U.S. flag

An official website of the United States government

Format

Send to:

Choose Destination

SRX6385189: GSM3912456: Z-1: WT rep2; Glycine max; RNA-Seq
1 ILLUMINA (Illumina MiSeq) run: 25.6M spots, 7.7G bases, 2.3Gb downloads

Submitted by: NCBI (GEO)
Study: Dynamic changes in genome-wide histone methylation and gene expression of soybean roots in response to salt stress (RNA-seq dataset)
show Abstracthide 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. 8798 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. Overall design: Transcription profile of control and salt-treated soybean roots.
Sample: Z-1: WT rep2
SAMN12172107 • SRS5044707 • All experiments • All runs
Organism: Glycine max
Library:
Instrument: Illumina MiSeq
Strategy: RNA-Seq
Source: TRANSCRIPTOMIC
Selection: cDNA
Layout: PAIRED
Construction protocol: Total RNA was extracted from the root of soybeans with TRIzol reagent (Invitrogen) according to the manufacturer's instructions. Library making, RNA-seq and data analysis were performed as described previously (Xu et al., 2018).
Experiment attributes:
GEO Accession: GSM3912456
Links:
Runs: 1 run, 25.6M spots, 7.7G bases, 2.3Gb
Run# of Spots# of BasesSizePublished
SRR962234525,632,6367.7G2.3Gb2019-10-31

ID:
8458257

Supplemental Content

Search details

See more...

Recent activity

Your browsing activity is empty.

Activity recording is turned off.

Turn recording back on

See more...