Abstract

Soybean is an important economic crop for human diet, animal feeds and biodiesel due to high protein and oil content. Its productivity is significantly hampered by salt stress, which impairs plant growth and development by affecting gene expression, in part, through epigenetic modification of chromatin status. However, little is known about epigenetic regulation of stress response in soybean roots. Here, we used RNA-seq and ChIP-seq technologies to study the dynamics of genome-wide transcription and histone methylation patterns in soybean roots under salt stress. Eight thousand seven hundred ninety eight soybean genes changed their expression under salt stress treatment. Whole-genome ChIP-seq study of an epigenetic repressive mark, histone H3 lysine 27 trimethylation (H3K27me3), revealed the changes in H3K27me3 deposition during the response to salt stress. Unexpectedly, we found that most of the inactivation of genes under salt stress is strongly correlated with the de novo establishment of H3K27me3 in various parts of the promoter or coding regions where there is no H3K27me3 in control plants. In addition, the soybean histone modifiers were identified which may contribute to de novo histone methylation and gene silencing under salt stress. Thus, dynamic chromatin regulation, switch between active and inactive modes, occur at target loci in order to respond to salt stress in soybean. Our analysis demonstrates histone methylation modifications are correlated with the activation or inactivation of salt-inducible genes in soybean roots.

Highlights

  • Environmental changes affect the organisms in a wide range of situations (Lopez-Maury et al, 2008)

  • We provide a comprehensive overview of the histone modifiers which may work together to regulate differential H3K27me3 modification leading to activation or inactivation of gene expression during salt stress in soybean

  • We selected to grow roots in 100 mM salt to study the impact of salt stress on gene expression in soybean (Figure 1A)

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Summary

Introduction

Environmental changes affect the organisms in a wide range of situations (Lopez-Maury et al, 2008). Specific amino acids within the N-terminal regions of histones are targets for a number of covalent modifications, including methylation, phosphorylation, ubiquitination and acetylation. Some of these marks, for example, acetylation of lysine 14 of histone H3 (H3K14ac) or trimethylation of lysine 4 of Histone (H3K4me3), are generally associated with open, actively transcribed genomic regions, whereas others, such as H3K9me or H3K27me, are indicative of a repressed chromatin state (Zhang et al, 2007; Li et al, 2008; Charron et al, 2009; Zhang et al, 2009; He et al, 2011)

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