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Sample GSM590119 Query DataSets for GSM590119
Status Public on Apr 27, 2012
Title E14-serum_H3K36me3
Sample type SRA
 
Source name Embryonic Stem cells
Organism Mus musculus
Characteristics strain: 129/Ola
cell type: ES-cells
chip antibody: H3K36me3
chip antibody vendor: Diagenode
chip antibody catalog#: CS-058-100
chip antibody batch/lot#: A114-001
Treatment protocol No specific treatments
Growth protocol Embryonic stem cells were cultured without feeders in the presence of leukaemia inhibitory factor (LIF) either in medium containing 10% foetal calf serum or in serum-free medium containing the MEK inhibitor PD0325901 (1uM) and the Gsk3 inhibitor CH99021 (3uM), together known as 2i. TNGA female ES cells on a mixed strain 129 and C57BL/6 background and female and male NOD ES cells from the non-obese diabetic strain were derived in 2i. TNGA cells are heterozygous for knock-in of eGFP to the Nanog gene. The female XT67E1 line originates from a mixed 129 and PGK/C3H background, and contains a monoallelic deletion in the Xist gene. E14Tg2a, RGD2 and HM1 cells are male ES cells of 129 background, established and grown in serum without feeders according to standard protocols.
Extracted molecule genomic DNA
Extraction protocol ChIP experiments were performed using 3.3x106 cells and 3µg antibody per ChIP according to standard protocols as described with two minor modifications. Crosslinking of the cells was performed on the culture plates for 20 minutes, while ChIPed DNA was purified by Qiaquick PCR purification Kit (Qiagen). ChIP enrichment levels were analyzed by qPCR for quality control. Total RNA was isolated using Trizol (Invitrogen) and subjected to chloroform extraction, isopropanol precipitation and ethanol washing according to the manufacturer's recommendations. 100µg total RNA was subjected to two rounds of poly(A) selection using the Oligotex mRNA Mini Kit (Qiagen), followed by DNaseI treatment (Qiagen). 100-200ng mRNA was fragmented by hydrolysis (5x fragmentation buffer: 200mM Tris acetate, pH8.2, 500mM potassium acetate and 150mM magnesium acetate) at 94°C for 90 seconds and purified using the RNAeasy Minelute Kit (Qiagen). The fragmented mRNA was used as template for cDNA synthesis using 5µg random hexamers using Superscript III Reverse Transcriptase (Invitrogen) according to the manufacturer's recommendations. Ds-cDNA was synthesized in second strand buffer (Invitrogen) according to the manufacturer's recommendations and purified using the Minelute Reaction Cleanup Kit (Qiagen). Quality control was performed by qPCR.
 
Library strategy ChIP-Seq
Library source genomic
Library selection ChIP
Instrument model Illumina Genome Analyzer IIx
 
Description Chromatin IP against H3K36me3
Data processing ChIP DNA or ds-cDNA samples were prepared for sequencing by end repair of 20 ng DNA as measured by Qubit (Invitrogen). Adaptors were ligated to DNA fragments, which were subsequently size selected (~300bp). The adapter-modified DNA fragments were subjected to limited PCR amplification (14 cycles). Quality control was made by qPCR and by running the products on a Bioanalyzer (BioRad). Finally, cluster generation and sequencing-by-synthesis (36 bp) was performed using the Illumina Genome Analyzer IIx (GAIIx) platform according to standard protocols of the manufacturer (Illumina). The image files generated by the Genome Analyzer were processed to extract DNA sequence data. Sequences were aligned to the mouse MM9 reference genome using the Illumina Analysis Pipeline allowing one mismatch. Samples were sequenced to a depth of approximately 10-20 million mapped tags per sample (Table S1). Unless specified otherwise, only the tags uniquely aligning to the genome were considered for further analysis. For RNA-Seq, further analysis was performed using the 36 bp sequence reads. For ChIP-Seq, the 36 bp sequence reads were directionally extended to 300 bp, corresponding to the length of the original fragments used for sequencing, and tags mapping on exact the same genomic locus were discarded to obtain a non-redundant set. The output data were converted to Browser Extensible Data (BED) files for downstream analysis and Wiggle (WIG) files for viewing the data in the UCSC Genome Browser. All ChIP-Seq and RNA-Seq sequence analyses were conducted based on the Mus musculus NCBI m37 genome assembly (MM9) accessed from the Ensembl (release 54; May 2009) or the UCSC (assembly July 2007) Genome Browsers.
 
Submission date Sep 02, 2010
Last update date May 15, 2019
Contact name Hendrik Marks
E-mail h.marks@ncmls.ru.nl
Organization name Radboud University Nijmegen, RIMLS
Department Molecular Biology
Street address Geert Grooteplein 26/28
City Nijmegen
ZIP/Postal code 6525GA
Country Netherlands
 
Platform ID GPL11002
Series (1)
GSE23943 Epigenome and transcriptome of naive pluripotent mouse embryonic stem (ES) cells cultured in 2i serum-free medium
Relations
SRA SRX026280
BioSample SAMN00109951
Named Annotation GSM590119_E14-serum_H3K36me3-ChIP_Seq.bed.gz
Named Annotation GSM590119_E14-serum_H3K36me3-ChIP_Seq.wig.gz

Supplementary file Size Download File type/resource
GSM590119_E14-serum_H3K36me3-ChIP_Seq.bed.gz 77.8 Mb (ftp)(http) BED
GSM590119_E14-serum_H3K36me3-ChIP_Seq.wig.gz 16.7 Mb (ftp)(http) WIG
SRA Run SelectorHelp
Processed data provided as supplementary file
Raw data are available in SRA
Processed data included within Sample table

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