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SRX11830978: GSM5530078: ChIP-seq with no HA tag present [C-2]; [Candida] glabrata CBS 138; ChIP-Seq
1 ILLUMINA (Illumina HiSeq 2500) run: 20.8M spots, 6.3G bases, 2.9Gb downloads

Submitted by: NCBI (GEO)
Study: ChIP-seq analysis of transcription factor Upc2A binding across the Candida glabrata genome [Upc2A ChIP-seq]
show Abstracthide Abstract
To determine the genomic binding sites for the Candida glabrata transcription factor Upc2A, we utilized three different strains. One was the wild-type KKY2001 which contains a wild-type copy of UPC2A but lacks any HA tag. The other two are both derived from KKY2001 but contain a 3X HA tag immediately after the start codon of UPC2A. These strains are BVGC82 and BVGC84, respectively. Both contain a single copy of a loxP element located 252 bp downstream from the UPC2A stop codon. BVGC82 contains a wild-type copy of the UPC2A gene while BVGC84 contains a mutant form of UPC2A (G898D) that confers elevated resistance to fluconazole. ChIP was performed with anti-HA antibodies in all cases. Strains containing the wild-type UPC2A gene (no HA tag) are referred to as C1 and C2. Strains containing the 3X HA epitope tag at the N-terminus of the wild-type UPC2A gene are referred to as wt1 and wt2. These same strains challenged with fluconazole prior to ChIP are referred to as wtf1 and wtf2. The strain containing the G898D UPC2A allele are referred to as M1 and M2 (no fluconazole challenge) and MF1 and MF2 (with fluconazole challenge. Overall design: ChIP-seq using anti-HA antibody against strains expressing HA-tagged Upc2A as a wild-type protein or a gain-of-function form (G899D Upc2A). Prior to chromatin preparation and shearing, parallel cultures were either left untreated or challenged with 20 microgram/ml of fluconazole for two hours at 30 degrees C.
Sample: ChIP-seq with no HA tag present [C-2]
SAMN20864024 • SRS9844530 • All experiments • All runs
Library:
Instrument: Illumina HiSeq 2500
Strategy: ChIP-Seq
Source: GENOMIC
Selection: ChIP
Layout: PAIRED
Construction protocol: Cells were fixed with 1% formaldehyde (Sigma-Aldrich) for 15 min at room temperature with mild shaking [120-150 rpm]. The fixing reaction was stopped with 250 mM glycine (RPI) for 15 min at room temperature with mild shaking [120-150 rpm]. Cells were centrifuged and washed once with PBS. The cell pellet was resuspended in lysis buffer [50mM Hepes pH 7.5, 140mM NaCl, 1mM EDTA, 1% Triton X-100, 0.1% Sodium deoxycholate, 1mM PMSF, 1x protease inhibitor cocktail (Roche Applied Science, Penzberg, Germany). Cells were then lysed with 1 ml glass beads (Scientific Industries Inc, Bohemia, NY) at 4oC for 10 min. Both cell lysate and debris were collected and subsequently transferred to an AFA fiber pre-slit snap-cap [6 x 15mm] microtube (Covaris, Woburn, MA) for additional cellular lysis and DNA shearing. Genomic DNA was sheared with E220 focused-ultrasonicator (Covaris) [peak incident power: 75 W, duty factor: 10%, cycles per burst: 200, treatment time: 16 min, temperature: 10oC max, sample volume: 130 µl.] The sheared sample was centrifuged and the clear lysate was collected. Upc2A was immunoprecipitated with Dyna beads-protein G magnetic beads (Invitrogen, Carlsbad, CA) and anti-HA antibody (Invitrogen) [1:50 dilution] overnight at 4oC. Beads were then washed twice with lysis buffer, once with lysis buffer+ 500mM NaCl, once with LiCl buffer [10 mM Tris pH 8, 250 mM LiCl, 0.5% P-40, 0.5% Sodiumdeoxycholate, and 1 mM EDTA], and once with Tris-EDTA buffer. Beads were resuspended in TE and treated with RNAse A (Thermo Fisher Scientific) at 37oC for 30 min. Beads were then washed once with Tris-EDTA buffer, resuspended in Tris-EDTA buffer with 1% SDS, and incubate at 65oC for at least 5 hours to reverse crosslink. Eluted DNA was subsequently purified with mini elite clean-up kit (Qiagen). Qubit fluorometric assay (Thermo Fisher Scientific) was used to analyze the yield quantity and Agilent Bioanalyzer (Agilent Technology, Santa Clara, CA) was used to determine the average sheared DNA size. All ChIPed DNA libraries were generated with Accel-NGS plus DNA library kit (Swift Biosciences, Ann Arbor, MI) according to the manufacturer's instructions.
Experiment attributes:
GEO Accession: GSM5530078
Links:
Runs: 1 run, 20.8M spots, 6.3G bases, 2.9Gb
Run# of Spots# of BasesSizePublished
SRR1553264320,792,2036.3G2.9Gb2021-09-24

ID:
15748039

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