Genetic analysis of laterality in house mice (Mus musculus L.)

An attempt was made to obtain with the help of selection-genetic method, mice lines with genetically determined differences in lateralization of the fore-legs (right-, left-handedness). In 5 generations of selection, 302 animals-offsprings were studied, obtained through crossing of the lines CBA X C57BL/6. Two parameters of asymmetry were investigated: direction and degree. It is shown that the genotype controls the degree of the lateralization of the fore-legs, whereas the direction of lateralization is not subjected to a rigid genetic control. In the studied mice population, "right-handed" mice prevail over "left-handed" ones, which seems to be due to their dwelling conditions in the early ontogenesis.     

Induction of dominant lethals in progeny of male CBA mice after pheromonal action

The inhibiting effect of pheromone 2,5-dimethylpyrazine of house mouse females on the reproductive function of the CBA male mice was studied. The mutagenic effect of six-day pheromonal effect was assessed by dominant lethal test. Analysis for the frequency of dominant lethals showed that the pheromonal effect results in an increased death rate of the progeny of the treated males. This is probably explained by implantation failure and is expressed in a reduced average number of the implantation sites and low live embryos per female. The proportion of females with live embryos decreased significantly. The implication of the effect of female mouse pheromone 2,5-dimethylpyrazine on the genetic processes in germ cells of male mice is discussed.     

Aggressive behaviour in related and unrelated wild house mice (Mus musculus L.)

Aggressive behaviour was observed to be rare in small family groups of confined wild house mice, Mus musculus L. Unrelated mice were attacked when they were introduced to a family group and in their presence intra-family aggressive behaviour increased. When two family groups of mice were allowed to meet there were frequent aggressive encounters between unrelated animals and the two groups remained separate. Resident mice were found to be aggressive towards males and females individually isolated and returned to their own family after 2 or 3 weeks absence but not after 1 week. The possibility is discussed that in wild mice odour discrimination influences the dispersal and build-up of free-living populations.     

Testosterone rapidly reduces anxiety in male house mice (Mus musculus)

Eight experiments supported the hypotheses that reflexive testosterone release by male mice during sexual encounters reduces male anxiety (operationally defined in terms of behavior on an elevated plus-maze) and that this anxiolysis is mediated by the conversion of testosterone to neurosteroids that interact with GABA(A) receptors. In Experiment 1, a 10-min exposure to opposite-sex conspecifics significantly reduced both male and female anxiety 20 min later (as indexed by increased open-arm time on an elevated plus-maze) compared to control mice not receiving this exposure. In contrast, locomotor activity (as indexed by enclosed-arm entries on the elevated plus-maze) was not significantly affected. The remaining experiments examined only male behavior. In Experiment 2, exposure to female urine alone was anxiolytic while locomotor activity was not significantly affected. Thus, urinary pheromones of female mice likely initiated the events leading to the male anxiolysis. In phase 1 of Experiment 3, sc injections of 500 microg of testosterone significantly reduced anxiety 30 min later while locomotor activity was not significantly affected. Thus, testosterone elevations were associated with reduced male anxiety and the time course consistent with a nongenomic, or very rapid genomic, mechanism of testosterone action. In phase 2 of Experiment 3, the anxiolytic effect of testosterone was dose dependent with a 250 microg sc injection required. Thus, testosterone levels likely must be well above baseline levels (i.e., in the range induced by pulsatile release) in order to induce anxiolysis. In Experiment 4, a high dosage of 5alpha-dihydrotestosterone was more anxiolytic than a high dosage of estradiol benzoate, suggesting that testosterone action may require 5alpha-reduction. In Experiments 5 and 6, 3alpha,5alpha-reduced neurosteroid metabolites of testosterone (androsterone and 3alpha-androstandione) were both anxiolytic at a lower dosage (100 microg/sc injection) than testosterone, supporting the notion that testosterone is converted into neurosteroid metabolites for anxiolytic activity. Experiments 7 and 8 found that either picrotoxin or bicucculine, noncompetitive and competitive antagonists of the GABA(A) receptor, respectively, blocked the anxiolytic effects of testosterone. However, conclusions from these 2 experiments must be tempered by the reduction in locomotor activity that was also seen. The possible brain locations of testosterone action as well as the possible adaptive significance of this anxiolytic response are discussed.     

Urine marking and social dominance in male house mice (Mus musculus domesticus)

House mice use urine marking for a variety of forms of social communication. Urine marking varies with dominance status; socially dominant male house mice urine mark more than those that are socially subordinate. Experiment I was designed to confirm this previous finding. Experiment II was designed to test whether urine marking, measured prior to testing males for aggression, could be used to predict social dominance. Mice were tested for urine marking in 20 cmx40 cm rectangular cages with filter paper below the wire mesh bottom of the cage. In Experiment I, groups of four males were tested in a round robin design to assess social dominance and were then placed individually in urine marking cages. Social dominance was a significant predictor of the number of 1 cm squares that contained urine marks, both with regard to interior squares and for perimeter squares in the test cage. In Experiment II, groups of four males were first tested individually in urine marking cages and then used for round robin aggressive encounters to assess social dominance. The number of interior squares with urine marks, and, to a lesser extent, the number of perimeter squares with urine marks, were both significant predictors of aggression scores and social dominance status. Being able to judge social dominance without having the mice encounter each other could be a valuable tool for future work; confounding effects on such parameters as hormone levels could be avoided while obtaining an estimate of male social dominance status.     

Differences in aggressive behaviour between male mice (Mus musculus L.) in colonies of different sizes

Using cages of uniform size, colonies of three, four, five, nine and twelve unfamiliar male mice were established and observed over a 21-day period. A dominant mouse emerged in every colony, but in the two largest sizes five to six changes in dominance were recorded. The per capita aggression did not increase with colony size. There was a general linear decline in the number of attacks recorded in colony sizes nine and twelve whilst in the three smaller colony sizes the dominant showed an exponential decline in aggressiveness. Differences in hierarchical organization were interpreted in terms of the number of attacks shown by the dominant in relation to the number of subordinates present.     

Antimutagenic effect of chemosignals from isolated female house mouse on male germ cells (Mus musculus L.)

The influence of chemosignals from isolated mature females of the CBA strain on level of spontaneous and radiation-induced meiotic disturbances in spermatocytes I of males of the same strain was studied. Using an ana-telophase method, 24-hour exposure of males to soiled bedding containing isolated females’ chemosignals was shown to lead to a significantly lower frequency of chromosomal aberrations and other meiotic disturbances in spermatocytes I as compared to males kept on clean bedding. The same effect of female chemosignals was found in the germ cells of irradiated males (4 Gr). The mechanisms and importance of the revealed antimutagenic effect of mouse female chemosignals on the male reproductive cells in the reproduction process are discussed.     

Studies of the induction of dominant lethals and translocations in male mice after chronic exposure to microwave radiation

Male C3H mice were exposed to 100 W m-2 of 2.45 GHz continuous-wave microwave radiation for 6 h per day for a total of 120 h over an 8-week period. The exposure level was chosen so that the specific energy absorption rate (SAR) would be approximately equal to the level of 4 W kg-1 which is considered by a number of organizations to be a threshold for adverse biological effects. At the end of the treatment period the mice were mated with a different group of (C3H x 101) F1 hybrid females each week for the following 8 weeks. There was no significant reduction in pregnancy rate, preimplantation survival or postimplantation survival in the exposed group compared to sham-exposed controls. At the end of the mating period a cytogenetic analysis was carried out of meiotic chromosome preparations of testicular tissue, thus sampling cells that were stem cell spermatogonia during the treatment regime. The results showed no difference in the frequency of reciprocal translocations between the sham and treated groups, or in the frequency of cells with autosome or sex chromosome univalents. Low levels of fragments and exchanges were found in both groups. It is concluded that there is no evidence in this experiment to show that chronic exposure of male mice to 2.45 GHz microwave radiation induces a mutagenic response in male germ cells. This conclusion is in agreement with the observations of Berman et al. (1980), who reported a lack of male germ cell mutagenesis after repetitive or chronic exposure of rats to 2.45 GHz.     

Polymeric hemoglobins of the house mouse (Mus musculus L.): Isolation of cysteinyl peptides

Hemoglobins from wild populations of the house mouse (Mus musculus L.) are polymorphic with respect to the diffuse or single appearance of their electrophoretic patterns and their ability to form polymers. Polymerization occurs by the formation of intermolecular disulfide bonds. Isolation of all the cysteinyl peptides shows that the reactive cysteinyl residue, 13, is in the same position as that found in BALB/cJ laboratory mice.This research was supported in part by grant F-213 from the Robert A. Welch Foundation, and NIH grants GM-05818 and GM-09326, and an NIH predoctoral fellowship to J. B.     

Differential response to the odor of familiar intruder mice in male mice (Mus musculus)

Responses to the odor of familiar intruder male mice according to their dominance were investigated. Responses were classified into 2 aspects: the investigation of the odor and the decision-making regarding avoiding it or not. The results varied according to the dominance of the respondents and the odor donor, and also according to the context of previous encounter situations. The dominants that had attacked an intruder dominant mouse responded randomly to its odor, whereas the dominants that had fought with it tended to avoid the odor. The subordinates that had observed an intruder dominant mouse being attacked by its dominant cagemate preferred the passage with the intruder's odor. The odor of a subordinate mouse was neither avoided nor preferred by either the dominants or subordinates. It was suggested that mice distinguished the dominance of the odor donor regardless of the context of the previous encounter situation, but they responded differently according to it and also according to their own dominance status.     

A quantitative study of the second meiotic metaphase in male mice (Mus musculus).

Over 11,000 second meiotic metaphase spreads stained for the pericentromeric region have been studied quantitatively in male mice of 14 strains. The sex-chromosome constitution of a cell could be judged objectively if X and Y chromosomes and ploidy were all scored. A bias arose if only Y chromosomes and ploidy were scored but could be corrected statistically. There was no sign of other forms of bias. The original contiguity of X and Y second metaphases in vivo was very occasionally evident in the preparations. Most of the subhaploid aneuploid counts were assumed to be artifactual. The incidence of truly aneuploid second metaphases in 13 strains was estimated as 0.38+/-0.12%. The estimated average rate per chromosome was 0.019+/-0.006%, with a comparable order of magnitude for the sex chromosomes alone. Simultaneous aneuploidy of two or more chromosomes of the haploid set was estimated to be very rare. Of the spreads from 13 strains, 9.6% were polyploid (2N, 3N, 4N) and showed most of the possible combinations of sex chromosomes. Nearly all the polyploid spreads were considered to arise by artifactual cell fusion at the time of second metaphase during the preparative technique, especially of the X and Y daughter-cell products of the first meiotic division. Other modes of origin (true polyploidy, accidental superposition of cells during preparation) were unlikely. The data could be accommodated by a statistical model with only four parameters. It allowed for artifactual fusion mainly between daughter cells but also between non-daughter cells, bias in one scoring method, and bias in the numbers of cells with given ploidy successfully mounted. Current techniques of chromosome preparation were thought to be wholly unsuitable for the recognition of true polyploidy. The artifactual origin of polyploid spreads was borne out by an absence of polyploid spermatozoa in 14 strains. There appeared to be a virtually constant transmission rate of paternal X and Y chromosomes from early meiosis to late blastocyst. The estimated rate of 49.05+/-0.67% with a Y chromosome also estimated the primary sex ratio. There was evidence of polymorphism in autosomal pericentromeric staining in 3 strains. No measure of the numbers of autosomes or sex chromosomes varied significantly between duplicate preparations or between duplicate males of a strain.     

Action of two pyrazine-containing chemosignals on cells of bone marrow and testes in male house mouse Mus musculus L

Evolutionary conservative chemosignal 2,5-dimethylpyrazin that is pheromone in female mice has been shown to increase frequency of mitotic aberrations analyzed with aid of metaphasic and ana-telophasic analysis in bone marrow cells. Replacement of one of methyl radicals in the pheromone molecule by the carboxyl radical reveals specificity of action of the used derivative: the frequency of disturbances revealed only by the ana-telophasic analysis increases, whereas by the metaphasic analysis, no induction of disturbance is detected. In the sperm head abnormality test there is shown a rise of the anomalies by both compounds. Possible mechanisms of specific action of the tested substances on stability of genetic apparatus of the bone marrow dividing cells in the house mouse are discussed.