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Status |
Public on Mar 31, 2014 |
Title |
Rec8_4h_input |
Sample type |
genomic |
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|
Source name |
WCE at 4h after meiotic induction (REC8-HA cells)
|
Organism |
Schizosaccharomyces pombe |
Characteristics |
strain: wild type (pat1-114) culture: 4h after transfer to EMM containing nitrogen (0.05% NH4Cl) at 34ºC
|
Treatment protocol |
The cells were fixed in 1% formaldehyde for 15 min at room temperature and then incubated on ice for 45 min. The cells were washed with ice-cold PBS twice, freezed with liquid nitrogen, and stored at -80ºC.
|
Growth protocol |
For the synchronous induction of meiosis, the pat1-114 mutant strain was cultured in EMM medium containing nitrogen (0.5% NH4Cl) at 25ºC. This culture was washed and re-suspended in EMM medium without nitrogen and starved for 20 h at 25ºC to arrest the cell cycle in G1. The cells were then released into EMM containing nitrogen (0.05% NH4Cl) at 34ºC to allow for synchronous progression into meiosis.
|
Extracted molecule |
genomic DNA |
Extraction protocol |
The cells were disrupted using Multi-Beads Shocker (YASUI KIKAI, Osaka) with 0.5-mm zirconia beads. Cell lysates were sonicated to obtain average 500 bp of genomic DNA fragments. Whole cell extracts (WCEs) were subjected to immunoprecipitation with anti-HA antibody 16B12 (Covance) coupled to Dynabeads protein A (Invitrogen). A small amount of WCEs was used as input sample. The chromatin immunoprecipitated sample and input sample were incubated overnight at 75ºC, incubated for 3 hours at 55ºC with proteinase K, and DNA was purified using QIAquick Spin Purification Kit (QIAGEN).
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Label |
biotin
|
Label protocol |
Immunoprecipitated DNA and input DNA were amplified and end-labeled with the IVT (in vitro transcription). The amplification method is as described elsewhere (Katou et al., 2006).
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|
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Hybridization protocol |
16 h at 45C using a hybridization oven 640 (affymetrix) as described in the Affymetrix Chromatin Immunoprecipitation Assay Protocol (P/N 702238 Rev. 3)
|
Scan protocol |
Fluidics station 400 protocol Midi-euk2.v3 (affymetrix) was performed to wash and stain arrays. The arrays were scanned on GeneChip Scanner 3000 7G (affymetrix).
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Data processing |
Quantile normalization and calculation of MA statistics (bar file) were performed with CisGenome v2 (Ji et al., 2008).
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Submission date |
Dec 02, 2013 |
Last update date |
Mar 31, 2014 |
Contact name |
Masaru Ito |
Organization name |
Osaka University
|
Street address |
Yamadaoka 3-2
|
City |
Suita |
State/province |
Osaka |
ZIP/Postal code |
565-0871 |
Country |
Japan |
|
|
Platform ID |
GPL7715 |
Series (2) |
GSE52858 |
Meiotic recombination cold spots in chromosomal cohesion sites [ChIP-chip] |
GSE52863 |
Meiotic recombination cold spots in chromosomal cohesion sites |
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