|
Status |
Public on Nov 24, 2021 |
Title |
210716_Solo_sir3-bahD-EcoGII_m6A_DIP |
Sample type |
SRA |
|
|
Source name |
Saccharomyces cerevisiae
|
Organism |
Saccharomyces cerevisiae |
Characteristics |
strain: JRY13438 ip antibody: anti-m6A antibody (Synaptic Systems 202-003, lot 2-109) condition: Cycling genotype: mat-delta::KanMX, sir3-bah-delta-M.ECOGII-NatMX
|
Treatment protocol |
For ChIP-seq experiments (Samples 1 and 2), cells were fixed in 1% formaldehyde for 15 minutes at 30°C and then quenched with 300mM glycine for 10min at 30°C.
|
Growth protocol |
Yeast were cultured at 30°C in YPD except for the following: Samples 21 and 22 were grown at 25°C in YPD. Samples 23 and 24 were grown at 37°C in YPD.
|
Extracted molecule |
genomic DNA |
Extraction protocol |
Cells were lysed by mechanical disruption in a bead beater. Chromatin or DNA was fragmented using sonication. V5 immunoprecipitations were performed using anti-V5 antibody (Invitrogen R960-25). m6A immunoprecipitations were performed using anti-m6A antibody (Synaptic Systems 202-003). For ChIP-seq, DNA was purified with 1X v/v SPRI Select beads (Beckman-Coulter Beckman Coulter, B23317) For ChIP-seq: NEB Ultra II library prep kit. For MeDIP-seq: Swift Biosciences Accel-NGS 1S Plus ChIP-seq and MeDIP-seq
|
|
|
Library strategy |
MeDIP-Seq |
Library source |
genomic |
Library selection |
5-methylcytidine antibody |
Instrument model |
Illumina MiniSeq |
|
|
Data processing |
FASTQ generation with Illumina Casava v2.2 Raw reads were mapped to SacCer3 genome modified to include mat∆ using Bowtie2 with following options: --local --soft-clipped-unmapped-tlen --no-unal --no-mixed --no-discordant bedgraph files were normalized to the genome-wide median (median excluded subtelomeres, chromosome III, and rDNA) Genome_build: SacCer3 (modified) Supplementary_files_format_and_content: bedGraph (normalized to genome-wide median)
|
|
|
Submission date |
Nov 17, 2021 |
Last update date |
Nov 24, 2021 |
Contact name |
Molly Brothers |
E-mail(s) |
[email protected]
|
Organization name |
University of California, Berkeley
|
Department |
Molecular and Cell Biology
|
Lab |
Rine Lab (440 Barker Hall)
|
Street address |
UC Berkeley 440 Barker Hall
|
City |
Berkeley |
State/province |
CA |
ZIP/Postal code |
94720 |
Country |
USA |
|
|
Platform ID |
GPL22715 |
Series (2) |
GSE189038 |
Distinguishing between recruitment and spread of silent chromatin structures in Saccharomyces cerevisiae [I] |
GSE190137 |
Distinguishing between recruitment and spread of silent chromatin structures in Saccharomyces cerevisiae |
|
Relations |
BioSample |
SAMN23243314 |
SRA |
SRX13158388 |