Allozyme polymorphism and linkage disequilibrium ofAdh and α-Gpdh loci in wine cellar and field populations ofDrosophila melanogaster

Summary Over three years, theAdh and -Gpdh loci have been studied in two cellar populations ofDrosophila melanogaster and in two field populations which were each near to one of the cellars. Analyses of gene frequencies indicate that the divergence among subpopulations is greater in theAdh locus than in the -Gpdh locus. Selection for or againstAdh ^S allele acting on theIn(2L)t inversion influences of the -Gpdh alleles. This phenomenon may contribute to explain the maintenance of theAdh and -Gpdh polymorphism and of theIn(2L)t inversion.     

Age-related perseveration of the precopulatory behaviour in maleDrosophila melanogaster

Summary In response to an interruption of their courtship, males ofD. melanogaster exhibit a lasting sexual arousal (up to 30–60 min), expressed behaviourally by characteristic wing displays. A study of this effect centered on two memory mutants of different ages suggests that it can be related to an ageing-dependent perseveration, rather than to modifications in memory processing.Acknowledgments. This research was supported by an exchange grant of the Royal Society. We are grateful to Dr Linda Partridge for advice and loan of apparatus.     

Differential expression and dosage compensation of theα-amylase gene inDrosphila miranda

Summary The-amylase gene ofDrosophila miranda is located on the X²-and on the neo-Y-chromosome, both developing sex chromosomes. Crosses between strains carrying different electrophoretically distinguishable alleles of the-amylase gene were performed. Females of the F₁ offspring showed the expected heterozygosity, while the males proved to be hemizygous for this locus. Only the gene on the X²-chromosome is expressed, whereas the corresponding gene on the neo-Y-chromosome is not. Estimates of the-amylase activity in crude homogenates of male and female flies suggest strongly that the-amylase gene is dosage compensated inD. miranda. In contrast to this situation, in all otherDrosophila species the-amylase allele is autosomal and hence not dosage compensated.Acknowledgments. We would like to thank Betty C. Moore, for the kind supply ofD. miranda strains. For the help and advice in the electrophoretic separation of the-amylase variants we are indebted to Dr W. Pinsker. This work was supported by a grant from the Fonds zur Förderung der wissenschaftlichen Forschung, P5413 (Austria).     

The sensitive period for yellow phenocopy induction inDrosophila melanogaster

Summary Yellow phenocopies ofDrosophila melanogaster were produced by raising larvae on -DMT contaminated media. Using a survivorship test, the sensitive period for phenocopy induction was found to occur during the third larval instar of development, with increased survivorship at 1% -DMT compared with lower concentrations. It was also found that treatment with -DMT significantly slowed development. These findings are related to the relevant morphological and behavioral developmental pathways and to phenocopy induction.Publication No. 35 from the Evolutionary Genetics Laboratory, University of Auckland.Acknowledgments. We thank the New Zealand Entomology Society for a grant from their Anniversary Fund to R. D. Newcomb and the University Grants Committee, Research Grant No. 394.597 to D.M. Lambert.     

Heat shock proteins in three relatedDrosophila species belonging to theobscura group

The effect of heat shock on protein synthesis in three relatedDrosophila species belonging to theobscura group was analyzed on SDS-acrylamide gels. Four major heat shock proteins (hsps) were found in these species, in which synthesis reaches a maximum at 34°C. Although the higher molecular weight proteins are conserved, differences in size were found for the small hsps in these species. By means of in situ hybridization usingD. melanogaster probes for the small hsp genes, it was inferred that the small hsp genes of theobscura group species are clustered at the 27A locus in all three species.     

Mobile gene localization and viability inDrosophila melanogaster

Summary The location of the mobile element mdg-1 was determined by in situ hybridization in salivary gland chromosomes ofDrosophila melanogaster. The locations of mdg-1 are nonrandom and some hot spots exist. Moreover, the spectra of mdg-1 locations vary with the viability values of the families from which the larvae originated. This suggests that particular frequency spectra are associated with lethality resulting from inbreeding.     

Properties of the larval hemocytes ofDrosophila melanogaster

Summary Contrary to Srdi and Gloor's report, we find crystal cells (cc) in the lymph glands ofD. melanogaster larvae; the size and number of inclusions in the cc cannot be used to distinguish the 2 sibling species,D. melanogaster andD. simulans; cc in the hemocoel are not phagocytic cells; the surface properties of the lamellocytes are consistent with their derivation from plasmatocytes and not cc.Supported by grant No. CA16619 awarded by the National Cancer Institute, DHEW, USPHS.     

Hotspots of homologous recombination

Homologous recombination occurs at higher than average frequency at and near hotspots. Hotspots are special nucleotide sequences recognized by proteins that promote, directly or indirectly, a rate limiting step of recombination. This review focuses on two well-studied examples, the Chi sites of the bacteriumEscherichia coli and the M26 site of the fission yeastSchizosaccharomyces pombe. Chi, 5 G-C-T-G-G-T-G-G 3, is recognized by the RecBCD enzyme, which nicks the DNA near Chi and produces a 3-ended single-stranded DNA tail; this tail is a potent substrate for homologous pairing by RecA and single-stranded DNA binding proteins. M26, 5 A-T-G-A-C-G-T 3, is recognized by a heterodimeric protein and stimulates, by an as-yet-unknown mechanism, meiotic recombination at and near theade6 gene. Additional hotspots in bacteria, fungi, and mammals enhance recombination directly or indirectly via a variety of mechanisms. Although hotspots are widespread among organisms, the biological role of their localized enhancement of recombination remains a matter of speculation.     

Intrapopulational genetic variation in the hybridization betweenDrosophila melanogaster females andD. simulans males

Summary Intrapopulational variation on interspecific crossing ability betweenD. melanogaster andD. simulans has been measured. When themelanogaster females andsimulans males were crossed, hybridization ranged from 3 to 34%, the female component of variation being more important than the male component. This point is discussed in relation with the role played by each sex in sexual isolation.     

Ethanol metabolizing system inDrosophila melanogaster: subcellular distribution of some main enzymes

Summary The subcellular distribution of some enzymes which play a part in ethanol metabolism have been determined by differential centrifugation of homogenates of adultD. melanogaster flies of various genotypes. Aldehyde dehydrogenase, recently discovered inD. melanogaster, is present in the five genotypes studied. It has been found however to be, in vitro at least, most active in a strain lacking both alcohol dehydrogenase and aldehyde oxidase.     

Negative phototaxis inDrosophila associated with a morphological change in the compound eye

Summary The ultrastructure of the compound eyes of several photonegative selection lines and their unselected photopositive controls of five species of themelanogaster subgroup was analyzed. A qualitative phenotypic change concerning the rhabdomeres in one of the photonegative selection lines ofD. mauritiana could be detected. It was proved that this structural aberration of the rhabdomeres is caused by a parallel mutation of the mutantora (outer rhabdomeres absent) ofD. melanogaster.     

Genetic load and effective size of natural populations ofDrosophila melanogaster in Korea

Summary The effect of 750 second chromosomes ofDrosophila melanogaster on viability was studied. 19.3% of them proved letal or semilethal (=drastics) in homozygous condition. Compared to data obtained in previous years at the same sampling site, a significant frequency decrease of drastics during the past decade could be observed. The dynamic processes taking place in the Korean wild populations ofD. melanogaster are discussed.Acknowledgment. This work was supported by a research grant from the Korean Science and Engineering Foundation.     

Acetaldehyde metabolism inDrosophila melanogaster

Summary A quantitative study on in vitro acetaldehyde degradation in homogenates fromDrosophila melanogaster files shows that aldehyde oxidase plays the major part in acetaldehyde detoxification. However, in a strain, celed AO null, because itsAldox locus produces no aldehyde-oxidase, acetaldehyde is also degradated by a still unknown mechanism. Alcoholdehydrogenase which is responsible for the dehydrogenation of ethanol in acetaldehyde, appears to catalyze the reversed reactions as wel, regenerating ethanol fromacetaldehyde.This work was supported in part by a grant from the FNRS of Belgium.     

Single amino acid substitutions insn-glycerol-3-phosphate dehydrogenase allozymes fromDrosophila virilis

Summary The amino acid sequence was compared among the three allelic variants (allozymes) ofsn-glycerol-3-phosphate dehydrogenase inD. virilis, which are detected by one-dimensional electrophoresis. The GPDH^f variant was different from the GPDH^m by only one substitution of 68-lysine for asparagine; GPDH^s differed from GPDH^m by substitution of 127-glycine for arginine. No electrophoretically silent substitutions were found in a total of 352 amino acid residues.     

Can we predict the mating pattern ofDrosophila females from the sperm length distribution in males?

Summary In order to test the validity of the prediction of the mating pattern of females from the sperm length distribution in males, three species ofDrosophila were analysed. Males in the three species are equally polygynous but females differ in the level of polyandry. A low recurrence polyandry is observed in the sperm dimorphic speciesD. affinis while a high recurrence polyandry is observed in the sperm monomorphic speciesD. latifasciaeformis andD. littoralis. These results are consistent with the hypothesis proposed previously that sperm dimorphism in males can only be maintained by a selective alternative in females (i.e. facultative female polygamy), whereas a stricter mating system (e.g., obligatory polyandry) should only result in sperm monomorphism irrespective of the absolute value of sperm length.     

Differences in chromosome A arrangement betweenDrosophila madeirensis andDrosophila subobscura

Summary The proximal half of the A (=X) chromosome ofD. madeirensis has a gene arrangement very similar to the A1 or A6 inversions found inD. subobscura. Polytene chromosome analysis of hybrids betweenD. madeirensis and strains ofD. subobscura homozygous for such inversions shows, however thatD. madeirensis has a gene arrangement different from any known forD. subobscura. These results provide evidence for a greater differentiation of the X chromosome in these species than has previously been described; it seems that the X chromosome is the only one that has undergone structural variation during the speciation process.     

The in vivo role of α-mannosidase IIx and its role in processing of <Emphasis Type="Italic">N</Emphasis>-glycans in spermatogenesis

The surfaces of mammalian cells are covered by a variety of carbohydrates linked to proteins and lipids. N-glycans are commonly found carbohydrates in plasma membrane proteins. The structure and biosynthetic pathway of N-glycans have been analyzed extensively. However, functional analysis of cell surface N-glycans is just under way with recent studies of targeted disruption of genes involved in N-glycan synthesis. This review briefly introduces the potential role of processing -mannosidases in N-glycan biosynthesis and recent findings derived from the -mannosidase IIx (MX) gene knockout mouse, which shows male infertility. Thus, the MX gene knockout experiment unveiled a novel function of specific N-glycan, which is N-acetylglucosamine-terminated and fucosylated triantennary structure, in the adhesion between germ cells and Sertoli cells. Analysis of the MX gene knockout mouse is a good example of a multidisciplinary approach leading to a novel discovery in the emerging field of glycobiology.Received 29 November 2002; received after revision 30 December 2002; accepted 20 January 2003     

Genetic variation at the alcohol dehydrogenase locus inDrosophila melanogaster: A third ubiquitous allele

Summary A 3rd allele at theAdh locus,Adh ^FCh.D., has been found at polymorphic frequencies in natural populations ofD. melanogaster. The ADH-FChD enzyme has properties distinct from those of the 2 more common forms of ADH. TheAdh polymorphism should now be analyzed as a triallelic system.     

Dominance for enzyme activity inDrosophila melanogaster

Summary A regulatory element tightly linked to theGpdh locus inDrosophila melanogaster has been isolated from a natural population. Flies homozygous for second chromosomes bearing the element,H31, have half the GPDH activity of normal homozygotes. Heterozygotes betweenH31 andF orS alleles exhibit dominance in GPDH activity. Heterozygotes betweenH31, F orS andDf(2L) GdhA have half the diploid level. The contribution of theS allele to the activity inS/H31 heterozygotes is more than four times that ofH31. The regulatory element distinguishingH31 is tightly linked to theGpdh ⁺ locus.     

A human homolog of the yeast gene encoding tRNA 2′-phosphotransferase: cloning,characterization and complementation analysis

The Saccharomyces cerevisiae TPT1 gene plays a role in removing the 2-phosphate from ligated tRNA during the maturation of pre-tRNA. Here we reported the cloning and characterization of the human TRPT1 gene as a homolog of yeast TPT1. The TRPT1 gene is located at human chromosome 11q13 and encodes a polypeptide of 253 amino acids. BLAST searches with its amino acid sequence revealed the ubiquitous occurrence of TRPT1 homologs and their functional relationships with the presence of the DUF60/KptA domain. Northern analysis demonstrated that the gene is primarily expressed in heart and skeletal muscle, with lower or undetectable levels in other tissues studied. A plasmid-shuffling experiment showed that the human TRPT1 gene could complement the tpt1 mutation in S. cerevisiaeReceived 19 March 2003; received after revision 25 April 2003; accepted 22 May 2003