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Sample GSM4262911

Query DataSets for GSM4262911

Status

Public on Jan 22, 2020

Title

SacCer.RepTiming.30min.Replicate2

Sample type

SRA

Source name

in vitro cell culture

Organism

Saccharomyces cerevisiae

Characteristics

genotype: MATa ade2-1 his3-11,15 leu2-3,112 trp1-1 ura3-1 can1-100 bar1::hisG ars608{delta}::HIS3 ars609{delta}::TRP1 ars305::TRP1 GPD-HSV-TK ADH1-hENT1 BrdU-Inc

Treatment protocol

For the synchronized replication timing experiment, yeast cells were arrested in G1 with α-factor (100 ng/ml) for 2 hours, then released into fresh media containing (amount) 0.1mM BrdU to label one DNA strand. To maintain synchronization the culture was arrested with α-factor a second time, 40 minutes post release. This second G1 arrested culture was released again into media containing 0.1mM BrdU and 50 μg/ml pronase, flow and DNA samples were collected to monitor S-phase progression.

Growth protocol

Yeast strains were grown according to standard procedures in YPD (yeast extract, peptone, and 2% dextrose) at 30ºC

Extracted molecule

genomic DNA

Extraction protocol

DNA extraction: As RerepSeq selectively fragments rereplicated DNA and enriches those sequences by size selection, it is imperative that the genomic input DNA is of high molecular weight. For yeast samples: cells were pelleted by centrifugation at 3000 rpm for 3 minutes and resuspended in SCE (1M sorbitol, 100 mM sodium citrate, 10 mM EDTA pH 8.0); fresh 0.125% (v/v) β-mercaptoethanol and 10 U/mL zymolyase was added and incubated for 30-60 minutes at 37ºC to digest cell walls; human cells or yeast spheroplasts were pelleted by centrifugation at 3000 rpm for 3 minutes and resuspended in 500uL RIPA buffer (10 mM Tris-Cl pH 8.0, 1 mM EDTA, 1% Triton X-100, 0.1% sodium deoxycholate, 0.1% SDS, 140 mM NaCl, 1 mM PMSF) with RNase A, 0.2 mg/mL and incubated at 37ºC for 1 hour. 25uL 20% SDS and 10µl of 20 mg/ml proteinase K was then added and allowed in incubate at 55ºC for 2 hours. DNA was extracted twice using Phenol:Chloroform:Isoamyl alcohol (25:24:1, v/v) and precipitated using isopropanol. DNA was resuspended and stored in nuclease free water. RerepSeq Digestion: In an 8 strip 200 µl PCR tube 1 – 5 µg (depending on the experiment) high molecular weight genomic DNA was mixed with 2.5uL 10X Hoechst 33258 (0.1mg/ml) and 2.5uL 10X NEB Buffer 4 (50 mM Potassium Acetate, 20 mM Tris-acetate , 10 mM Magnesium Acetate, 1 mM DTT pH 7.9@25°C) to a final volume of 24uL; open tubes placed upright in PCR tube rack, covered with glass plate (3" x 3" glass plate from VWR Vertical Gel Electrophoresis Systems), exposed to 7.5 minutes of glass plate filtered (UVA only) from a Stratalinker. Following UVA treatment, samples were digested with 0.5uL UDG (5 units of Uracil-DNA Glycosylase), 0.5uL APE1 (10 units of human apurinic/apyrimidinic endonuclease 1) for 2 hours at 37C. Digested DNA was repaired with NEB’s FFPE DNA Repair Mix for 30 minutes then separated on 0.8% agarose gel for 15 minutes. Fragmented DNA ranging from 0.1Kb to 3Kb was gel extracted with Wizard® SV Gel and PCR Clean-Up System (Promega) and the purified DNA was resuspended in 50uL of water for subsequent qPCR and sequencing analysis.
Illumina Nextera DNA Flex Library Prep Kit

Library strategy

OTHER

Library source

genomic

Library selection

other

Instrument model

Illumina HiSeq 4000

Description

Yeast replication samples
SacCer.RepTiming.30min.merged.bedgraph

Data processing

Yeast fastq files were aligned to SacCer3 using bowtie2
The resulting sam files were turned into bams and duplicate reads were removed using samtools
Bam files were turned into bedgraphs using the bedtools2.29.2
If samples were sequenced for additional depth, the bam files were merged at this point (see SacCer.RepTiming data, replicates 1a and 1b)
Bedgraphs were read count normalized using an RPM calculation
RPM normalized bedgraphs were then scaled to mitochondria read percentages
The fully normalized bedgraphs were binned to 100bp and smoothed using a 10kb sliding window
To make the final processed files, replicates were merged and averaged to make a single bedgraph
Genome_build: SacCer3
Supplementary_files_format_and_content: Bedgraph normalized by RPM and mitochondria content, merged across replicates
Library strategy: Rerep-seq

Submission date

Jan 13, 2020

Last update date

Jan 22, 2020

Contact name

Joshua C Black

E-mail(s)

blacklabucd@gmail.com

Organization name

University of Colorado

Department

Pharmacology