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GEO help: Mouse over screen elements for information. |
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| Status |
Public on Oct 08, 2010 |
| Title |
Differential expression of genes in liver of mice with a nonfunctional helicase domain of the Wrn protein treated with resveratrol compared to untreated wild type mice. |
| Organism |
Mus musculus |
| Experiment type |
Expression profiling by array
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| Summary |
Werner syndrome (WS) is a rare disorder characterized by the premature onset of a number of age-related diseases. The gene responsible for WS is believed to be involved in different aspects of transcription, replication, and/or DNA repair. We generated a mouse model with a deletion in the helicase domain of the murine WRN homologue that recapitulates most of the WS phenotypes including an abnormal hyaluronic acid excretion, higher reactive oxygen species (ROS) levels, increased genomic instability and cancer incidence resulting in a 10-15% decreased life span expectancy. In addition, WS patients and Wrn mutant mice show hallmarks of a metabolic syndrome including premature visceral obesity, hypertriglyceridemia, insulin-resistant diabetes type 2 and associated cardiovascular diseases. In this study, we compared the expression profile of liver tissues from 9 months old Wrn mutant treated with a standard diet supplemented with 0.04% resveratrol and wild type animals fed with standard diet only. Resveratrol is a calorie restriction mimetic. Gene set enrichment analysis of the microarray data indicated that reseveratrol-treated Wrn mutant mice exhibited down-regulation of genes normally decreased in several transgenic mouse models of hepatoma. In addition, resvratrol-treated Wrn mutant mice also exhibited a decrease in the expression of genes involved fatty acid metabolism and PPAR signaling pathways. Resvratrol-treated Wrn mutant mice also increased the expression of genes involved in steroid and cholesterol biosynthesis, xenobiotic metabolisms as well as inflammation. Finally, resveratrol improved insulin-resistance and the hyperglycemia but had no impact on dyslipidemia and mean life span of Wrn mutant mice.
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| Overall design |
Microarray analyses were performed on the liver tissues of 9 months old mice. Four independent biological replicates of this experiment (wild type vs resveratrol treated Wrn helicase mutant mice) were carried out with a dye swap on two replicates of each genotype.
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| Contributor(s) |
Labbé A, Garand C, Paquet ER, Cogger VC, Le Couteur DG, Lebel M |
| Citation(s) |
20974729 |
| Submission date |
Apr 21, 2010 |
| Last update date |
May 10, 2018 |
| Contact name |
Eric R Paquet |
| Organization name |
EPFL
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| Department |
Life sciences
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| Lab |
Naef lab
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| Street address |
Station 15 CH - 1015
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| City |
Lausanne |
| State/province |
Vaud |
| ZIP/Postal code |
1015 |
| Country |
Switzerland |
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| Platforms (1) |
| GPL4134 |
Agilent-014868 Whole Mouse Genome Microarray 4x44K G4122F (Feature Number version) |
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| Samples (4)
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| GSM535721 |
Wrn protein treated with resveratrol compared to untreated wild type mice. #1 |
| GSM535722 |
Wrn protein treated with resveratrol compared to untreated wild type mice. #2 |
| GSM535723 |
Wrn protein treated with resveratrol compared to untreated wild type mice. #3 [dye-swap] |
| GSM535724 |
Wrn protein treated with resveratrol compared to untreated wild type mice. #4 [dye-swap] |
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| Relations |
| BioProject |
PRJNA126351 |
| Supplementary file |
Size |
Download |
File type/resource |
| GSE21431_RAW.tar |
30.7 Mb |
(http)(custom) |
TAR (of GPR) |
| Processed data included within Sample table |
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