Abstract

BackgroundTranscriptional regulation is impacted by multiple layers of genome organization. A general feature of transcriptionally active chromatin is sensitivity to DNase I and association with acetylated histones. However, very few of these active DNase I-sensitive domains, such as the chicken erythrocyte β-globin domain, have been identified and characterized. In chicken polychromatic erythrocytes, dynamically acetylated histones associated with DNase I-sensitive, transcriptionally active chromatin prevent histone H1/H5-induced insolubility at physiological ionic strength.ResultsHere, we identified and mapped out all the transcriptionally active chromosomal domains in the chicken polychromatic erythrocyte genome by combining a powerful chromatin fractionation method with next-generation DNA and RNA sequencing. Two classes of transcribed chromatin organizations were identified on the basis of the extent of solubility at physiological ionic strength. Highly transcribed genes were present in multigenic salt-soluble chromatin domains ranging in length from 30 to over 150 kb. We identified over 100 highly expressed genes that were organized in broad dynamically highly acetylated, salt-soluble chromatin domains. Highly expressed genes were associated with H3K4me3 and H3K27ac and produced discernible antisense transcripts. The moderately- and low-expressing genes had highly acetylated, salt-soluble chromatin regions confined to the 5′ end of the gene.ConclusionsOur data provide a genome-wide profile of chromatin signatures in relation to expression levels in chicken polychromatic erythrocytes.Electronic supplementary materialThe online version of this article (doi:10.1186/s13072-016-0068-2) contains supplementary material, which is available to authorized users.

Highlights

  • IntroductionA general feature of transcriptionally active chromatin is sensitivity to DNase I and association with acetylated histones

  • Transcriptional regulation is impacted by multiple layers of genome organization

  • Genome‐wide mapping of polychromatic erythrocyte transcribed chromosomal domains To isolate fraction F1 chromatin, chicken polychromatic erythrocyte nuclei were incubated with micrococcal nuclease, bulk chromatin (SE) was released, and chromatin fragments soluble at 150 mM NaCl were isolated and size-resolved [23]

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Summary

Introduction

A general feature of transcriptionally active chromatin is sensitivity to DNase I and association with acetylated histones. Dynamically acetylated histones associated with DNase I-sensitive, transcriptionally active chromatin prevent histone H1/H5-induced insolubility at physiological ionic strength. Genomic mapping of acetylated histones (H3K9/14ac, H4K16ac) demonstrated that the acetylated histones are located around the transcription start site of expressed genes [2,3,4]. For α- and β-globin genes in mammalian and chicken erythroid cells, the dynamically highly acetylated histones are broadly distributed to encompass transcriptionally competent and active globin genes.

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