Isoenzymes of alcohol (ADH), malate (MDH), glutamate (GDH) and isocitrate (IDH) dehydrogenases, and a fast migrating esterase (EST-l) were separated by disk electrophoresis from dry seed extracts of diploid, tetraploid, hexaploid and octaploid species or amphiploids belonging to the subtribe Triticinae. Only ADH and EST-l isoenzymes showed inter-species variation; the other dehydrogenases, which show stringent substrate specificities (‘critical’ enzymes), revealed the same pattern in all diploid and polyploid species. The qualitative zymogram studies showed that (1) the number of variant enzyme bands increased with the level of ploidy, (2) the amphiploid isoenzyme pattern was additive of the parental species, (3) enhancement in the number of bands was due to the presence of not only parental bands, but also hybrid bands formed by association between heteromonomers. Quantitative data were obtained by densitometry of the enzyme bands as well as spectrophotometric measurements of enzyme activity in crude extracts. Increase in the level of enzyme activity was observed with ploidy level. In spite of the evidence that all duplicate/triplicate genes are expressed, increased enzyme activity observed in the polyploid species was not proportional to the level of ploidy or expected gene dosage. On the basis of ADH and EST-l zymograms obtained in 2 × and 4 × wheat, probable zymograms for these enzymes in the B-genome donor to 4 × wheat were extrapolated. Neither Ae. speltoides nor Ae. bicornis showed the extrapolated ADH pattern. Amphiploids involving Ae. speltoides and Triticum monococcum or T. aegilopoides fully reproduced the EST-l zymogram of 4 × wheat, but not the ADH. Ae. bicornis × T. aegilopoides amphiploid showed an ADH zymogram similar to that of 4 × wheat, but the EST-l bands were different.

The contribution of maternal and foetal genotype to the regulation of extra-embryonic (exocoelomic and amniotic) fluid and embryonic fluid in the mouse is discussed. Three of the four inbred strains studied (A, BALB/c and CBA) had similar patterns of fluid accumulation. The fourth (C57BL) differed significantly. In the reciprocal F1 crosses between CBA and C57BL a maternal effect was present. In the F2 no increase in variance of extra-embryonic fluid was noted.

The effects of two mutant genes were studied. Blebs (my) had no effect on the total fluid in the conceptus, but led to a rearrangement of fluid within the embryo. Brachyphalangy (Xtbph) caused an overall increase in fluid within the conceptus. Distribution of the excess depended upon the phenotype (exencephalic versus non-exencephalic) of the embryo.

Mutants of Pseudomonas aeruginosa isolated as being resistant to p-fluorophenylalanine (FPA-r) are pleiotropic, showing patterns of phenotypic alteration of host-controlled modification, growth rate at 37 and 43 °C, ability to grow on minimal medium, response to antibiotics and ribosomal characteristics. Alterations in host-controlled modification are also found in FPA-r mutants of Escherichia coli B.

The pleiotropy arising in these FPA-r mutants of P. aeruginosa appears to result from alterations in the specificity of protein synthesis. Phenotypic variations in host-controlled modification of the type found in the FPA-r mutants may provide a method for the detection of suppressor mutations which act by miscoding.

An investigation was made of the chromosomal position of the mutant locus, in Mutant 10/13 of Triticum aestivum (2n = 6x = 42), affecting homoeologous chromosome pairing at meiosis. In hybrids between Mutant 10/13 and rye (Secale cereale 2n = 14), homoeologous chromosomes frequently pair at meiosis although normally, in wheat-rye hybrids, this happens infrequently.

The association of the mutant condition with chromosome 5B was determined by (i) the absence of segregation in hybrids obtained when Mutant 10/13 monosomic 5B was pollinated by rye; (ii) the occurrence of trisomie segregation for pairing behaviour in 28-chromosome wheat-rye hybrids, obtained from SB trisomie wheat parents with two 5B chromosome from a non-mutant and one from a mutant parent; (iii) the absence of segregation for pairing behaviour in the 29-chromosome wheat-rye hybrids obtained from the same trisomie wheat parents.

The alternative pairing behaviours segregated independently of the centromere when wheat plants that were simultaneously heteromorphic, 5BL telocentric/5B complete, and heterozygous for the Mutant 10/13 state, were pollinated by rye. The alternative chromosome-pairing patterns segregated to give a ratio not different from 1:1, so that the association of homoeologous pairing with Mutant 10/13 probably derived from the occurrence of mutation at a single locus on 5BL. In the disomic heteromorphic state, 5BL was 91 map units in length.

Trisomie wheats with two complete 5B chromosomes and one 5BL telocentric, that were also heterozygous for the Mutant 10/13 condition, were pollinated by rye. Among the resulting 28-chromosome hybrids there was a 2:1 segregation of hybrids with low pairing: high (homoeologous) pairing and also of hybrids with complete 5B: telocentric 5BL. However, there was no evidence of linkage in this trisomie segregation. All the 29-chromosome hybrids from this cross had low pairing and it could be concluded that the single mutant allele, in Mutant 10/13, was recessive. In the trisomie condition, relative to a simplex situation, 5BL was 33·05 map units in length.

The critical locus on 5BL was designated Pairing homoeologous. The normal dominant allele was symbolized Ph and the recessive allele, in Mutant 10/13, ph.

The prevention of homoeologous pairing by the activity of a single locus makes the evolution of the regular meiotic behaviour of T. aestivum more readily comprehensible.

Multiple recombinational events within a gene were studied by tetrad analysis of multipoint intragenic crosses. It was found that a considerarle proportion of double-site conversions can arise as two separate but correlated events. The same was true for conversion and crossing-over associated with it. The data point to a possibility of multiple recombinational events involving both conversions and cross-overs, occurring as successive rounds of recombination within a single recombinational process. Some of the results suggest that more than two chromatids may be involved in such a process. The results are discussed in terms of different recombination models.

The glucose analogue 2-deoxy-D-glucose seriously inhibits the growth of Coprimts lagopus. Following treatment with N-methyl-N′-nitro-N-nitrosoguanidine 388 resistant mutants were isolated. It is shown that the mutants isolated are probably allelic; they were phenotypically similar and no complementation was observed. The mutants were pleiotropic in the sense that although they were initially selected only for resistance to 2-deoxy-D-glucose they were found to be cross-resistant to both of the related analogues, sorbose and glucosamine. Furthermore, the mutants were unable to utilize fructose as a sole carbon source. It is demonstrated that the inability to utilize fructose results from a defect in sugar transport. The gene symbol ftr is proposed for this cistron and it is shown that though the gene is quite closely linked to its own centromere, it is unlinked to centromere markers of the six known linkage groups.

Considering a single mutant gene in a geographically subdivided finite population, it is shown that the average number of heterozygotes, due to this gene, that appear in the population before fixation or loss of this gene is equal to twice the total population number. This is invariant under the geographical structure of the population.

Chain-termination suppressors which are almost certainly amber suppressors have been isolated in Salmonella anatum by a technique involving the use of amber mutants of bacteriophage 01. The same technique could be used in any species of Salmonella (and many strains of Arizona) and analogous techniques are suggested for use in other genera of bacteria and in higher plants.

If heterozygotes for a reciprocal translocation are intercrossed, some of their viable balanced progeny result from the fusion of unbalanced gametes with complementary duplications and deficiencies of the translocated segments. Therefore, if one parent in such an intercross is homozygous for a genetic marker on one of the segments concerned, some homozygous offspring will be produced even if the other parent does not have the marker. The expected frequency of such exceptional offspring among live-born is one-sixth if the marker is on the distal (non-centromeric) side of the point of exchange and single chiasmata normally occur in each interstitial segment. Much lower frequencies are expected if the marker is on the centromeric side, since duplications and deficiencies of proximal segments occur only as a consequence of adjacent-2 disjunction, in which homologous centromeres proceed to the same pole. This is rarer than normal disjunction. Thus, by comparing the frequencies of offspring homozygous for markers on one or other side of the point of exchange, it is possible (i) to determine which marker is in the centromeric segment, (ii) to estimate the frequency of adjacent-2 disjunction, given information on the nature of meiotic configurations in the translocation concerned.

By this method, it is shown that the frequency of adjacent-2 disjunction is similar in heterozygotes for mouse translocations (T5;18)26H, T(13; ?) 70H and T(14;17)264Ca, averaging 13%. Centromeres were located at the Sd end of linkage group V (confirming previous findings), the fz end of XIII and the bg end of XIV.

Allelic recombination frequency and pattern in fungi show strong gene-to-gene variation. At least in two fungal species, Neurospora and Schizophyllum, recombination frequencies in certain chromosomal segments are genetically determined. The possibility that chromosomal proteins and/or synaptinemal complexes may play an important role in regulation of recombination frequency and pattern is discussed.

Coleoptile anthocyanin pigmentation in the hexaploid variety of wheat, Hope, is due to at least eight anthocyanins including four acylated forms. All are derivatives of either cyanidin or peonidin. Two homoeologous chromosomes, 7A and 7B, are involved in anthocyanin production. Both chromosomes carry genes that promote the synthesis of the same anthocyanins from flavonoid precursors. The roles of chromosomes 7A and 7B in anthocyanin biosynthesis and the consequences of interallelic interaction and dominance of possibly homoeologous loci are discussed.

Twenty-five population cages of D. melanogaster were set up, each containing a different wild-type second chromosome and the marker chromosome Cy. In all but one case where contamination apparently occurred, the Cy chromosome persisted in the population at high frequency, showing a selective advantage of Cy/ + heterozygotes over wild-type homozygotes. Overall, the results indicate that homozygosity of the entire second chromosome causes a depression in fitness of the order of 85%.

The structure and function of flagella are genetically determined and single gene mutants – for example, lacking in motility or of abnormal flagellar length – have previously been investigated. When such mutants are crossed with wild-type, temporary dikaryons – prozygotes – are formed with two nuclei and a common cytoplasm. The properties of the four flagella – two originally abnormal – have been observed as a function of time. In wild-type × non-motile mutant crosses, restoration of motility has been observed in a number of cases. If the dikaryons are deflagellated regeneration occurs, together with restoration of motility or of normal length to the previously abnormal pair. Complementation at the cytoplasmic level has been found in paired mutants.

It has been possible to examine the correlation between the presence of phage-like particles and R bodies by using serial sections of kappas of stock 562. No exception has been found to the rule that 562 kappa particles with R bodies also have phage-like particles; however, 3 out of 78 kappa particles with phage-like particles lacked R bodies.

The E.M.S.-induced auxotrophic mutant 1308 of Drosophila is located between 13·7 and 21·0 on chromosome 1. Survival of larvae is possible if whole RNA is provided in the diet, and this is shown to be a requirement for a source of both purines and pyrimidines. A proportion of larvae will grow on pyrimidine nucleosides alone. Tests for utilization of bases and of precursors suggest that 1308 is a double mutant, and not a single mutation preventing the synthesis of a common precursor of purines and pyrimidines.