|
Status |
Public on Dec 04, 2015 |
Title |
ChIP-Seq for Yrr1 protein on Saccharomyces cerevisiae cells carrying different YRR1 alleles in response to 4-nitroquinoline-N-oxide (4NQO) |
Organism |
Saccharomyces cerevisiae |
Experiment type |
Genome binding/occupancy profiling by high throughput sequencing
|
Summary |
In this study, we constructed three isogenic strains of S96 yrr1Δ background (its native YRR1 gene was knocked out) carrying three different YRR1 alleles, YRR1_S96, YRR1_YJM789, YRR1_S96-I775E, respectively. We then conducted chromatin immuno-precipitation followed by high-throughput sequencing (ChIP-Seq) for Yrr1 protein on the three strains grown in Yeast Peptone Dextrose medium (YPD) and YPD + 4NQO.
|
|
|
Overall design |
ChIP-Seq for Yrr1 protein was performed in biological triplicates on S96 cells carrying three different YRR1 alleles grown in YPD and YPD + 4NQO. Immune-precipitated DNA were sequenced for all the three cultures and input genomic DNA was sequenced for one culture.
|
|
|
Contributor(s) |
Gallagher JE, Rong-Mullins X, Dunn BL, Jiang L, Snyder MP |
Citation(s) |
24532717, 29208650 |
|
Submission date |
Nov 05, 2015 |
Last update date |
Feb 13, 2020 |
Contact name |
Xiaoqing Rong-Mullins |
Organization name |
West Virginia University
|
Street address |
53 Campus Dr
|
City |
Morgantown |
State/province |
West Virginia |
ZIP/Postal code |
26505 |
Country |
USA |
|
|
Platforms (1) |
GPL13821 |
Illumina HiSeq 2000 (Saccharomyces cerevisiae) |
|
Samples (24)
|
|
Relations |
BioProject |
PRJNA301204 |
SRA |
SRP065829 |