The present investigation primarily deals with the inheritance of a pigmeat quality trait, the Napole technological yield (RTN), a measure of cooked weight to fresh weight. This trait as well as lean percentage at 100 kg liveweight and fattening length from 20 to 100 kg liveweight were recorded on 3459 offspring from 67 sires and 433 dams, and 3052 offspring from 64 sires and 405 dams in Penshire (P66) and Pen Ar Lan (P77) composite lines respectively. The hypothesis of a major 2-allele locus contributing to RTN was tested by use of a segregation analysis method. Highly significant likelihood ratios (mixed vs. polygenic transmission models) lead us to conclude that a major gene RN− exerting an unfavourable effect on RTN is segregating in both lines. Maximum likelihood estimates of the parameters under the hypothesis of mixed (monogenic + polygenic) inheritance show that the difference between the means of the 2 homozygotes amounts to about 3 phenotypic standard deviations of the trait, whereas the complete dominance of RN− cannot be rejected. The frequency of RN− is about 0·6 in both lines. These results are discussed in connection with the previously reported ‘Hampshire effect’ on pigmeat quality, as the Hampshire breed is a common component of the foundation stock of the 2 composite lines under study.

Oocytes from (C3H/HeH × 101/H)F1 and Rb(16.17)7Bnr homozygous females were exposed to a range of doses of nocodazole in vitro. The spindle poison caused a dose dependent increase in metaphase I (MI) arrest and hyperploidy. A concentration of 0·03 μg/ml was found to induce a maximum hyperploid frequency of 3·1% and 11·6% respectively without a high level of MI arrest. Between 0·03 and 0·05 μg/ml MI arrest increased substantially and reached a frequency of approximately 90%. In a further experiment oocytes from Rb7 homozygous, heterozygous and 3H1 females were exposed to 0·03 μg/ml nocodazole 4, 6 or 8 h after the onset of maturation. The phase at which the spindle was inhibited resulted in a specific pattern of nondisjunction which in turn was dependent on whether the female carried an Rb metacentric. 3H1 oocytes gave a normally distributed pattern of increase in aneuploid frequency (over the spontaneous value) centering around a 6 h application. This was thought to be due to the interaction of chromosomes with the microtubules of the spindle during attachment and/or alignment. In contrast both Rb homozygotes and heterozygotes gave the same biphasic response, with a high frequency of aneuploidy in the oocytes when nocodazole was applied 4 and 8 h after the onset of maturation. In Rb homozygotes we demonstrated that the Rb bivalent underwent nondisjunction more frequently than the average acrocentric, when nocodazole was administered early. It can be assumed that the Rb trivalent in Rb heterozygotes showed a similar response. This early Rb specific effect, in combination with a delayed-version of the acrocentric effect found in the 3H1 mice was thought to generate the biphasic pattern. We discuss the implications of (a) the different meiotic behaviours of metacentrics and acrocentrics and (b) the meiotic delay in Rb mice.

In haploid strains of Aspergillus nidulans, asci arise from croziers. The two nuclei of the young ascus (the penultimate cell of the crozier) fuse, and the zygote nucleus immediately undergoes meiosis. At diakinesis and first metaphase eight bivalents are seen: three large (one, Chromosome 2, with a satellite), two medium sized (Chromosomes 4 and 5), two small (Chromosomes 6 and 7) and one very small (Chromosome 8). The perithecia of haploid strains are packed with asci and have very few sterile hyphae.

Diploid strains (heterozygotes made by Roper's technique) are very different from haploids in that the perithecia contain many sterile hyphae with little cytoplasm and coiled hyphae with dense cytoplasm made up mainly of uninucleate cells, and there are few asci in a perithecium. Croziers are absent: some of the cells of the coiled hyphae become asci. At diakinesis and first metaphase, the same chromosome configurations are seen as in a cross between the haploid strains from which the diploid was synthesized; the chromosomes are bivalents. The young ascus thus has a single (diploid) nucleus which undergoes meiosis, and asci develop apogamously. No evidence of nuclear fusion in the young ascus and of a tetraploid meiosis was obtained. Cultures from ascopores isolated by micro-manipulation from perithecia of diploids were all haploid. Meiosis appears to proceed normally to first metaphase, but typical later stages, and asci with spores, are rarely seen. First anaphase frequently fails to occur, and the chromosomes clump together.

In the strain ad2 y, obtained from a normal strain by X-irradiation, nine bivalents are present, one a very small fragment. In crosses between ad2 y and a normal strain, and in a diploid made from them, the fragment pairs with Chromosome 6. Asci in the cross between ad2 y and a normal haploid are highly irregular, often with less than the usual eight spores.

Destruction by laser microbeam of oral and ventral cirral primordia for the future opisthe of 1/2 of a pre-fission doublet results in the permanent loss of ability to form oral and ventral cirral primordia on the irradiated half. This observation provides further evidence for the postulated ‘determinative region’ present on each ventral surface of these organisms. The opisthe of the irradiated doublet retains both original rows of marginal cirri, which are located mid-dorsally with respect to the remaining ventral surface. These two rows of marginal cirri are reproduced faithfully in all future opisthes, but are lost in most proter lines. The pattern of loss in proters involves migration of the extra rows of marginal cirri to the cell's right margin followed by aberrant morphogenesis and subsequent resorption. These results show that the reproduction of marginal cirri is at least partially dependent upon the presence of marginal cirri and their inherent structural characteristics as well as upon their position on the cell surface.

Segregation of the prophage of bacteriophage 90 has been observed in reciprocal crosses between lysogenic and non-lysogenic parents of Pseudomonas aeruginosa strain PAO. Linkage of the prophage was shown to three genes determining histidine biosynthesis in that region of the chromosome 7–13 min from the site on the chromosome at which the sex factor FP2 promotes chromosome mobilization.

An estimator is proposed for the parameter C = 4Nc. where N is the population size and c is the recombination rate. The estimator is appropriate for use with sequence or restriction site data from random samples from within populations. Properties of the estimator are investigated for an infinite-sites neutral model using Monte Carlo simulations. The median and mode of the distribution of the estimator are close to the true value for all parameter values examined, but large data sets are required to obtain reliable estimates.

X chromosome inactivation (XCI) has been assumed to be complete in all cells of female mouse embryos at about 6 d post coitum (dpc). However, a recent study on β-galactosidase expression of an X-linked lacZ transgene suggests that XCI is probably not complete several days after this time in some lineages. To help resolve this issue, we analysed XCI in embryos which carry the T(X;16)16H (Searle's) translocation and are heterozygous at the X-linked Hprt and Pgk-1 genes. The quantitative RT-PCR single nucleotide primer extension (SNuPE) assay was used to measure Hprt and Pgk-1 allele-specific transcripts in embryos 9·5 dpc. No transcripts from the normal X chromosome were found in any of the tissues tested, indicating that inactivation was complete for these endogenous genes.

IIIRa is a genetic modifier of Segregation Distortion (SD) in Drosophila melanogaster, which was discovered in the same natural population from Ranna (Sicily) that carried SDRa. It is located at 49·7 ± 0·8 on chromosome III. IIIRa was found to have a dominant effect on segregation distortion which varied with the origin of the SD chromosome tested. Thus it enhanced the level of distortion caused by 14 SD chromosomes from seven natural populations in Southern Italy and Sicily, but decreased the level of distortion caused by SDR−1, a chromosome from a natural population near Rome. Moreover, IIIRa determined or enhanced the distorting effect of SDRa in males heterozygous for SDRa and various SD+ wild chromosomes differently sensitive to SDRa. The frequency of chromosomes having an effect like IIIRa chromosome was very high (around 70%) in samples from two natural populations of Southern Italy tested-those of Ranna and Corato. No effects of IIIRa other than its ability to modify SD have been detected.

Non-germinating gibberellin (GA) responsive mutants are a powerful tool to study genetic fine structure in higher plants. Nine alleles (EMS-and fast neutron-induced) of the ga-1 locus of Arabidopsis thaliana were tested in a complete half-diallel. No wild type ‘recombinants’ were found in the selfed progeny of 9 homoallelic combinations (in total 3 × 105 plants); in the progenies from the 36 selfed hetero allelics the wild type frequency ranged from zero to 6·6 × 10−4. These frequencies allowed the construction of an internally consistent map for five different sites representing eight alleles. The ninth allele covered three sites and thus behaved like an intragenic deletion. The estimate of the total genetic length of the ga-1 locus was 0·07 cM. The order of the sites was also clearly reflected by the association with proximal outside markers. On the assumption that wild type gametes predominantly arise from reciprocal events, it was shown that a cross-over within the ga-1 locus leads to positive interference in the adjacent region.

The results are discussed with respect to the mutagen used, the frequencies found in other plant and Drosophila genes, and the possible occurrence of gene conversion.

Over twenty distinct families of long terminal direct repeat (LTR)-containing retrotransposons have been identified in Drosophila melanogaster. While there have been extensive analyses of retrotransposon transcription in cultured cells, there have been few studies of the spatial expression of retrotransposons during normal development. Here we report a detailed analysis of the spatial expression patterns of fifteen families of retrotransposons during Drosophila melanogaster embryogenesis (17.6, 297, 412, 1731, 3S18, blood, copia, gypsy, HMS Beagle, Kermit/flea, mdg1, mdg3, opus, roo/B104 and springer). In each case, analyses were carried out in from two to four wild-type strains. Since the chromosomal insertion sites of any particular family of retrotransposons vary widely among wild-type strains, a spatial expression pattern that is conserved among strains is likely to have been generated through interaction of host transcription factors with cis-regulatory elements resident in the retrotransposons themselves. All fifteen families of retrotransposons showed conserved patterns of spatially and temporally regulated expression during embryogenesis. These results suggest that all families of retrotransposons carry cis-acting elements that control their spatial and temporal expression patterns. Thus, transposition of a retrotransposon into or near a particular host gene-possibly followed by an excision event leaving behind the retrotransposon's cis-regulatory sequences-might impose novel developmental control on such a host gene. Such a mechanism would serve to confer evolutionarily significant alterations in the spatio-temporal control of gene expression.

Acridine orange does not interfere with the distribution of the F-particles among the daughter cells but inhibits the multiplication of the episome.

In growing cells the generation time of the episome in the presence of acridine orange is longer than the generation time of the cell.

This lowers the number of episomes per cell to less than two copies at cell division.

F-particles rapidly multiply after transfer until a relatively small fixed number (3–4) is reached.

Amongst a collection of temperature sensitive (TS) mutants of Escherichia coli K-12, some have been found which can grow at the restrictive temperature (42 °C) if the osmotic pressure of the medium is raised by the addition of sodium chloride (1%) or sucrose (12·5%). These mutants are described as temperature sensitive osmotic remedial (TSOR) mutants. At the restrictive temperature they are not osmotically fragile, but do display decreased resistance to inhibitory agents such as deoxycholate, actino-mycin D and acridine orange; they also show release of the periplasmic enzyme ribonuclease. These results indicate a change in the cell's outer permeability barrier. The genes affected in six of the mutants have been located on the E. coli linkage map. The mutations, which occur at loci not previously described, have been named envM–envT to indicate their effect on the cell envelope.

A spontaneous autosomal mutation in C57BL/Tb mice, provisionally called reduced pigmentation, symbol rp, has pronounced effects on three kidney lysosomal glycosidase activities. Homozygous rprp mice have significantly higher activities of β-galactosidase, β-glucuronidase and N-acetyl-β-hexosaminidase than their heterozygous litter-mates. Homozygotes have light ears and tails, diluted fur and dark eyes. The mutation is not allelic to any known to affect lysosomal functions, or to a number of pigmentation variants with similar phenotypic effects. The locus is on chromosome 7.

A new locus for choline-requirement has been identified in Aspergillus nidulans and designated choC3. It has been located to linkage group VIII at a position 31·9 ± 2·2 map units to the left of the sD locus.

It is proposed that this locus codes either for the enzyme that catalyses the transmethylation of phosphatidyl monomethylaminoethanol to phosphatidyl dimethylaminoethanol or for a molecule essential for the synthesis or function of this enzyme.

Tabby males were irradiated with 500 r and mated to Bn Mobr♀♀. Daughters conceived during the first 3 weeks after irradiation were tested for the presence of sex-linked recessive mutations in their progeny, each daughter representing one irradiated gamete. One visible, but no lethal, was found in the Bn–Mobr segment among 154 tested gametes; one gamete was proved free of lethals or visibles in the Bn–Ta segment, and 21 gametes in the Ta–Mobr segment. Among the whole 176 tested gametes there was no indication of a lethal in the adjoining segments.

Hitch-hiking of dispersed mobile elements serving as molecular markers was used as a new tool for mapping quantitative trait loci in Drosophila melanogaster. Two Drosophila strains with high fitness (HA) were backcrossed repeatedly to a closely related strain with low fitness (LA) to initiate experimental populations with expected HA gene frequencies of 1/32. The frequencies of 19 insertion sites of the retrotransposons mdg1 and copia were analyzed after 11 to 17 generations. Frequencies of sites from the HA line increased substantially in the pericentromeric region, indicating that one or more loci responsible for the fitness difference between the strains were located there. A maximum likelihood (ML) procedure was applied to estimate selection coefficients associated with the markers, and this indicated a broad, strongly selected region of the chromosome. At least one additional locus was localized in the middle of the 2L arm. Possible applications of this method are discussed.