Select conditions below to toggle them from the plot:
GROUP | CONDITION | SAMPLES |
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129S1/SvImJ |
GSM5534373 GSM5534374 GSM5534381
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GSM5534375 GSM5534376 GSM5534377 GSM5534378 GSM5534380
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A/J |
GSM5534391 GSM5534394
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GSM5534384 GSM5534385 GSM5534386 GSM5534389
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C57BL/6J |
GSM5534355
|
|
GSM5534348 GSM5534350
|
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CAST/EiJ |
GSM5534401 GSM5534407
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GSM5534396 GSM5534402 GSM5534404
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||
DBA/2J |
GSM5534364
|
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GSM5534366 GSM5534369 GSM5534370
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NOD/ShiLtJ |
GSM5534410 GSM5534413
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|
NZO/HlLtJ |
GSM5534425
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GSM5534421 GSM5534423 GSM5534427
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PWK/PhJ |
GSM5534435 GSM5534439
|
|
WSB/EiJ |
GSM5534442 GSM5534453
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|
GSM5534448
|
Submission Date: Aug 24, 2021
Summary: Overweight and obesity are increasingly common public health issues worldwide, leading to a wide range of diseases from metabolic syndrome to steatohepatitis and cardiovascular diseases. While the increase in the prevalence of obesity is partly attributable to changes in lifestyle (i.e. increased sedentarity and changes in eating behaviour), the metabolic and clinical impacts of these obesogenic conditions varies between sexes and genetic backgrounds. The conception of personalised treatments of obesity and its complications require a thorough understanding of the diversity of responses to conditions such as high-fat diet intake. By analysing nine genetically diverse mouse strains, we show that much like humans, mice respond to high-fat diet in a genetic- and sex-dependent manner. Results: Physiological and molecular responses to high-fat diet are associated with expression of genes involved in immunity and mitochondrial function. Finally, we find that mitochondrial function and supercomplex assembly may explain part of the diversity of physiological responses. By exploring the complex interactions between genetics and metabolic phenotypes via gene expression and molecular traits, we shed light on the importance of genetic background and sex in determining metabolic outcomes. In addition to providing the community with an extensive resource for optimizing future experiments, our work serves as an exemplary design for more generalizable translational studies.
GEO Accession ID: GSE182668
PMID: 35677645
Submission Date: Aug 24, 2021
Summary: Overweight and obesity are increasingly common public health issues worldwide, leading to a wide range of diseases from metabolic syndrome to steatohepatitis and cardiovascular diseases. While the increase in the prevalence of obesity is partly attributable to changes in lifestyle (i.e. increased sedentarity and changes in eating behaviour), the metabolic and clinical impacts of these obesogenic conditions varies between sexes and genetic backgrounds. The conception of personalised treatments of obesity and its complications require a thorough understanding of the diversity of responses to conditions such as high-fat diet intake. By analysing nine genetically diverse mouse strains, we show that much like humans, mice respond to high-fat diet in a genetic- and sex-dependent manner. Results: Physiological and molecular responses to high-fat diet are associated with expression of genes involved in immunity and mitochondrial function. Finally, we find that mitochondrial function and supercomplex assembly may explain part of the diversity of physiological responses. By exploring the complex interactions between genetics and metabolic phenotypes via gene expression and molecular traits, we shed light on the importance of genetic background and sex in determining metabolic outcomes. In addition to providing the community with an extensive resource for optimizing future experiments, our work serves as an exemplary design for more generalizable translational studies.
GEO Accession ID: GSE182668
PMID: 35677645
Signatures:
Control Condition
Perturbation Condition
Only conditions with at least 1 replicate are available to select
This pipeline enables you to analyze and visualize your bulk RNA sequencing datasets with an array of downstream analysis and visualization tools. The pipeline includes: PCA analysis, Clustergrammer interactive heatmap, library size analysis, differential gene expression analysis, enrichment analysis, and L1000 small molecule search.