U.S. flag

An official website of the United States government

Format

Send to:

Choose Destination

SRX9908782: GSM5028849: TM-1-leaf_rep1; Gossypium hirsutum; RNA-Seq
1 ILLUMINA (HiSeq X Ten) run: 32.3M spots, 9.7G bases, 3.2Gb downloads

Submitted by: NCBI (GEO)
Study: Profiling of H3K4me3 and H3K27me3 and their roles in regulating gene transcription in allotetraploid cotton (RNA-Seq)
show Abstracthide Abstract
Cotton is an excellent model for studying heterosis, crop domestication and bioengineering improvement. Chromatin profiling helps to reveal how histone modifications are involved in controlling differential gene expression between A and D subgenome in allotetraploid cotton. However, the detailed profiling and functional characterization of H3K27me3 and H3K4me3/H3K27me3 bivalent mark are still understudied in cotton. In this study, we conducted H3K4me3 and H3K27me3-related ChIP-seq followed by comprehensively characterizing their roles in regulating gene transcription in cotton. We found that H3K4me3 and H3K27me3 exhibited active and repressive roles in regulating expression of genes between A and D subgenome, respectively. Expression of H3K4me3-H3K27me3 bivalent genes was regulated by combinatorial actions of both marks and may be dominantly controlled by H3K4me3. More importantly, H3K4me3 exhibited enrichment levels, positioning and distance-related effects on expression levels of related genes. In addition, H3K4me3, H3K27me3 and bivalent mark can indirectly influence gene expression through TF-mediated regulatory networks. Thus, our study provides insights in functions of H3K4me3 and H3K27me3 in regulating differential gene expression between A and D subgenome in cotton. Overall design: RNA-seq,ChIP-seq
Sample: TM-1-leaf_rep1
SAMN17469061 • SRS8087018 • All experiments • All runs
Library:
Instrument: HiSeq X Ten
Strategy: RNA-Seq
Source: TRANSCRIPTOMIC
Selection: cDNA
Layout: PAIRED
Construction protocol: Total RNAs were prepared using Trizol followed by DNase I treatment and removal of majority of mRNAs with oligo(T)-conjugated magnetic beads. The enriched mRNA was subse- quently used for RNA-seq library preparation following the standard protocol for preparing Illumina RNA-seq libraries.
Experiment attributes:
GEO Accession: GSM5028849
Links:
Runs: 1 run, 32.3M spots, 9.7G bases, 3.2Gb
Run# of Spots# of BasesSizePublished
SRR1349678132,263,1069.7G3.2Gb2021-12-01

ID:
12968074

Supplemental Content

Search details

See more...

Recent activity

Your browsing activity is empty.

Activity recording is turned off.

Turn recording back on

See more...