Method-of-moments estimators (MMEs) for the two-gene coefficients of relationship and inbreeding, and for thxe four-gene Cotterman coefficients, are described. These estimators, which use co-dominant genetic markers, are most appropriate for estimating pairwise relatedness or individual inbreeding coefficients, as opposed to their mean values in a group. This is because, compared to the maximum likelihood estimate (MLE), they show reduced small-sample bias and lack distributional assumptions. The ‘efficient’ MME is an optimally weighted average of estimates given by each allele at each locus. Generally, weights must be computed numerically, but if true coefficients are assumed zero, simplifiedestimators are obtained whose relative efficiencies are quite high. Population gene frequency is assumed to be assayed ina larger, ‘reference population’ sample, and the biases introduced by small reference samples and/or genetic drift of the reference population are discussed. Individual-level estimates of relatedness or inbreeding, while displaying high variance, are useful in several applications as a covariate in population studies.

The flanking markers of wild-type recombinant spores originating from crosses of spore colour mutants in Sordaria brevicollis were analysed. Recombinant asci were of two main types – either with one or with two wild-type spores. In most crosses the behaviour of flanking markers was significantly different for these two types of recombinant asci. The main differences were in the polarity of gene conversion (as inferred from parental outside marker combinations) and in the frequency of recombinant outside markers. These differences were interpreted in terms of hybrid DNA models of recombination and correction of heteroduplex DNA.

The recessive mutant gene downless (dl) causes abnormal texture of the coat and absence of hair on the tail. The dl locus had previously been shown to act in the epidermis and not in the dermis. To obtain evidence on the pattern of proliferation of epidermis, downless ↔ normal chimaeras were produced by embryo aggregation, and the pattern of normal and mutant hair in the coat was examined. The chimaeras showed a pattern of narrow transverse stripes of normal and abnormal hair. This pattern was similar to that found in mice chimaeric for alleles at the agouti locus known to act in the dermis. This evidence supports the conclusion that the pattern of cell proliferation is similar in dermis and epidermis, and is compatible with the hypothesis that both tissues proliferate by lateral coherent clonal growth from a randomly mixed array of longitudinally arranged cells.

A technique using microserological equipment is described whereby up to 144 quantitative interrupted bacterial matings may be performed concurrently. The technique is easy to use, accurate and reproducible, and eliminates the need for agar plates. However, it is only suitable for 40–42 °C matings and mating efficiency is approximately threefold lower than in test tubes.

Two apparently very similar quantitative characters, the numbers of hairs on the sternopleural region and on the abdominal sternites of Drosophila melanogaster, show unexpected differences in their genetic behaviour. In particular, the amount of left-right asymmetry of the sternopleurals (i.e. the mean absolute difference in numbers of hairs on the two sides of the fly) tends to decline when inbred lines are intercrossed, and can be both increased and decreased by straightforward selection; the corresponding index for the sternite hairs—the uncorrelated variance between two sternites, or the mean absolute difference between the numbers of hairs on each—appears, on the other hand, to be susceptible neither to selection nor to change when inbred lines are crossed (Mather, 1953; Reeve & Robertson, 1954; Reeve, 1959).

Weekly food intake and body weight were measured from 3 to 17 weeks of age on mice selected 14 generations for increased and decreased values of one of three criteria: appetite (A) as measured by 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 at 10 weeks of age and total lean mass (protein, P), using the index body weight in 10-week males— (8 × gonadal fat pad weight). Carcass composition analyses were undertaken on the 17-week-old mice, and are presented along with composition data for younger mice from earlier generations. The high intake A line mice are larger, eat more, have higher maintenance requirements and are slightly leaner than the low intake A line mice, but are no more efficient. The increased lean mass P line mice are much larger, eat more and are more efficient than the decreased lean mass P line mice, but show little difference in maintenance or carcass composition. The (much) fatter F line mice are larger, more efficient and eat more during the rapid growth period than their leaner F line counterparts, but show no difference in lean mass or maintenance requirements. These results provide implications about the relationships between the input (intake) and output (maintenance and lean and fat deposition) components of growth.

Cross-fertilizing stocks of Euplotes crassus, differing as to the ability to undergo autogamy, were subjected to breeding analysis. The resulting data are consistent with the interpretation that a single locus (a) with a pair of alleles (a+; a−) controls the ability to undergo autogamy. The two alleles express a simple dominance relationship in which the dominant allele (a+) permits expression of the autogamy trait. Cross-breeding experiments also suggest that the a locus is not linked to the mt locus which determines the mating-type trait.

Sex determination in Drosophila depends on the ratio of X chromosomes to sets of autosomes (X:A). This chromosomal signal is used to regulate a few control genes whose state of activity selects either the male or the female sexual pathway. We have studied the structure and function of dsx (double sex) which appears to be the last regulatory gene on whose function the sexual pathway eventually depends. We have mutagenized the locus, varied the doses of dominant dsx-mutations and wildtype alleles, and combined different dsx-alleles with recessive mutations in other sex-determining genes, such as ix, tra-2 and tra.

The locus dsx harbours two genetic functions, dsxm to implement the male program, dsxf to implement the female program. We found that dsxm and dsxf can mutate independently although most mutations abolish both functions. We conclude that dsxm and dsxf each have their specific domain, but also share a large region of DNA that is essential for both functions. We present evidence that the dominant mutations correspond to a constitutive expression of the male-determining function dsxm, with the simultaneous abolishment of the female-determining function dsxf. This effect can be counteracted by two doses of expressed dsxf so that a female phenotype results. The products of one dose of expressed dsxm and one dose of expressed dsxf in the same cell appear to neutralize each other which leads to a null phenotype. The mutant combinations suggest that the product of dsxf requires the products of ix+, tra-2+ and tra+ to become functional.

Consider a random sample of genes at a locus, drawn from a population evolving according to the infinitely many, neutral, alleles model. The sample will have a most recent common ancestor gene, which we shall call ‘Eve’. The probability distribution, for the number of genes of oldest allelic type in a sample, is known and has a neat form. Rather less is known about the distribution for the number of genes in the sample which are of the same allelic type as Eve possessed. If the latter number is positive, then these genes are automatically of the oldest type in the sample. But Eve may have no non-mutant descendants in the sample; then, the oldest allele will be a mutant arising in a line of descent after Eve. The paper studies the number of non-mutant descendants from Eve, its distribution and moments. It seems that there may be few neat results. In large samples, the proportion of genes of Eve's type has an approximate β-like density, together with a discrete probability atom at zero, if the mutation rate parameter is low. Extinction of the allele of even the population's common ancestor is possible, but not certain, and bounds are obtained for its probability. Some comments are made about the applications and implications of the results for human mitochondrial DNA.

A mutation in Escherichia coli K12 giving resistance to about 5 μg/ml of streptomycin was found to be cotransducible by P1 with proA and proB, and is located at about 8·5 min on the chromosome map. The locus is named strB. A second mutation to the same resistance level was not cotransducible with either proA or proB and must be located elsewhere. Both mutations cause a marked increase in R-factor mediated streptomycin resistance, and significant decreases in resistance to several other antibiotics, both in the presence and absence of an R-factor determinant for the same antibiotic. The two mutations differ in their effects on bacterial sensitivity to crystal violet and EDTA.

When an R determinant for streptomycin is transferred into a conditionally streptomycin-dependent E. coli B mutant—which requires in minimal medium either histidine or streptomycin—the latter behaves like a histidineless strain. This phenotype modification shows that the repairing action of streptomycin is prevented. The specific requirement of the strain is not now replaced even by streptomycin concentrations up to 10000 µg/ml at which the conditionally streptomycin-dependent mutant could originally grow, and which are well beyond the resistance level characteristic of the R determinant itself. These data seem to suggest that a reduction in permeability of the cell membrane cannot be held responsible for the phenomenon observed.

Two systems of hybrid dysgenesis, the P–M system and the I–R system, are characterized by two different specific types of non-reciprocal hybrid sterility referred to, respectively, as GD and SF sterility. In order to determine the relationship between these two systems, strains representative of the four single-system interactive types were crossed in almost all possible combinations and tested for both types of sterility. The results suggest that the two systems are at least partially independent of one another. There are several examples of single strains that contribute the maternal component for interaction in the P–M system and contribute the paternal component in the I–R system. Using parents with the potential for the two types of interaction and. appropriate temperature manipulation, both GD and SF sterility can be manifested in the same hybrid females. In other crosses, a single type of sterility is observed, or none at all, according to the dual designation of the parental strains. The evidence from a number of additional crosses suggests that most strains of this species have the potential for both types of interaction to varying degrees when mated in appropriate combinations. Some theoretical and practical implications of these results are discussed.