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Sample GSM3427003 Query DataSets for GSM3427003
Status Public on Nov 27, 2018
Title mRNA WT primed + triggered rep 1
Sample type SRA
 
Source name 3 week old Col-0 leaf tissue
Organism Arabidopsis thaliana
Characteristics tissue: true leaves 4 - 9
ecotype: Col-0
Treatment protocol For excess-light treatments, exposure to approximately 10X growth irradiance (1000 μ mol photons m-2 s-1) was applied using a mixture of 250W metal halide lamps (Venture Lighting, MH 250W/U) and high pressure sodium lamps (Phillips, SON-T 250W E E40 SL/12) providing a source of ‘warm’ light (similar to sunlight). This was applied for one hour repeated thrice daily at 9:30 am, 1:30pm, and 5:30 pm.
Growth protocol Plants grown on soil, with approximately 3g/L osmocote fertilizer, under a 12-hour photoperiod of 100-150μ mol photons m-2 s -1, 20 (±0.5) °C, and 55 (±5) % RH.
Extracted molecule polyA RNA
Extraction protocol Bisulfite-seq: Genomic DNA was extracted using the Qiagen DNeasy Plant Mini Kit (Limburg, Netherlands), as per the manufacturer’s instructions. 100-200 ng of fragmented (Covaris) and purified gDNA was bisulfite converted using the Zymo DNA-Gold bisulfite conversion kit (Zymo Research; CA, USA).
mRNA-seq: Total RNA was extracted using TRIzol reagent.
Whole genome bisulfite sequencing libraries were constructing using the Accel-NGS Methyl-Seq DNA Library Kit (Swift Biosciences; MI, USA) as per the manufacturer’s instructions.
PolyA-enriched RNA-sequencing libraries were prepared using the Illumina TruSeq Stranded mRNA Sample Preparation Kit (Illumina, CA, USA) using 1.3 μg input of extracted total RNA. The following modifications to the manufacturer’s instructions were made: reagent volumes were adjusted for 1/3 reactions; and Invitrogen SuperScript III Reverse Transcriptase (Invitrogen, Life Technologies Australia Pty Ltd) was used for first strand synthesis with adjusted reaction temperature of 50 °C.
 
Library strategy RNA-Seq
Library source transcriptomic
Library selection cDNA
Instrument model Illumina NextSeq 500
 
Data processing Bisulfite-seq
Raw reads were quality controlled using FastQC (v0.11.2), Cutadapt (v1.9), Trim Galore! (v.0.3.7).
Single-end alignments of trimmed raw reads were aligned to the TAIR10 reference using Bismark (v0.14.5) and Bowtie2 (v2.2.9) with the flags -N 0 and -L 20.
Per cytosine methylation levels were calculated using Bismark methylation extractor with default settings. Bisulfite conversion efficiency was calculated as the proportion of methylated cytosines in the CHH context within the chloroplast genome, which itself should be fully unmethylated.
Weighted methylation levels were used to calculate the proportion of CG, CHG, and CHH at single cytosine resolution to account for sequencing depth. This output was utilized in DMR identification using DSS.
mRNA-seq
Raw reads were diagnosed using FastQC (v0.11.2). Due to strong nucleotide sequence content bias Trim Galore! and Cutadapt were used to trim low-quality reads with PHRED score < 20 (-q 20) and to make a hard clip of 10 bp and 1 bp from the 5’ and 3’ ends, respectively.
Single-end alignments of trimmed raw reads were aligned to the TAIR10 reference genome using Subread (v1.6.2) with the flags -t 0 and -u to report uniquely mapping reads, prior to sorting, indexing and compressing using Samtools (v1.2).
Transcript quantification was performed at the gene-level with the Araport11 annotation using featureCounts (with flag -s 2 for reverse strand specificity). This output was utilized in differential gene expression testing with edgeR.
Genome_build: TAIR10
Supplementary_files_format_and_content: .bed.gz: weighted methylation levels at single cytosines. Separate files have been produced for each sequence of DNA methylation: CG, CHG, and CHH; . counts: counts per gene-level feature across the Araport11 annotation for each sample.
Supplementary_files_format_and_content: bed: chromosome, start, end, proportion methylated, counts methylated, counts un-methylated, total counts
 
Submission date Oct 11, 2018
Last update date Nov 29, 2018
Contact name Diep R Ganguly
E-mail(s) dganguly@sas.upenn.edu
Phone +1 215-898-0808
Organization name University of Pennsylvania
Department Department of Biology
Lab Brian Gregory
Street address 433 S University Ave
City Philadelphia
State/province PA
ZIP/Postal code 19103
Country USA
 
Platform ID GPL19580
Series (1)
GSE121150 Excess light priming in Arabidopsis thaliana genotypes with altered DNA methylomes
Relations
BioSample SAMN10232916
SRA SRX4866877

Supplementary file Size Download File type/resource
GSM3427003_P+T-r1.sorted_genes_ara11.counts.txt.gz 495.2 Kb (ftp)(http) TXT
SRA Run SelectorHelp
Raw data are available in SRA
Processed data provided as supplementary file

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