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Sample GSM790729 Query DataSets for GSM790729
Status Public on Oct 18, 2011
Title SuUR H3K27me3 ChIP
Sample type genomic
 
Channel 1
Source name H3K27me3 ChIP DNA from third instar salivary gland from SuUR
Organism Drosophila melanogaster
Characteristics cell type: third instar salivary gland
strain: SuUR-
antibody: H3K27me3 (Abcam 6002)
Treatment protocol Salivary glands were hand dissected from committed wandering third instar larvae directly into EBR medium with protease inhibitors on ice. After no more than 30 minutes samples were fixed and processed as described below.
Growth protocol Drosophila were grown on standard cornmeal, molasses agar media.
Extracted molecule genomic DNA
Extraction protocol Salivary glands were fixed with 2% formaldehyde in EBR medium for 15 min at room temperature followed by quenching with 0.125 M glycine for 5 min. The cells were washed twice with TBS and flash frozen in liquid nitrogen. Approximately 200 salivary glands were thawed, pooled, and placed in 0.5 mL of ChIP lysis buffer (50 mM HEPES/KOH pH 7.5, 140 mM NaCl, 1 mM EDTA, 1% Triton X-100, 0.1% Na-Deoxycholate). The crosslinked chromatin was sheared to an average size of 300-1000 bp by three 12-second pulses using a Branson 250 sonicator. The lysate was then centrifuged to remove cell debris. 50 uL was saved for the input DNA from each sample. The chromatin supernatant was then incubated overnight with 2 uL of antibody at 4C. After incubation with 30 uL protein G Dynabeads beads (Invitrogen) for 2h at 4C, the immune complexes were collected using the Dynal magnetic strip and washed with the following buffers at room temperature for 5 minutes each: 2X ChIP lysis buffer, 2X high salt (500mM NaCl) ChIP lysis buffer, 1X ChIP lysis buffer, 1X TE. The protein-DNA complexes were eluted from the beads in 100 uL ChIP elution buffer (50 mM Tris/HCl pH 8.0, 10 mM EDTA/1% SDS) at 65C for 15 min followed by another wash with 150 uL TE/0.67% SDS. Eluates were pooled and incubated at 65C for at least 6 hours. Input DNAs were similarly subject to reversal of crosslinks with 200 µL TE/1% SDS. Samples were treated with 100 ug proteinase K at 37C for 2 hours. DNA samples were phenol chloroform extracted twice and ethanol precipitated.
Label Cy5
Label protocol DNA was labeled using Invitrogen's BioPrime Total for Agilent aCGH labeling kit
 
Channel 2
Source name Input DNA from SuUR salivary glands
Organism Drosophila melanogaster
Characteristics cell type: third instar salivary gland
strain: SuUR-
antibody: n/a
Treatment protocol Salivary glands were hand dissected from committed wandering third instar larvae directly into EBR medium with protease inhibitors on ice. After no more than 30 minutes samples were fixed and processed as described below.
Growth protocol Drosophila were grown on standard cornmeal, molasses agar media.
Extracted molecule genomic DNA
Extraction protocol Salivary glands were fixed with 2% formaldehyde in EBR medium for 15 min at room temperature followed by quenching with 0.125 M glycine for 5 min. The cells were washed twice with TBS and flash frozen in liquid nitrogen. Approximately 200 salivary glands were thawed, pooled, and placed in 0.5 mL of ChIP lysis buffer (50 mM HEPES/KOH pH 7.5, 140 mM NaCl, 1 mM EDTA, 1% Triton X-100, 0.1% Na-Deoxycholate). The crosslinked chromatin was sheared to an average size of 300-1000 bp by three 12-second pulses using a Branson 250 sonicator. The lysate was then centrifuged to remove cell debris. 50 uL was saved for the input DNA from each sample. The chromatin supernatant was then incubated overnight with 2 uL of antibody at 4C. After incubation with 30 uL protein G Dynabeads beads (Invitrogen) for 2h at 4C, the immune complexes were collected using the Dynal magnetic strip and washed with the following buffers at room temperature for 5 minutes each: 2X ChIP lysis buffer, 2X high salt (500mM NaCl) ChIP lysis buffer, 1X ChIP lysis buffer, 1X TE. The protein-DNA complexes were eluted from the beads in 100 uL ChIP elution buffer (50 mM Tris/HCl pH 8.0, 10 mM EDTA/1% SDS) at 65C for 15 min followed by another wash with 150 uL TE/0.67% SDS. Eluates were pooled and incubated at 65C for at least 6 hours. Input DNAs were similarly subject to reversal of crosslinks with 200 µL TE/1% SDS. Samples were treated with 100 ug proteinase K at 37C for 2 hours. DNA samples were phenol chloroform extracted twice and ethanol precipitated.
Label Cy3
Label protocol DNA was labeled using Invitrogen's BioPrime Total for Agilent aCGH labeling kit
 
 
Hybridization protocol Slides were hybridized to custom Agilent tiling arrays and washed as per Agilent recommendations
Scan protocol Arrays were scanned on an Agilent scanner per manufacturer's protocol
Data processing Raw data was median normalized using the Ringo package in R in order to generate .wig files containing smoothed log ratios.
 
Submission date Sep 06, 2011
Last update date Oct 18, 2011
Contact name Terry L. Orr-Weaver
E-mail(s) weaver@wi.mit.edu
Phone 617-258-5251
Organization name Whitehead Institute for Biomedical Research
Lab Orr-Weaver
Street address 9 Cambridge Center
City Cambridge
State/province MA
ZIP/Postal code 02142
Country USA
 
Platform ID GPL11290
Series (2)
GSE31897 ChIP with anti-H3K27me3 to compare binding in salivary glands of WT and SuUR Drosophila
GSE31900 Developmental Control of Gene Copy Number by Repression of Replication Initiation and Fork Progression

Supplementary file Size Download File type/resource
GSM790729_20100519_H3K27_inp_SuUR_252532110013_051910_S01_CGH-v4_10_Apr08_1_1.wig.gz 2.1 Mb (ftp)(http) WIG
GSM790729_252532110013_051910_S01_CGH-v4_10_Apr08_1_1.txt.gz 114.5 Mb (ftp)(http) TXT
Processed data provided as supplementary file

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