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Sample GSM2563717 Query DataSets for GSM2563717
Status Public on Oct 29, 2017
Title 0 mg/ml curcumin treatment _4h : replicate 1
Sample type SRA
 
Source name 0 ug/ml curcumin treatment 4h
Organism Dictyostelium discoideum
Characteristics strain: AX4
genotype: WT
replicate: 1
treatment concentreation: 0 mg/ml
different durations: 4 hr
Treatment protocol Cells were treated with curcumin at multiple concentrations (0, 2.5, 5.0, 7.5 and 10.0 µg/ml) and samples at different time points (0, 4, 8 and 12 hour).
Growth protocol Wild-type strain (AX4) were cultured axenically in HL5.
Extracted molecule total RNA
Extraction protocol At each time point, we harvested the cells directly into 1 mL of Trizol® (life technologies, CA, USA) and extracted total RNA according to the manufacturer’s recommended protocol. We performed two rounds of poly-A selection and fragmented 100 ng of the resulting mRNA into approximately 200 bases fragments. We prepared cDNA and the second strand.
We prepared two sets of Illumina multiplexed libraries. We prepared 48 individual libraries separately and deveided two sets. In each set, we added a unique barcode to each library at the final step of PCR amplification. We pooled equal amounts of DNA from each library and sequenced one pool per lane of a flow cell on Illumina Genome Analyzer II (read length = 50 bases).
 
Library strategy RNA-Seq
Library source transcriptomic
Library selection cDNA
Instrument model Illumina Genome Analyzer II
 
Data processing After demultiplexing, the data was mapped to the D. discoideum genome with bowtie version 1.0.0. Read qualities were used. Other parameters: seed length = 28, allowed mismatches = 2, allowed up to 1 alignment per read, with bowtie options -a, --strata, --best. Unmapped reads were trimmed from 3' by 2 nucleotides, which was repeated 5 times.
Raw expression values were computed as the number of reads that were uniquely mapped to gene exons.
Normalized expression were scaled with mappable exon lengths. This normalization is similar to the RPKM normalization (Reads Per Kilobase of exon per Megabase of library size), but instead of dividing by exon lengths we used the uniquely mappable parts of the exon. To obtain uniquely mappable parts, all possible subsequences of the reference genome (of the same length as reads in raw data) are mapped back to the reference genome, obtaining the number of uniquely mapped sequences to the exons (Exon_mappable). As a library size we used the total number of all uniquely mapped reads from the experiment, excluding the non-polyadenylated genes (N_unique). Normalized expressions were computed as follows: Exp = 10^9*raw/(N_unique * Exon_mappable).
Genome_build: D. discoideum Chromosomal DNA: 1,2,3,4,5,6,M, and floating contigs (created: 05-13-2009 13:53) from the DictyBase (chromosomes 1,2,3,4,5,6 and mitochondrial DNA are the same as on NCBI assembly "dicty_2.7"). Regions [3016085, 3768655] from chr2, [64985, 72996] from chrBF and [42801, 78150] from chrR were masked.
Supplementary_files_format_and_content: Processed data files are tab-separated files with two columns: the first containing gene names and the second its expression. Files ending with "_rc.tab" contain raw expression values while files ending with "_nor.tab" contain normalized expression values.
 
Submission date Apr 04, 2017
Last update date May 15, 2019
Contact name Gad Shaulsky
E-mail(s) gadi@bcm.edu
Organization name Baylor College of Medicine
Department Molecular and Human Genetics
Street address One Baylor Plaza
City Houston
State/province TX
ZIP/Postal code 77030
Country USA
 
Platform ID GPL9379
Series (1)
GSE97392 Curcumin affects gene expression and reactive oxygen species via a PKA dependent mechanism in Dictyostelium discoideum
Relations
BioSample SAMN06684283
SRA SRX2705537

Supplementary file Size Download File type/resource
GSM2563717_cur_bio1_04h_0_nor.tab.gz 97.0 Kb (ftp)(http) TAB
GSM2563717_cur_bio1_04h_0_rc.tab.gz 48.7 Kb (ftp)(http) TAB
SRA Run SelectorHelp
Raw data are available in SRA
Processed data provided as supplementary file

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