Methylation profiling

Dataset Information

0

The major urinary protein gene cluster knockout mouse as a novel model for translational metabolism research [RRBS]


ABSTRACT: Scientific evidence suggests that not only murine scent communication is regulated by major urinary proteins, but that their expression may also vary in response to metabolism via a yet unknown mechanism. Major urinary proteins are expressed mainly in the liver, showing a sexually dimorphic pattern with substantially higher expression in males. Here, we investigate the metabolic implications of a major urinary protein knockout in twelve-week-old male and female C57BL/6N mice during ad libitum feeding. Despite both sexes of major urinary protein knockout mice displayed numerically increased body weight and visceral adipose tissue proportions compared to sex-matched wildtype mice, the main genotype-specific metabolic differences were observed exclusively in males. Male major urinary protein knockout mice exhibited plasma and hepatic lipid accumulation accompanied by a hepatic transcriptome indicating an activation of lipogenesis. These findings match the higher major urinary protein expression in male compared to female wildtype mice, suggesting a more distinct reduction in energy requirements in male compared to female major urinary protein knockout mice. The observed sex-specific anabolic phenotype confirms a role of major urinary protein in metabolism and, since major urinary proteins are not expressed in humans, suggests the major urinary protein knockout mouse as a potential alternative model for translational metabolism research which needs to be further elucidated.

ORGANISM(S): Mus musculus

PROVIDER: GSE188157 | GEO | 2022/08/01

REPOSITORIES: GEO

Similar Datasets

2022-08-01 | GSE188156 | GEO
2009-03-07 | E-GEOD-12000 | biostudies-arrayexpress
2003-12-16 | GSE864 | GEO
2010-01-19 | E-GEOD-18224 | biostudies-arrayexpress
2019-04-01 | GSE120761 | GEO
2022-10-27 | GSE216147 | GEO
2024-02-08 | GSE191112 | GEO
2024-03-05 | GSE242445 | GEO
2019-12-31 | GSE137449 | GEO
2024-05-05 | GSE266131 | GEO