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Sample GSM807216 Query DataSets for GSM807216
Status Public on Feb 06, 2012
Title HSF/D.mel_PB-seq_Rep2_seqB
Sample type SRA
 
Source name HSF IP
Organism Drosophila melanogaster
Characteristics library strategy: PB-Seq
library selection: immunoprecipitation
library source: naked, sheared genomic Drosophila S2 DNA
antibody: Anti-FLAG M2
Growth protocol Prior to DNA extraction S2 were cultured as previously described (PMID: 20844575).
Extracted molecule genomic DNA
Extraction protocol We performed an in vitro binding experiment with purified HSF and naked, sheared genomic Drosophila S2 DNA (PB-seq), to derive an accurate set of potential HSF binding sites in the Drosophila genome. HSF-bound DNA was specifically eluted and detected by high throughput sequencing. Drosophila HSF was N-terminally tagged with glutathione s-transferase and a tobacco etch virus (TEV) protease cleavage site. The C-terminus of the recombinant HSF was fused to the 3xFLAG epitope. Recombinant HSF was purified from E. coli with glutathione resin as previously described (PMID: 20078429) , with the following modifications: HSF-3xFLAG elution was achieved by addition of 6xHistidine tagged TEV protease and TEV protease was cleared from the HSF preparation using a Nickel-NTA column. We incubated 600pM HSF and 2500ng genomic DNA (sonicated to 100-600bp fragment size as previously described in PMID: 20844575) in 1500μl final volume of 1xHSF binding buffer and let it come to equilibrium for an hour at room temperature. We added 20μl ANTI-FLAG M2 affinity gel for 10 minutes, washed 8 times with 1xHSF binding buffer to remove unbound DNA; 3xFLAG peptide was added to a final concentration of 200ng/μl to specifically elute HSF and HSF-bound DNA. The mock IP was done in the absence of recombinant HSF.
 
Library strategy ChIP-Seq
Library source genomic
Library selection ChIP
Instrument model Illumina HiSeq 2000
 
Data processing The PB-seq reads were aligned to the Drosophila Genome (BDGP R5/DM3) using BWA (v 0.5.8c)
 
Submission date Oct 03, 2011
Last update date May 15, 2019
Contact name Michael Joseph Guertin
E-mail(s) [email protected]
Organization name University of Connecticut
Department Center for Cell Analysis and Modeling
Lab Molecular Genomics
Street address 400 Farmington Ave
City Farmington
State/province CT
ZIP/Postal code 06030
Country USA
 
Platform ID GPL13304
Series (1)
GSE32570 Protein/DNA in vitro Binding seq (PB-seq) for Drosophila HSF and genomic Drosophila DNA
Relations
SRA SRX099635
BioSample SAMN00736143

Supplementary file Size Download File type/resource
GSM807216_invitroB_exp2.txt_uniq.sam.gz 165.5 Mb (ftp)(http) SAM
SRA Run SelectorHelp
Raw data are available in SRA
Processed data provided as supplementary file

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