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Status |
Public on Mar 05, 2012 |
Title |
Genome-wide analysis revealed a crosstalk between p53 and the pluripotent gene networks in mouse embryonic stem cells (ChIP-Seq) |
Organism |
Mus musculus |
Experiment type |
Genome binding/occupancy profiling by high throughput sequencing
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Summary |
Study of the function of p53 in regulating gene expression in mouse embryonic stem cells. It is critical for embryonic stem cells to maintain their genomic stability. The guardian of the genome, p53, plays important roles in maintaining the genomic integrity of ES cells through regulating the differentiation of ES cells. However, the underlying mechanism of this differentiation is still unclear. We plan to use the integrative genome-wide approach, combining ChIP-seq and gene expression microarray, to explore the mechanisms.
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Overall design |
Total six samples: two inputs (untreated and treated with adriamycin) and four ChIP samples (p53_untreated, p53_adr8h, p53S18P_untreated, p53S18P_adr8h). The two inputs will serve as controls for identifying the binding sites.
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Contributor(s) |
Huang J |
Citation(s) |
22387025, 25936916 |
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Submission date |
Dec 29, 2010 |
Last update date |
May 15, 2019 |
Contact name |
Jing Huang |
E-mail(s) |
huangj3@mail.nih.gov
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Organization name |
National Cancer Institute
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Lab |
Cancer Biology and Genetics
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Street address |
37 Convent Dr. 37/3140
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City |
Bethesda |
State/province |
MD |
ZIP/Postal code |
MD 20892 |
Country |
USA |
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Platforms (1) |
GPL9250 |
Illumina Genome Analyzer II (Mus musculus) |
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Samples (6)
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This SubSeries is part of SuperSeries: |
GSE26362 |
Whole-genome study reveals distinct mechanisms used by p53 to regulate activated and repressed genes in embryonic stem cells |
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Relations |
BioProject |
PRJNA142241 |
SRA |
SRP004907 |