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SRX10149538: GSM5100041: G1812_RNAseq_G1812_heat_rep1; Triticum urartu; RNA-Seq
1 ILLUMINA (Illumina NovaSeq 6000) run: 28.4M spots, 8.5G bases, 2.4Gb downloads

Submitted by: NCBI (GEO)
Study: Evolutionary rewiring of wheat abiotic stress responsive network by lineage-specific transposable elements I
show Abstracthide Abstract
The yield of wheat is highly impacted by environmental stresses. The combinatorial regulation of sequence-specific transcription factors(TFs) defines a regulatory network that underlies plant stress responses. Here we created a comprehensive catalog of genomic binding sites of 115 TFs underlying abiotic stress responses by leveraging DAP-seq in Triticum Urartu, along with epigenomic profiles. The majority of gene distant TF binding sites(TFBS) are embedded in transposable elements(TEs), whose functional relevance was supported by a signature of purifying selection and active epigenomic features. Furthermore, ~30% non-TE TFBS share high sequence similarity with TE-embeded TFBS, potentially derived from Triticeae-specific TEs and have almost no sequence homology in non-Triticeae species. The expansion of TE-derived TFBS in wheat linked to wheat-specific stress responsive genes, suggesting that TEs are an important driving force for regulatory innovation. Altogether, TEs have significantly and continuously shaped regulatory network in wheat adaptation. Overall design: In order to delineate the major TF regulatory circuitry to abiotic stresses in Triticum Urartu, we performed DAP-seq to obtain a genome-wide binding profile of stress response TFs, ChIP-seq for three well-studied histone modifications (including H3K9ac, H3K4me3 and H3K27me3), DNase-seq, Bisulphite-seq and RNA-seq in 5 stresses.
Sample: G1812_RNAseq_G1812_heat_rep1
SAMN18026048 • SRS8301855 • All experiments • All runs
Organism: Triticum urartu
Library:
Instrument: Illumina NovaSeq 6000
Strategy: RNA-Seq
Source: TRANSCRIPTOMIC
Selection: cDNA
Layout: PAIRED
Construction protocol: 2.2 μg DNA extracted from the harvested seedlings were used to prepare ChIP-seq, DNase-seq and Bisulphite-seq. RNA was extracted using TRIzol and 2μg total RNA were used to prepare RNA-seq. Nuclei were extracted with H1B buffer(20 mM Tris-HCl, pH 8.0, 50 mM EDTA, 5 mM spermidine, 0.15 mM spermine, 40% glycerol, and 0.1% mercaptoethanol) for DNase-seq. Libraries were prepared for sequencing using standard Illumina protocols.
Experiment attributes:
GEO Accession: GSM5100041
Links:
Runs: 1 run, 28.4M spots, 8.5G bases, 2.4Gb
Run# of Spots# of BasesSizePublished
SRR1376287128,434,1768.5G2.4Gb2021-09-01

ID:
13277114

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