Abstract

BackgroundSeveral post-translational histone modifications are mainly found in gene promoters and are associated with the promoter activity. It has been hypothesized that histone modifications regulate the transcription, as opposed to the traditional view with transcription factors as the key regulators. Promoters of most active genes do not only initiate transcription of the coding sequence, but also a substantial amount of transcription of the antisense strand upstream of the transcription start site (TSS). This promoter feature has generally not been considered in previous studies of histone modifications and transcription factor binding.ResultsWe annotated protein-coding genes as bi- or unidirectional depending on their mode of transcription and compared histone modifications and transcription factor occurrences between them. We found that H3K4me3, H3K9ac, and H3K27ac were significantly more enriched upstream of the TSS in bidirectional genes compared with the unidirectional ones. In contrast, the downstream histone modification signals were similar, suggesting that the upstream histone modifications might be a consequence of transcription rather than a cause. Notably, we found well-positioned CTCF and RAD21 peaks approximately 60-80 bp upstream of the TSS in the unidirectional genes. The peak heights were related to the amount of antisense transcription and we hypothesized that CTCF and cohesin act as a barrier against antisense transcription.ConclusionsOur results provide insights into the distribution of histone modifications at promoters and suggest a novel role of CTCF and cohesin as regulators of transcriptional direction.Electronic supplementary materialThe online version of this article (doi:10.1186/s12864-015-1485-5) contains supplementary material, which is available to authorized users.

Highlights

  • Several post-translational histone modifications are mainly found in gene promoters and are associated with the promoter activity

  • In unidirectional genes we found that H2A.Z showed strongest signal upstream of the transcription start site (TSS) but in bidirectional genes the signal was stronger downstream of the TSS (Additional file 3: Figure S6 A1-I1)

  • The histone modifications (HM) H3K4me3, H3K9ac, H3K27ac, and H3K4me2 were identified to be more enriched upstream of the TSS in bidirectional genes compared with unidirectional genes

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Summary

Introduction

Several post-translational histone modifications are mainly found in gene promoters and are associated with the promoter activity. Promoters of most active genes do initiate transcription of the coding sequence, and a substantial amount of transcription of the antisense strand upstream of the transcription start site (TSS) This promoter feature has generally not been considered in previous studies of histone modifications and transcription factor binding. The classical view of gene regulation is that transcription factors (TF) bind to enhancers and promoters This leads to recruitment of RNA Pol II to the promoter and initiation of transcription. Another aspect of transcription is that several histone post-translational modifications are preferentially located in the promoter region of genes and are associated with gene activity [1,2]. The presence of antisense transcription should be considered in the analysis of gene-regulatory marks

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