Functional characterization of open chromatin in bidirectional promoters of rice

Sci Rep. 2016 Aug 25:6:32088. doi: 10.1038/srep32088.

Abstract

Bidirectional gene pairs tend to be highly coregulated and function in similar biological processes in eukaryotic genomes. Structural features and functional consequences of bidirectional promoters (BDPs) have received considerable attention among diverse species. However, the underlying mechanisms responsible for the bidirectional transcription and coexpression of BDPs remain poorly understood in plants. In this study, we integrated DNase-seq, RNA-seq, ChIP-seq and MNase-seq data and investigated the effect of physical DNase I hypersensitive site (DHS) positions on the transcription of rice BDPs. We found that the physical position of a DHS relative to the TSS of bidirectional gene pairs can affect the expression of the corresponding genes: the closer a DHS is to the TSS, the higher is the expression level of the genes. Most importantly, we observed that the distribution of DHSs plays a significant role in the regulation of transcription and the coexpression of gene pairs, which are possibly mediated by orchestrating the positioning of histone marks and canonical nucleosomes around BDPs. Our results demonstrate that the combined actions of chromatin structures with DHSs, which contain functional cis-elements for interaction with transcriptional machinery, may play an important role in the regulation of the bidirectional transcription or coexpression in rice BDPs. Our findings may help to enhance the understanding of DHSs in the regulation of bidirectional gene pairs.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Chromatin / chemistry
  • Chromatin / genetics*
  • Chromatin / metabolism
  • Chromatin Immunoprecipitation
  • Deoxyribonuclease I / metabolism
  • Gene Expression Regulation, Plant*
  • Histones / genetics
  • Histones / metabolism
  • Nucleosomes / genetics
  • Nucleosomes / metabolism
  • Oryza / genetics*
  • Promoter Regions, Genetic*
  • Sequence Analysis, RNA
  • Transcription Initiation Site

Substances

  • Chromatin
  • Histones
  • Nucleosomes
  • Deoxyribonuclease I