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Status |
Public on Aug 28, 2012 |
Title |
Sirt1, p53 and p38MAPK are crucial regulators of detrimental phenotypes of ESCs with Max expression ablation |
Organism |
Mus musculus |
Experiment type |
Expression profiling by array
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Summary |
Ablation of expression of the Max gene encoding a Myc protein partner in ES cells provoked two major phenomena, i.e. loss of pluripotency and apoptotic cell death. We found that nicotinamide (Nam) significantly alleviates these Max expression ablation-coupled phenotypes in ES cells. To see the alleviation effect of Nam on the overall expression profile of Max-null ES cells whose Max expression is controlled by the tet-off system, we eliminated Max expression by adding doxycycline (Dox) in the presence of Nam.
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Overall design |
DNA microarray analyses were performed using total RNAs from Nam (4 mM)-treated Max-null ES cells that were cultured in the presence or absence of doxycycline for 6 days.
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Contributor(s) |
Hishida T, Nakachi Y, Mizuno Y, Okazaki Y, Okuda A |
Citation(s) |
22696478 |
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Submission date |
May 10, 2012 |
Last update date |
Feb 11, 2019 |
Contact name |
Akihiko Okuda |
E-mail(s) |
akiokuda@saitama-med.ac.jp
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Phone |
81-42-984-4787
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Organization name |
Saitama Medical University
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Department |
Research Center for Genomic Medicine
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Lab |
Division of Biomedical Sciences
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Street address |
1397-1 Yamane
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City |
Hidaka |
State/province |
Saitama |
ZIP/Postal code |
3501241 |
Country |
Japan |
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Platforms (1) |
GPL1261 |
[Mouse430_2] Affymetrix Mouse Genome 430 2.0 Array |
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Samples (4)
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Relations |
BioProject |
PRJNA165155 |