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Sample GSM7912008 Query DataSets for GSM7912008
Status Public on Nov 27, 2023
Title Y1FIPuntreatedn2
Sample type SRA
 
Source name h? rpb1-Y1F::natMX6; rpb3-HA:kanMX6
Organism Schizosaccharomyces pombe
Characteristics cell line: Y1F
genotype: h? rpb1-Y1F::natMX6; rpb3-HA:kanMX6
chip antibody: HA (Millipore Sigma Roche ROAHA
treatment: none
Treatment protocol HU was added to one of the cultures to a final concentration of 12 mM, and incubation was continued for 4 hours.
Growth protocol S. pombe strains expressing rpb3-HA were grown to OD600 of 0.2 in 100 mL YES at 30oC and then split into two 50 mL cultures.
Extracted molecule genomic DNA
Extraction protocol 1.5x10^7 cells from each sample were then crosslinked with 1% formaldehyde. Extracts were prepared by bead beating and were sonicated in a Bioruptor (Diagenode; UCD-200).
ChIP-seq libraries were prepared with 2 ng of input or IP DNA using the NEBNext Ultra II DNA Library kit for Illumina (New England Biolabs).
 
Library strategy ChIP-Seq
Library source genomic
Library selection ChIP
Instrument model HiSeq X Ten
 
Description 1165_IP_C_n2
1165_IPINratio_C_n2_SESscaled.bw
Data processing Quality of the reads was determined using FastQC prior to and after trimming with TrimGalore (0.6.6)(Babraham Institute Bioinformatics https://www.bioinformatics.babraham.ac.uk/).
The trimmed reads were aligned to the reference S. pombe ASM294v2 genome using bowtie2
Aligned, deduplicated bam files were sorted and indexed in samtools
The deeptools package (version 2.0) was then used to derive bigWig files corresponding to IP/input ratios for each sample, and to scale based on read depth using the SES method.
A median genic Rpb3-HA occupancy across all protein-coding genes was computed for each bigWig file; this value was set to 1 for the wild-type control and used to scale the other bigWig files using wiggletools
Assembly: ASM294v2
Supplementary files format and content: bigWig
 
Submission date Nov 21, 2023
Last update date Nov 27, 2023
Contact name Jason Tanny
E-mail(s) jason.tanny@mcgill.ca
Organization name McGill University
Department Pharmacology and Therapeutics
Street address 3655 Prom Sir William Osler room 132
City Montreal
State/province Quebec
ZIP/Postal code H3G1Y6
Country Canada
 
Platform ID GPL30067
Series (1)
GSE248360 The Rtf1/Prf1-dependent histone modification axis and Rpb1 C-terminal domain phosphorylation counteract multi-drug resistance in fission yeast [ChIP-seq]
Relations
BioSample SAMN38345451
SRA SRX22593037

Supplementary data files not provided
SRA Run SelectorHelp
Raw data are available in SRA

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