Genetic influences on digging behaviors in mice (Mus musculus) in laboratory and seminatural settings

Digging behaviors of several inbred strains of laboratory mice and some of their crosses were examined in three contexts. In laboratory burrow boxes, C57BL/6Abg mice constructed more sophisticated burrow systems than did BALB/cAbg mice. Their F1 hybrids built burrow systems more complex than either parental strain. The same pattern of genetic influence was observed in an outdoor pen. In an escape task that required digging, BALB/c mice escaped more quickly than did C57BL/6 mice; their F1 hybrids showed dominance toward the BALB/c phenotype. These results indicate that behavioral polymorphisms in digging behavior, which may relate to habitat selection, have a genetic basis. The dominance and overdominance toward the better digging parental strain in each type of task suggest the possible evolutionary importance of these digging behaviors.     

Genetic and environmental influences on behavior: capturing all the interplay

Basic quantitative genetic models of human behavioral variation have made clear that individual differences in behavior cannot be understood without acknowledging the importance of genetic influences. Yet these basic models estimate average, population-level genetic and environmental influences, obscuring differences that might exist within the population and masking systematic transactions between specific genetic and environmental influences. This article discusses a newer, more sophisticated and powerful quantitative genetic model that articulates these transactions. Results from this model highlight the ways in which the gene- environment interaction and correlation are intertwined. They can be used to integrate findings from quantitative and molecular genetic studies and to understand the roles of genetic influences and social forces in manifested behaviors, even when DNA sequence variation is not relevant.     

Pavlovian influences on goal-directed behavior in mice: the role of cue-reinforcer relations

Two experiments refined procedures to study Pavlovian influences on goal-directed behavior in mice and studied the effects of CS-US relations in Pavlovian-instrumental interactions. Independent groups of mice underwent Pavlovian training to associate either a 10-sec or 2-min auditory stimulus (CS) with reward. We next assessed the ability of the response-contingent CS presentations to reinforce novel instrumental responding (conditioned reinforcement; CRf) or the ability of noncontingent CS presentations to increase ongoing instrumental responding (Pavlovian-instrumental transfer; PIT). Whereas 10-sec training conditions produced strong CRf (and no PIT), 2-min training conditions produced robust PIT (but no CRf).     

Genetic and experiential influences on behavior: Twins reunited at seventy-eight years

Twins living in different countries offer opportunities to explore associations between observed differences and experiential effects. This report compared the life histories, cognitive abilities, personality traits, psychomotor skills, medical characteristics, job satisfaction, social support and social relations of dizygotic (DZ) female twins reunited at 78, the world’s longest separated set. The twins’ advanced age also enabled a study of how co-twin differences in aging may be associated with current behavioral and social differences. Consistent with previous studies, these dizygotic reared apart (DZA) twins showed discordance across some, but not all, traits. Their different rearing situations and life histories may explain current differences in their responses to meeting their twin. This case highlights the importance of both genetic and rearing factors on behavior, but does not allow firm conclusions regarding the extent to which these sources explain individual developmental differences. However, such data contribute to the growing number of cross-culturally separated twins, generating novel hypotheses that may be assessed using larger samples.     

Genetic influences on the overlap between low IQ and antisocial behavior in young children

The well-documented relation between the phenotypes of low IQ and childhood antisocial behavior could be explained by either common genetic influences or environmental influences. These competing explanations were examined through use of the Environmental Risk Longitudinal Twin Study 1994-1995 cohort (Moffitt & the E-Risk Study Team, 2002) of 1,116 twin pairs and their families. Children's IQ was assessed via individual testing at age 5 years. Mothers and teachers reported on children's antisocial behavior at ages 5 and 7 years. Low IQ was related to antisocial behavior at age 5 years and predicted relatively higher antisocial behavior scores at age 7 years when antisocial behavior at age 5 years was controlled. This association was significantly stronger among boys than among girls. Genetic influences common to both phenotypes explained 100% of the low IQ-antisocial behavior relation in boys. Findings suggest that specific candidate genes and neurobiological processes should be tested in relation to both phenotypes.     

Assimilative behavior identification can also be resource dependent: the unimodel perspective on personal-attribution phases

Three studies examine the role of situational constraint information on behavior identification. It was found that where the behavior-identification task is relatively easy assimilation of the behavior-identification to situational constraints is independent of cognitive load. However, where the behavior-identification task is relatively difficult, assimilation is undermined by load. Given that the discounting of situational constraint information, too, can be independent of load where the dispositional-inference task is easy, and is load-dependent when the task is difficult, it appears that both assimilation and discounting behave identically in regard to load. This conclusion is consistent with the judgmental unimodel whereby behavior identification and dispositional inference differ in the contents of the judgmental questions they address while sharing the underlying process whereby these questions are answered.     

Genetic and environmental influences on antisocial behavior: a meta-analysis of twin and adoption studies

A meta-analysis of 51 twin and adoption studies was conducted to estimate the magnitude of genetic and environmental influences on antisocial behavior. The best fitting model included moderate proportions of variance due to additive genetic influences (.32), nonadditive genetic influences (.09), shared environmental influences (.16), and nonshared environmental influences (.43). The magnitude of familial influences (i.e., both genetic and shared environmental influences) was lower in parent-offspring adoption studies than in both twin studies and sibling adoption studies. Operationalization, assessment method, zygosity determination method, and age were significant moderators of the magnitude of genetic and environmental influences on antisocial behavior, but there were no significant differences in the magnitude of genetic and environmental influences for males and females.     

The development of territorial-induced intermale agonistic behavior in albino laboratory mice

Male mice of the CF-1 strain (Mus musculus) were allowed to take up lone residence in a small territory consisting of a 60-cm enclosure attached by a tubular runway to a standard mouse cage with food, water, and bedding. A group of ten mice, each of which resided in its own separate enclosure for 24 hours, were more aggressive toward intruders than other groups of ten mice following six-hour residence periods, or no such residence. Aggression toward intruders increased in repeated weekly tests of the six-hour residents, but after four weeks of testing did not reach the maximum stable level displayed by the 24-hour residents over four weeks of testing. In another experiment, the 24-hour residence period of groups of 20 CF-1 male mice was disturbed by briefly removing the mouse from the enclosure, before introducing the intruder, at various intervals prior to testing. Removal of the resident five minutes before testing resulted in a marked decrease in aggression toward intruders. Although lesser decreases in aggression followed intervals of 30, 45, and 60 minutes, a 180 minute interval resulted in no appreciable effects compared to undisturbed controls. It is concluded that exposure to the stimuli provided by the enclosure results in an aggressive readiness in the resident mouse which reaches a high level within a 24-hour period.     

Observational learning in mice can be prevented by medial prefrontal cortex stimulation and enhanced by nucleus accumbens stimulation

The neural structures involved in ongoing appetitive and/or observational learning behaviors remain largely unknown. Operant conditioning and observational learning were evoked and recorded in a modified Skinner box provided with an on-line video recording system. Mice improved their acquisition of a simple operant conditioning task by observational learning. Electrical stimulation of the observer's medial prefrontal cortex (mPFC) at a key moment of the demonstration (when the demonstrator presses a lever in order to obtain a reward) cancels out the benefits of observation. In contrast, electrical stimulation of the observer's nucleus accumbens (NAc) enhances observational learning. Ongoing cognitive processes in the demonstrator could also be driven by electrical stimulation of these two structures, preventing the proper execution of the ongoing instrumental task (mPFC) or stopping pellet intake (NAc). Long-term potentiation (LTP) evoked in these two cortical structures did not prevent the acquisition or retrieval process--namely, mPFC and/or NAc stimulation only prevented, or modified, the ongoing behavioral process. The dorsal hippocampus was not involved in either of these two behavioral processes. Thus, both ongoing observational learning and performance of an instrumental task require the active contribution of the mPFC and/or the NAc.     

Adrenocortical influences on free-operant avoidance behavior

Rats were conditioned to avoid shock on a free-operant avoidance schedule in which no exteroceptive stimulus signaled impending shock. Injections of adrenocorticotropic hormone (ACTH) or dexamethasone raised blood levels of glucocorticoids. These increases were accompanied by changes in avoidance performance: there was a higher frequency of long-duration interresponse times, a greater stability among them, and fewer short interresponse times, total responses, and shocks.     

Extinction can be enhanced by a concurrent excitor

Five experiments used rat subjects to investigate the impact on extinction of the presence of other conditioned stimuli. In Experiments 1 (Pavlovian magazine approach) and 2 (instrumental discriminative training), an excitatory stimulus (X) was extinguished alone, in conjunction with a previously reinforced other stimulus (A), in conjunction with previously nonreinforced other stimulus (B), or it was spared extinction. Responding during extinction was greatest to AX, and subsequent testing of X alone showed AX extinction to have produced the most decrement to X. Experiment 3 found similar results using a within-subject design. Experiment 5 continued separate reinforced presentations of A during extinction. This procedure not only promoted extinction of X but also converted it into a conditioned inhibitor. These experiments bear on the mechanisms of overshadowing and stimulus processing, as well as provide information on the determinants of extinction.     

Genetic and environmental influences on person-situation interactions

Genetic and environmental influences on person-situation and person-mode of response interactions for anxiety and for dominance were investigated in an adult twin sample. For anxiety, evidence of significant genetic variance was found for the person-situation interaction and the person-mode of response interaction. For dominance, evidence of shared sibling-environmental influences was found for the person-situation interaction. Sex differences in the patterns of findings were also examined. The data indicate that the factors influencing personsituation interactions vary depending on the specific trait studied, and the results provide empirical support for the “interactionist” hypothesis that an individual's behavior can be characterized by meaningful patterns of behavior across situations. In addition, the study illustrates that behavior-genetic research can be designed to address important theoretical questions about the nature of personality.     

The role of endocrines in isolation-induced lntermale fighting in albino laboratory mice. II. Sex steroid influences in aggressive mice

Isolation-induced intermale fighting in laboratory mice can be dramatically reduced under most circumstances by castration. This behavior in castrates may, however, be restored, or even accentuated, by androgen replacement. Experiments on the effects of sex steroids on such fighting in castrated mice, which, for want of a better term, are designated as “aggressive,” have been recently described. These mice are housed with a female until 10 days after siring a litter and are, thereafter, housed individually for a further 14 days before castration and subsequent hormone treatment. Such mice show substantial levels of fighting in “standard-opponent” tests even before isolation. Although castration results in reduced fighting in these mice, this behavior is rarely completely abolished in all individuals. It seems likely that steroid treatment of aggressive mice maintains or intensifies an already present motivation. Treatments in these studies consisted of daily oil-based intramuscular injections for 14 days preceding and throughout behavioral testing. The standard-opponent tests were 7 min encounters with adult, subordinate, grouped males in the cleaned home cages of experimental mice. The steroids investigated included estradiol benzoate (EB), 19-hydroxytestosterone (19-OHT), androstenedione (A), testosterone (T), and Sα-dihydrotestosterone (DHT), either singly or in combination. The results suggest that (a) on a dosage basis, estrogens were at least as effective as androgens in maintaining fighting in castrated aggressive mice; (b) 19-OHT (one of the metabolic intermediates between testosterone and 17 β-estradiol) was also effective but somewhat less so than the same dose of EB; (c) the three naturally occurring androgens investigated all effectively maintained fighting at comparatively low doses (50 μg/day) which compares with a replacement dose of 500 μg/day of T in some studies in traditional castrated mice (e.g., Luttge and Hall, 1973); (d) aromatization is not essential for a behavioral action of androgens as DHT, a nonaromatizable androgen, maintained fighting in these mice; (e) whereas a two-site (central motivational and peripheral penile) action seems probable in the influence of androgens on sexual behavior in castrated rats (e.g., Parrott, 1975), DHT did not augment the action of EB on fighting in castrated aggressive mice, indicating that only a central action of steroids was required in the aggressor.     

Genetic influences on the development of spatial skills during early adolescence

The course of development of skill at face encoding is disrupted in early adolescence. Evidence is provided that the timing of this disruption is under genetic control. Regardless of their age, girls in the midst of pubertal change encode faces less efficiently than prepubescent or postpubescent controls. This maturational influence on face encoding is contrasted with a different effect of pubertal development on another visuo-spatial ability, performance on the Embedded Figures Test (EFT). Regardless of their pubertal status at time of testing, girls who mature earlier are disadvantaged on EFT compared to those who mature later. The results for EFT replicate earlier findings on the relation between individual differences in the age at which adolescence begins and certain spatial skills. Several possible explanations for each of these effects—that of maturational status on face encoding and that of maturation rate on EFT—are discussed. Consideration of the relation between physical and mental growth is advocated as a source of constraints on explanations of cognitive development.     

Genetic and environmental influences on adult attachment styles

The heritability of adult attachment styles as measured by the Relationship Scales Questionnaire (RSQ) was estimated on data from a volunteer general population sample of 220 adult twin pairs (116 monozygotic pairs. 104 dizygotic pairs). Additive genetic effects accounted for 37%, 43%, and 25% of the variance in the secure, fearful, and preoccupied adult attachment styles, respectively, but none of the variance in the dismissing style. Nonshared environmental influences accounted for the majority of the variance in all styles: 63% secure, 57% fearful, 75% preoccupied, and 71% dismissing. Shared environmental effects were negligible for all styles except dismissing (29%).