The esterase 6 (Est-6) locus in Drosophila melanogaster is located on the third chromosome and is the structural gene for a carboxylesterase (E.C.3.1.1.1) and is polymorphic for two major electromorphs (slow and fast). Isogenic lines containing X chromosomes extracted from natural populations and substituted into a common genetic background were used to detect unlinked factors that affect the activity of the Est-6 locus. Twofold activity differences of esterase 6 (EST 6) were found among males from these derived lines, which differ only in their X chromosome. These unlinked activity modifiers identify possible regulatory elements. Immunoelectrophoresis was used to estimate quantitatively the levels of specific cross-reacting material in the derived lines. The results show that the variation in activity is due to differences in the amount of EST 6 present. The data are consistent with the hypothesis that there is at least one locus on the X chromosome that regulates the synthesis of EST 6 and that this regulatory locus may be polymorphic in natural populations.

The shape of the mandible of the mouse can be described by a series of discriminant functions which have been used to discriminate between and investigate relationships among strains of mice. The effect of sex and variation in age of the animal on the results obtained from these functions has been investigated. Significant sex differences in mandible shape were detected, but these were considerably smaller than the differences found between two inbred strains. A simple correction for expressing each measure as a proportion of the sum of the measures on each bone removes the effects of overall size. Significant age effects were found, but these were only large in animals under seven weeks of age where considerable changes are taking place in the relative lengths of bone measurements. Routine testing for genetic authenticity using the shape of the mandible is possible over a wide age range and may be an efficient method for monitoring genotypes at the end of long-term experiments.

Genetic variation in the modulating effect of dietary sucrose was assessed in Drosophila melanogaster by examining 27 chromosome substitution lines coisogenic for the X and second chromosomes and possessing different third isogenic chromosomes derived from natural populations. An increase in the concentration of sucrose from 0·1% to 5% in modified Sang's medium C significantly altered the activities of 11 of 15 enzyme activities in third instar larvae, indicating that dietary sucrose modulates many, but not all, of the enzymes of D. melanogaster. A high sucrose diet promoted high activities of enzymes associated with lipid and glycogen synthesis and low activities of enzymes of the glycolytic and Krebs cycle pathways, reflecting the physiological requirements of the animal. Analyses of variance revealed significant genetic variation in the degrees to which sucrose modulated several enzyme activities. Analysis of correlations revealed some relationships between enzymes in the genetic effects on the modulation process. These observations suggest that adaptive evolutionary change may depend in part on the selection of enzyme activity modifiers that are distributed throughout the genome.

Two mouse populations, randombred albino mice and a cross of four inbred strains, were divergently selected for high (H8) and low (L8) 8-week body weight over 18 generations using within-family and individual selection. The crossbreds showed asymmetry of selection response and realized heritabilities (H8 0·29 ± 0·01; L8 0·17 ± 0·01). In the randombred population realized heritabilities were symmetrical (H8 0·23 ± 0·01; L8 0·22 ± 0·02). Over the first nine generations individual selection was nearly 40 per cent better than within-family selection, as was expected from the full sib correlation in both populations. As selection progressed, within-family selection reached 82% and 61% of the responses obtained with individual selection in the crossbreds and randombred respectively. Correlated responses for 3-week (weaning) and 5-week body weights agreed with observations made on direct responses, but selection for L8 did not reduce weaning weight. Selection for L8 decreased and selection for H8 increased first litter size at birth. However, mass-selected L8-pairs had a higher life-reproduction and life-span than H8-pairs.

Mice were selected for one of three criteria: appetite (A), measured as 4- to 6-week food intake, adjusted by phenotypic regression to minimize change in 4-week body weight, fat percentage (F), using the ratio of gonadal fat pad weight to body weight in 10-week-old males, and total lean mass (protein, P), using the index, body weight in 10-week-old males − (8 × gonadal fat pad weight). For each selection criterion, there were 3 high, 3 low and 3 unselected control lines. At generation 11, the high and low A lines diverged by 17% of the control mean and the realized heritability from within family selection of adjusted food intake was 15%. Selection for this character produced changes in body weight, gross efficiency from 4 to 6 weeks, and percentage of fat, the high lines being heavier, more efficient and less fat than the lows. The high and low F lines diverged by 80% of the control mean and the realized heritability of the ratio of gonadal fat pad weight to body weight was 44%. Selection for this character produced changes in total fat per cent, but little change in percentage protein, body weight, food intake or gross efficiency. The high and low P lines diverged by 40% of the control mean and realized heritability of the lean mass index (10-week weight − [8 × gonadal fat pad weight]) was 51%. Selection for an increase in the index increased body weight at all ages, food intake and 4- to 6-week gross efficiency. There was no change in percentage fat. Responses in the selected traits were not highly correlated, and the different lines provide an opportunity for investigating responses in physiology, metabolism and gene products.

The partitioning of digestible energy intake on an ad libitum diet of standard mouse nuts was investigated in mice selected for high and low body weight at eight weeks and in an unselected control population. In selected mice aged from four to six weeks and housed at a temperature of 24·5 °C, almost all their energy intake could be attributed to basic maintenance and the deposition of extra protein and fat. Control mice, however, had an energy intake considerably in excess of their apparent maintenance and growth requirements. It was concluded that the unaccountable energy loss of the control line could be used to increase growth efficiency in the selected lines. The result is analogous to those obtained from studies on normal and obese mouse genotypes and indicates genetic changes in mechanisms controlling the conversion of food energy to heat.

Provision of a nest to reduce thermoregulatory heat production caused a minor reduction in energy intake and a corresponding decrease in the energy discrepancy. There was no effect on growth.

The Ybb− chromosome has been previously shown to induce reduction of X chromosome ribosomal genes in Xbb / Ybb− or Xbb+ / Ybb− flies. These reduction events are presumed to arise as one of the two products of unequal sister chromatid exchanges, which result in both magnified and reduced products. Bobbed reduced chromosomes may also arise as products of other recombinative events such as intrachromatid deletions. In this report we use the Ybb− chromosome to reduce the number of ribosomal genes present on X chromosomes from two wild-type stocks under ‘non-magnifying’ conditions. We then show that the bobbed reduced X chromosomes show no detectable difference in their Southern blot rDNA patterns when compared with the parental wild-type X chromosome. This indicates that reduction events do not preferentially delete certain repeat classes, and supports previous observations that the repeat types present in the D. melanogaster X chromosome nucleolus organizer are not significantly clustered.

Nine diverse lines of cultivated barley (Hordeum vulgare) and 11 lines of its wild progenitor (H. spontaneum) were assayed for variation in their chloroplast DNA by digestion with ten restriction endonucleases. The cultivated lines exhibited a single cpDNA polymorphism, whereas the wild material exhibited five. The significantly lower level of diversity among the cultivated lines was unexpected because both cultivated and wild lines had been selected for comparable levels of diversity for nuclear encoded isozyme loci. These results suggest that the level of cytoplasmic diversity was markedly restricted during the domestication of cultivated barley.