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Genome-wide ChIP-seq mapping and analysis reveal butyrate-induced acetylation of H3K9 and H3K27 correlated with transcription activity in bovine cells

Overview of attention for article published in Functional & Integrative Genomics, January 2012
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Title
Genome-wide ChIP-seq mapping and analysis reveal butyrate-induced acetylation of H3K9 and H3K27 correlated with transcription activity in bovine cells
Published in
Functional & Integrative Genomics, January 2012
DOI 10.1007/s10142-012-0263-6
Pubmed ID
Authors

Joo Heon Shin, Robert W. Li, Yuan Gao, Ransom Baldwin, Cong-jun Li

Abstract

Butyrate-induced histone acetylation plays an important role in the regulation of gene expression. However, the regulation mechanisms of histone modification remain largely unclear. To comprehensively analyze histone modification induced by butyrate, we utilized chromatin immunoprecipitation (ChIP) technology combined with next-generation sequencing technology (ChIP-seq) to analyze histone modification (acetylation) induced by butyrate and to map the epigenomic landscape of normal histone H3 and acetylated histone H3K9 and H3K27 on a large scale. To determine the location of histone H3, acetyl-H3K9, and acetyl-H3K27 binding sites within the bovine genome, we analyzed the H3-, acetyl-H3K9-, and acetyl-H3K27-enriched binding regions in the proximal promoter within 5 kb upstream, or at the 5' untranslated region (UTR) from the transcriptional start site (TSS), exon, intron, and intergenic regions (defined as regions 25 kb upstream or 10 kb downstream from the TSS). Our analysis indicated that the distribution of histone H3, acetyl-H3K9, and acetyl-H3K27 correlated with transcription activity induced by butyrate. Using the GADEM algorithm, several motifs were generated for each of the ChIP-seq datasets. A de novo search for H3, acetyl-H3K9, and acetyl-H3K27 binding motifs indicated that histone modification (acetylation) at various locations changes the histone H3 binding preferences. Our results reveal that butyrate-induced acetylation in H3K9 and H3K27 changes the sequence-based binding preference of histone H3 and underlies the potential mechanisms of gene expression regulation induced by butyrate.

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Mendeley readers

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The data shown below were compiled from readership statistics for 57 Mendeley readers of this research output. Click here to see the associated Mendeley record.

Geographical breakdown

Country Count As %
United States 1 2%
China 1 2%
Unknown 55 96%

Demographic breakdown

Readers by professional status Count As %
Student > Ph. D. Student 18 32%
Researcher 15 26%
Student > Master 6 11%
Professor 6 11%
Student > Bachelor 4 7%
Other 2 4%
Unknown 6 11%
Readers by discipline Count As %
Agricultural and Biological Sciences 30 53%
Biochemistry, Genetics and Molecular Biology 8 14%
Immunology and Microbiology 3 5%
Social Sciences 2 4%
Neuroscience 2 4%
Other 6 11%
Unknown 6 11%
Attention Score in Context

Attention Score in Context

This research output has an Altmetric Attention Score of 1. This is our high-level measure of the quality and quantity of online attention that it has received. This Attention Score, as well as the ranking and number of research outputs shown below, was calculated when the research output was last mentioned on 19 January 2012.
All research outputs
#18,303,566
of 22,661,413 outputs
Outputs from Functional & Integrative Genomics
#279
of 487 outputs
Outputs of similar age
#196,146
of 245,784 outputs
Outputs of similar age from Functional & Integrative Genomics
#2
of 3 outputs
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