|  Help  |  About  |  Contact Us

Publication : APOE<sup>episilon3/epsilon4</sup> and APOE<sup>epsilon4/epsilon4</sup> genotypes drive unique gene signatures in the cortex of young mice

First Author  Foley KE Year  2021
Journal  bioRxiv Mgi Jnum  J:300626
Mgi Id  MGI:6504008 Doi  10.1101/2020.10.28.359422
Citation  Foley KE, et al. (2021) APOEepisilon3/epsilon4 and APOEepsilon4/epsilon4 genotypes drive unique gene signatures in the cortex of young mice. bioRxiv
abstractText  Restrictions on mouse models have significantly impacted research towards understanding the most common genotype contributing to dementia in the human population – APOEe3/e4. To address this, as part of MODEL-AD, we created new versions of humanized APOEε4 and APOEe3 mice on a C57BL/6J background that allow for unrestricted distribution and breeding. Methods: To determine similarities and differences between APOEe3/e4 and APOEe4/e4 risk genotypes, we analyzed peripheral lipid concentrations as well as performed unbiased transcriptional profiling of the cortex at two and four months of age, comparing APOEe3/e4 and APOEe4/e4 to the reference APOEe3/e3. To further compare APOE genotypes, cohorts of APOEe3/e3, APOEe3/e4, and APOEe4/e4 mice were exercised by voluntary running from 1 month to 4 months of age. Results: Cholesterol composition was significantly influenced by APOE genotype as early as 2 months, while triglycerides were affected by APOE genotype at 4 months. Importantly, RNA-sequencing of the cortex followed by linear modeling or weighted gene co-expression network analysis (WGCNA) revealed that the APOEe3/e4 genotype showed unique transcriptomic signatures to that 41 of APOEe4/e4. Functional enrichment of the APOEe3/e4, but not APOEε3/ε4 genotype, revealed sulfur and heparin binding as significant terms at 2 months, and extracellular matrix and blood coagulation at 4 months. Further, cell specific contributions of significant genes identified endothelial cells as overrepresented in the APOEe3/e4 but not APOEe4/e4 genotype. WGCNA analysis confirmed findings from linear modeling but also predicted that running at a young age 46 affects myelination and gliogenesis across APOE genotypes.
Quick Links:
 
Quick Links:
 

Expression

Publication --> Expression annotations

 

Other

0 Bio Entities

0 Expression