Malki, K and Tosto, MG and Pain, O and Sluyter, F and Mineur, YS and Crusio, WE and de Boer, S and Sandnabba, KN and Kesserwani, J and Robinson, E and Schalkwyk, LC and Asherson, P (2016) Comparative mRNA analysis of behavioral and genetic mouse models of aggression. American Journal of Medical Genetics Part B-Neuropsychiatric Genetics, 171 (3). pp. 427-436. DOI https://doi.org/10.1002/ajmg.b.32424
Malki, K and Tosto, MG and Pain, O and Sluyter, F and Mineur, YS and Crusio, WE and de Boer, S and Sandnabba, KN and Kesserwani, J and Robinson, E and Schalkwyk, LC and Asherson, P (2016) Comparative mRNA analysis of behavioral and genetic mouse models of aggression. American Journal of Medical Genetics Part B-Neuropsychiatric Genetics, 171 (3). pp. 427-436. DOI https://doi.org/10.1002/ajmg.b.32424
Malki, K and Tosto, MG and Pain, O and Sluyter, F and Mineur, YS and Crusio, WE and de Boer, S and Sandnabba, KN and Kesserwani, J and Robinson, E and Schalkwyk, LC and Asherson, P (2016) Comparative mRNA analysis of behavioral and genetic mouse models of aggression. American Journal of Medical Genetics Part B-Neuropsychiatric Genetics, 171 (3). pp. 427-436. DOI https://doi.org/10.1002/ajmg.b.32424
Abstract
Mouse models of aggression have traditionally compared strains, most notably BALB/cJ and C57BL/6. However, these strains were not designed to study aggression despite differences in aggression-related traits and distinct reactivity to stress. This study evaluated expression of genes differentially regulated in a stress (behavioral) mouse model of aggression with those from a recent genetic mouse model aggression. The study used a discovery-replication design using two independent mRNA studies from mouse brain tissue. The discovery study identified strain (BALB/cJ and C57BL/6J) � stress (chronic mild stress or control) interactions. Probe sets differentially regulated in the discovery set were intersected with those uncovered in the replication study, which evaluated differences between high and low aggressive animals from three strains specifically bred to study aggression. Network analysis was conducted on overlapping genes uncovered across both studies. A significant overlap was found with the genetic mouse study sharing 1,916 probe sets with the stress model. Fifty-one probe sets were found to be strongly dysregulated across both studies mapping to 50 known genes. Network analysis revealed two plausible pathways including one centered on the UBC gene hub which encodes ubiquitin, a protein well-known for protein degradation, and another on P38 MAPK. Findings from this study support the stress model of aggression, which showed remarkable molecular overlap with a genetic model. The study uncovered a set of candidate genes including the Erg2 gene, which has previously been implicated in different psychopathologies. The gene networks uncovered points at a Redox pathway as potentially being implicated in aggressive related behaviors.
Item Type: | Article |
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Uncontrolled Keywords: | aggression; mouse; BALB/c; transcriptomics |
Subjects: | Q Science > QH Natural history > QH426 Genetics |
Divisions: | Faculty of Science and Health Faculty of Science and Health > Life Sciences, School of |
SWORD Depositor: | Unnamed user with email elements@essex.ac.uk |
Depositing User: | Unnamed user with email elements@essex.ac.uk |
Date Deposited: | 22 Feb 2016 12:57 |
Last Modified: | 30 Oct 2024 16:09 |
URI: | http://repository.essex.ac.uk/id/eprint/16106 |