| First Author | Davis KC | Year | 2020 |
| Journal | Front Neurosci | Volume | 14 |
| Pages | 139 | PubMed ID | 32153359 |
| Mgi Jnum | J:289570 | Mgi Id | MGI:6433706 |
| Doi | 10.3389/fnins.2020.00139 | Citation | Davis KC, et al. (2020) Behavioral Alterations in Mice Carrying Homozygous HDAC4 (A778T) Missense Mutation Associated With Eating Disorder. Front Neurosci 14:139 |
| abstractText | Eating disorders (EDs) are serious mental illnesses thought to arise from the complex gene-environment interactions. DNA methylation patterns in histone deacetylase 4 (HDAC4) locus have been associated with EDs and we have previously identified a missense mutation in the HDAC4 gene (HDAC4 (A786T) ) that increases the risk of developing an ED. In order to evaluate the biological consequences of this variant and establish a useful mouse model of EDs, here we performed behavioral characterization of mice homozygous for Hdac4 (A778T) (corresponding to human HDAC4 (A786T) ) that were further backcrossed onto C57BL/6 background. When fed high-fat diet, male, but not female, homozygous mice showed a trend toward decreased weight gain compared to their wild-type littermates. Behaviorally, male, but not female, homozygous mice spent less time in eating and exhibited reduced motivation to work for palatable food and light phase-specific decrease in locomotor activity. Additionally, homozygous Hdac4 (A778T) female, but not male, mice display social subordination when subjected to a tube dominance test. Collectively, these results reveal a complex sex- and circadian-dependent role of ED-associated Hdac4 (A778T) mutation in affecting mouse behaviors. Homozygous Hdac4 (A778T) mice could therefore be a useful animal model to gain insight into the neurobiological basis of EDs. |
