TEMPERATURE-SENSITIVE MUTATIONS IN DROSOPHILA MELANOGASTER.: II. FREQUENCY AMONG SECOND CHROMOSOME RECESSIVE LETHALS INDUCED BY ETHYL METHANESULFONATE

1968 ◽  
Vol 10 (2) ◽  
pp. 412-420 ◽  
Author(s):  
David Baillie ◽  
David T. Suzuki ◽  
Mary Tarasoff
Keyword(s):  
Drosophila Melanogaster ◽  
Temperature Sensitivity ◽  
Ethyl Methanesulfonate ◽  
Temperature Sensitive ◽  
Chromosome 2 ◽  
Genetic Studies ◽  
Recessive Lethal

Recessive lethal and semilethal mutations induced in chromosome 2 by ethyl methanesulfonate were screened for temperature-sensitivity. Mutants which survive at 17 °C but die at 29° were recovered. At 0.005M EMS, 37.5% of the treated chromosomes were found to be lethal or semilethal from which it is estimated that 10.9% of all EMS-induced lethals are ts. This class of conditional lethals promises to be a useful tool in genetic studies.

scholarly journals TEMPERATURE-SENSITIVE MUTATIONS IN DROSOPHILA MELANOGASTER. IX. DOMINANT COLD-SENSITIVE LETHALS ON THE AUTOSOMES

Genetics ◽  
1972 ◽  
Vol 70 (1) ◽  
pp. 75-86
Author(s):  
Raja Rosenbluth ◽  
Dean Ezell ◽  
David T Suzuki
Keyword(s):  
Drosophila Melanogaster ◽  
Maternal Effect ◽  
Ethyl Methanesulfonate ◽  
Temperature Sensitive ◽  
Chromosome 2 ◽  
Prolonged Incubation ◽  
Larval Instars ◽  
Lethal Mutations ◽  
Cold Sensitive

ABSTRACT Ethyl methanesulfonate-treated autosomes were screened for the presence of dominant cold-sensitive (DCS) lethal mutations in Drosophila melanogaster. None was found among 6,552 treated and 168 untreated third chromosomes. Twenty-three DCS-L chromosomes which caused death at 17°C but survived at 22°C and 29°C were recovered from 5,046 mutagenized chromosome 2's.—The DCS-L mutations all mapped around dp and appeared to be functionally allelic. Lethality of heterozygotes for most of the DCS-L's occurred over a prolonged interval from the embryonic through the larval instars. Prolonged incubation at 17°C did not demonstrate any maternal effect on zygotic survival.

A CYTOGENETIC ANALYSIS OF THE CHROMOSOMAL REGION SURROUNDING THE α-GLYCEROPHOSPHATE DEHYDROGENASE LOCUS OF DROSOPHILA MELANOGASTER

Genetics ◽  
1983 ◽  
Vol 105 (2) ◽  
pp. 371-386
Author(s):  
Michael A Kotarski ◽  
Sally Pickert ◽  
Ross J MacIntyre
Keyword(s):  
Drosophila Melanogaster ◽  
Polytene Chromosome ◽  
Cytogenetic Analysis ◽  
Chromosomal Region ◽  
Chromosome Band ◽  
Recombination Analysis ◽  
Chromosome 2 ◽  
Recessive Lethal ◽  
Lethal Mutations ◽  
Glycerophosphate Dehydrogenase

ABSTRACT The chromosomal region surrounding the structural gene for α-glycerophosphate dehydrogenase (αGpdh, 2-20.5) of Drosophila melanogaster has been studied in detail. Forty-three EMS-induced recessive lethal mutations and five previously identified visible mutations have been localized within the 25A-27D region of chromosome 2 by deficiency mapping and in some cases by a recombination analysis. The 43 lethal mutations specify 17 lethal loci. ?Gpdh has been localized to a single polytene chromosome band, 25F5, and there apparently are no lethals that map to the αGpdh locus.

scholarly journals TEMPERATURE-SENSITIVE MUTATIONS IN DROSOPHILA MELANOGASTER. XVII. HEAT- AND COLD-SENSITIVE LETHALS ON CHROMOSOME 3

Genetics ◽  
1973 ◽  
Vol 74 (3) ◽  
pp. 509-520
Author(s):  
S Elaine Tasaka ◽  
David T Suzuki
Keyword(s):  
Drosophila Melanogaster ◽  
Ethyl Methanesulfonate ◽  
Cold Sensitivity ◽  
Chromosome 3 ◽  
Temperature Sensitive ◽  
Single Mutation ◽  
Physical Length ◽  
Lethal Mutations ◽  
Genetic Length ◽  
Cold Sensitive

ABSTRACT Ethyl methanesulfonate-treated third chromosome of Drosophila melanogaster were tested for the presence of dominant and recessive temperature-sensitive lethal mutations at 17°, 22° and 29°C. Out of 1,176 chromosomes tested, no dominant ts lethals, 21 heat-sensitive, 22 cold-sensitive and 10 heat-cold-sensitive lethals were recovered. Heat-cold sensitivity was produced by a single mutation in all cases. Sixty-two percent of the ts lethals were fertile as homozygotes in both sexes. Surprisingly, 88% of the ts lethals mapped between st and Sb, a region straddling the centromere and estimated to comprise 12.9% of the genetic length and 55% of the physical length of chromosome 3. All but one of the heat- and cold-sensitive lethals complemented with each other at their respective restrictive temperatures.

scholarly journals Decreased Temperature Sensitivity of Vestigial Gene Expression in Temperate Populations of Drosophila melanogaster

Genes ◽  
2019 ◽  
Vol 10 (7) ◽  
pp. 498
Author(s):  
Voigt ◽  
Erpf ◽  
Stephan
Keyword(s):  
Gene Expression ◽  
Drosophila Melanogaster ◽  
Temperature Sensitivity ◽  
Natural Populations ◽  
Limiting Factor ◽  
Temperature Sensitive ◽  
Thermal Environments ◽  
Wide Range ◽  
Key Factor ◽  
Temperate Climates

Drosophila melanogaster recently spread from its tropical origin in Africa and became a cosmopolitan species that has adapted to a wide range of different thermal environments, including temperate climates. An important limiting factor of temperate climates has probably been their low and varying temperatures. The transcriptional output of genes can vary across temperatures, which might have been detrimental while settling in temperate environments. The reduction of temperature-sensitive expression of functionally important genes to ensure consistent levels of gene expression might have been relevant while adapting to such environments. In this study, we focus on the gene vestigial (vg) whose product is a key factor in wing development. We provide evidence that temperature-sensitivity of vg has been buffered in populations from temperate climates. We investigated temperature-sensitivity of vg gene expression in six natural populations, including four temperate populations (three from Europe and one from high-altitude Africa), and two tropical populations from the ancestral species range. All temperate populations exhibited a lower degree of temperature-induced expression plasticity than the tropical populations.

INVITATION PAPER: BEHAVIOR IN DROSOPHILA MELANOGASTER A GENETICIST'S VIEW

1974 ◽  
Vol 16 (4) ◽  
pp. 713-735 ◽  
Author(s):  
David T. Suzuki
Keyword(s):  
Drosophila Melanogaster ◽  
Sodium Channel ◽  
Temperature Sensitivity ◽  
Temperature Sensitive ◽  
Neuronal System ◽  
Neurological Development ◽  
Temperature Changes ◽  
Early Embryos ◽  
Induced Changes

In screening Drosophila melanogaster for mutations which cause paralysis at 29cC and recovery of mobility at 22cC, 11 temperature-sensitive (ts) mutants were detected among 1.35 × 106 flies screened. These mutations fell into 3 loci, paralytic (parats), shibire (shits) and stoned (stnts). All three loci affect neurological development. The best explanation for parats appears to be an effect on the inhibitory neuronal system. The shi alleles affect an array of developmental events from early embryos to adults. The pattern of heat-induced changes in shits1 electroretinograms (ERG) is consistent with a ts membranal defect. This is supported by a ts resistance of shits flies to tetrodotoxin which specifically blocks the sodium channel of nerves.The final locus, stn, causes sensitivity to the trauma of temperature changes. A jump response observed when a light is turned off is related to a large "offtransient" in ERGs which is correlated with a simultaneous muscle spike. The property of temperature-sensitivity allows greater analytic powers in the study of neurological mutants.

scholarly journals Cytogenetic analysis of chromosome region 73AD of Drosophila melanogaster.

Genetics ◽  
1990 ◽  
Vol 125 (4) ◽  
pp. 783-793
Author(s):  
J M Belote ◽  
F M Hoffmann ◽  
M McKeown ◽  
R L Chorsky ◽  
B S Baker
Keyword(s):  
Drosophila Melanogaster ◽  
Mutational Analysis ◽  
Chromosome Region ◽  
Temperature Sensitive ◽  
Recessive Lethal ◽  
Male And Female ◽  
Complementation Groups ◽  
Molecular Maps ◽  
Dominant Temperature Sensitive ◽  
Dark Body

Abstract The 73AD salivary chromosome region of Drosophila melanogaster was subjected to mutational analysis in order to (1) generate a collection of chromosome breakpoints that would allow a correlation between the genetic, cytological and molecular maps of the region and (2) define the number and gross organization of complementation groups within this interval. Eighteen complementation groups were defined and mapped to the 73A2-73B7 region, which is comprised of 17 polytene bands. These complementation groups include the previously known scarlet (st), transformer (tra) and Dominant temperature-sensitive lethal-5 (DTS-5) genes, as well as 13 new recessive lethal complementation groups and one male and female sterile locus. One of the newly identified lethal complementation groups corresponds to the molecularly identified abl locus, and another gene is defined by mutant alleles that exhibit an interaction with the abl mutants. We also recovered several mutations in the 73C1-D1.2 interval, representing two lethal complementation groups, one new visible mutant, plucked (plk), and a previously known visible, dark body (db). There is no evidence of a complex of sex determination genes in the region near tra.

scholarly journals A genetic analysis of hermaphrodite, a pleiotropic sex determination gene in Drosophila melanogaster.

Genetics ◽  
1994 ◽  
Vol 136 (1) ◽  
pp. 195-207
Author(s):  
M A Pultz ◽  
G S Carson ◽  
B S Baker
Keyword(s):  
Drosophila Melanogaster ◽  
Genetic Analysis ◽  
Sex Determination ◽  
Temperature Sensitivity ◽  
Sexual Differentiation ◽  
Regulatory Genes ◽  
Temperature Sensitive ◽  
Partial Loss ◽  
Female Progeny ◽  
Regulatory Cascade

Abstract Sex determination in Drosophila is controlled by a cascade of regulatory genes. Here we describe hermaphrodite (her), a new component of this regulatory cascade with pleiotropic zygotic and maternal functions. Zygotically, her+ function is required for female sexual differentiation: when zygotic her+ function is lacking, females are transformed to intersexes. Zygotic her+ function may also play a role in male sexual differentiation. Maternally, her+ function is needed to ensure the viability of female progeny: a partial loss of her+ function preferentially kills daughters. In addition, her has both zygotic and maternal functions required for viability in both sexes. Temperature sensitivity prevails for all known her alleles and for all of the her phenotypes described above, suggesting that her may participate in an intrinsically temperature-sensitive process. This analysis of four her alleles also indicates that the zygotic and maternal components of of her function are differentially mutable. We have localized her cytologically to 36A3-36A11.

scholarly journals HOMOEOSIS IN DROSOPHILA: A NEW ENHANCER OF POLYCOMB AND RELATED HOMOEOTIC MUTATIONS

Genetics ◽  
1983 ◽  
Vol 105 (2) ◽  
pp. 357-370
Author(s):  
Takashi Sato ◽  
Michael A Russell ◽  
R E Denell
Keyword(s):  
Drosophila Melanogaster ◽  
Gene Product ◽  
Point Mutations ◽  
Lethal Mutation ◽  
Chromosome 2 ◽  
Gene Complex ◽  
Recessive Lethal ◽  
Recessive Lethal Mutation ◽  
Sex Comb

ABSTRACT A new recessive lethal mutation in Drosophila melanogaster, Enhancer of Polycomb [E(Pc)], and chromosomal deficiencies lacking this locus act as dominant enhancers of the Polycomb mutant syndrome in adults. Thus, although E(Pc)/+ flies are phenotypically normal, this locus is haplo-abnormal with respect to its effect on the Polycomb phenotype. Recombinational and deficiency mapping localize the E(Pc) locus on chromosome 2 proximally and very closely linked (∼0.1 map unit) to the engrailed gene. E(Pc) enhances the expression of all Polycomb point mutations examined including that of a deficiency, indicating that this interaction does not depend on the presence of an altered Polycomb gene product. In several respects the mutations extra sex comb, lethal(4)29, and Polycomblike resemble those at the Polycomb locus. In the presence of E(Pc), recessive alleles of extra sex comb and lethal(4)29 are rendered slightly pseudodominant, and the homoeotic effects of Polycomblike heterozygotes are also enhanced. However, E(Pc) does not affect the expression of dominant mutations within the Bithorax gene complex (Cbx) or Antennapedia gene complex (AntpNs, Antp  73b, Antpscx, AntpEfW15, ScrMsc) which give homoeotic transformations resembling those of the Polycomb syndrome. Available evidence from the study of adult phenotypes suggests that mutations at E(Pc) do not result in homoeotic changes directly but instead modify the expression of a specific set of functionally related homoeotic variants.

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