SAGE and Open Access pages (https://us.sagepub.com/en-us/nam/open-access-at-sage).
spellingShingle Original Research
Datta, Subhamoy
Patel, Manthan
Patel, Divyesh
Singh, Umashankar
Distinct DNA Sequence Preference for Histone Occupancy in Primary and Transformed Cells
title Distinct DNA Sequence Preference for Histone Occupancy in Primary and Transformed Cells
title_full Distinct DNA Sequence Preference for Histone Occupancy in Primary and Transformed Cells
title_fullStr Distinct DNA Sequence Preference for Histone Occupancy in Primary and Transformed Cells
title_full_unstemmed Distinct DNA Sequence Preference for Histone Occupancy in Primary and Transformed Cells
title_short Distinct DNA Sequence Preference for Histone Occupancy in Primary and Transformed Cells
title_sort distinct dna sequence preference for histone occupancy in primary and transformed cells
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6475841/
https://www.ncbi.nlm.nih.gov/pubmed/31037026
http://dx.doi.org/10.1177/1176935119843835
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