Search bioRxiv⌕ Search

bioRxiv · 10.1101/493692

Detailed analysis of paternal knockout Grb10 mice suggests effects on social stability, rather than social dominance

Abstract

Imprinted genes are highly expressed in monoaminergic regions of the midbrain and their functions in this area are thought to have an impact on mammalian social behaviors. One such imprinted gene is Grb10, of which the paternal allele is currently recognized as mediating social dominance behavior. However, there has been no detailed study of social dominance in Grb10+/p mice. Moreover, the original study examined tube-test behavior in isolated mice 10 months of age. Isolation testing favors more territorial and aggressive behaviors, and does not address social dominance strategies employed in group housing contexts. Furthermore, isolation stress impacts midbrain function and dominance related behavior, often through alterations in monoaminergic signaling. Thus, we undertook a systematic study of Grb10+/p social rank and dominance behavior within the cage group, using a number of convergent behavioral tests. We examined both male and female mice to account for sex differences, and tested cohorts aged 2, 6, and 10 months to examine any developments related to age. We found group-housed Grb10+/p mice do not show evidence of enhanced social dominance, but cages containing Grb10+/p and wildtype mice lacked the normal correlation between three different measures of social rank. Moreover, a separate study indicated isolation stress induced inconsistent changes in tube test behavior. Taken together, these data suggest future research on Grb10+/p mice should focus on social stability, rather than dominance per se.

Source connections

Explore related subjects

Keep this discovery

Explore connections, maps & timelines

BibTeXRIS

Rienecker, K., Chavasse, A., Moorwood, K., Ward, A., Isles, A.. 2018-12-20. Detailed analysis of paternal knockout Grb10 mice suggests effects on social stability, rather than social dominance. https://doi.org/10.1101/493692

Cite the original work for its findings. Save a collection to share your selection of sources.

KEEP EXPLORING

Related preprints

Shared brain transcriptome signatures of social evolution and plasticity in shell-dwelling cichlid fishes

Inter-individual variability in phenotypic traits is widespread in nature both across and within species, with similar patterns of variation often occurring between and within species. Given that these two types of variation are generated by evolutionary and plasticity processes respectively, it raises the question to what extent the causal mechanisms underlying such variability at these two different levels are shared or not. To address this question, we studied the variation in brain transcriptomes in Tanganyikan cichlids that exhibit both intra- and interspecific variation in social behavior. We compared two facultatively social cichlid species, each containing naturally occurring solitary and social-living individuals, with a closely related obligatory solitary resembling the ancestral state. Differential gene expression and Gene Set Enrichment Analyses were performed in the telencephalon and diencephalon transcriptomes to investigate the molecular basis of both behavioral plasticity and the evolution of sociality. Behavioral plasticity involved few differentially expressed genes but extensive changes in biological pathways, supporting a highly polygenic architecture of social behavior. Across both species, social-living individuals consistently upregulated pathways involved in translation, protein homeostasis, and energy metabolism, whereas solitary individuals showed enrichment of neuronal morphogenesis, cell adhesion, and structural plasticity. Remarkably, these same functional programs were associated with the independent evolution of sociality, revealing a strong overlap between evolutionary and plastic transcriptional responses. This convergence was largely restricted to the telencephalon, while the diencephalon showed limited and inconsistent functional signatures. Together, our results support the repeated recruitment of gene regulatory programs during the evolution of sociality and demonstrate that behavioral plasticity and evolutionary transitions share common neurogenomic responses, consistent with a conserved genetic toolkit for social behavior.

animal behavior and cognition↗

Causal Multiscale Modeling of Ocular FLASH Electroretinography: Model Development, Experimental Fitting, and Spin-Glass--Percolation Predictions

\textbf{Purpose:} To develop a causal multiscale model of retinal electroretinography (ERG) after ocular ultrahigh-dose-rate (FLASH) and conventional-dose-rate (CONV) irradiation, evaluate the framework against published ocular ERG data, and derive prospective dose-response predictions for future validation. \textbf{Methods:} The retina was coarse-grained into $N=200$ functional modules. Local rate equations were formulated as Hodgkin--Huxley-inspired conductance-balance/RC reductions of retinal ion-channel and synaptic pathways. Radiation generated an injury field that altered phototransduction, a-wave and b-wave dynamics and, in the network extension, inter-module coupling and bond survival. A reduced amplitude benchmark and nested M0/M1/M2 causal models were evaluated. \textbf{Results:} The reduced benchmark achieved $R^2=0.9721$ and RMSE $=11.94~\mu$V. M0, M1, and M2 yielded $R^2=0.8546$, 0.8559, and 0.8560, respectively, indicating limited independent identifiability of the network terms from amplitude data alone. Under an exploratory 50\% retained-gain criterion, the reduced benchmark predicted a-wave preservation thresholds of 28.6 Gy for FLASH and 23.7 Gy for CONV, and b-wave thresholds of 29.2 Gy and 24.1 Gy, respectively, corresponding to a model-based functional dose-modifying factor (DMF) of 1.21. \textbf{Conclusion:} The ERG amplitude data support the causal radiation-injury-to-ERG framework, while additional observables will be needed to distinguish the predicted collective-network contributions. The model also provides quantitative dose targets for prospective studies of the FLASH retinal-preservation window and a framework for testing how local retinal injury may propagate into collective dysfunction.

animal behavior and cognition↗

Neonatal personality is associated with sex-specific developmental trajectories in a wild mammal

Animal personality, defined as consistent among-individual differences in behaviour, is an important source of phenotypic variation, but its developmental origins and associations with subsequent development remain poorly understood. We measured neonatal personalities, early-life growth, and yearling male antler length in wild fallow deer (Dama dama). Using eight years of data, we estimated repeatability and among-individual correlations among neonatal personalities and growth and applied structural equation modelling to examine associations with yearling male morphology. Heart rate and behavioural reaction measures showed repeatable among-individual variation, demonstrating that stable differences were detectable shortly after birth. Behavioural reaction was negatively correlated with growth in males but not in females. Heart rate was not associated with growth in either sex. In males, the effects of neonatal behavioural reactivity persisted beyond early life: more behaviourally reactive neonates had shorter antlers as yearlings, indirectly through reduced early-life growth. These findings show that stable among-individual differences emerge during the neonatal period and are associated with sex-specific developmental trajectories.

animal behavior and cognition↗