scholarly journals Dunce mutants of Drosophila melanogaster: mutants defective in the cyclic AMP phosphodiesterase enzyme system.

1981 ◽  
Vol 90 (1) ◽  
pp. 101-107 ◽  
Author(s):  
R L Davis ◽  
J A Kiger
Keyword(s):  
Enzyme Activity ◽  
Drosophila Melanogaster ◽  
Cyclic Amp ◽  
Enzyme System ◽  
Residual Enzyme Activity ◽  
Wild Type ◽  
Camp Content ◽  
Mutant Strains ◽  
Normal Enzyme ◽  
Type Strains

The cyclic AMP and cyclic GMP phosphodiesterase activities present in flies of six mutant strains of the dunce gene and in the parent wild-type strains are characterized. All of the mutants exhibit aberrant cyclic AMP metabolism. The mutant strains dunceM14, dunceM11, and dunceML appear to be amorphic, because they completely lack the cAMP-specific phosphodiesterase normally present in adult flies. These strains exhibit extremely high levels of cAMP. The mutant strains dunce1, dunce2, and dunceCK are hypomorphic and exhibit reduced levels of the cAMP-specific phosphodiesterase. These strains exhibit less marked increases in cAMP content compared with the three amorphic strains. The dunce2 strain possesses a residual enzyme activity that exhibits anomalous kinetics compared with those of the normal enzyme. The possibility that the dunce locus is the structural gene for the cAMP-specific phosphodiesterase is discussed.

scholarly journals The hobo Transposable Element Excises and Has Related Elements in Tephritid Species

Genetics ◽  
1996 ◽  
Vol 143 (3) ◽  
pp. 1339-1347
Author(s):  
Alfred M Handler ◽  
Sheilachu P Gomez
Keyword(s):  
Drosophila Melanogaster ◽  
Ceratitis Capitata ◽  
Bactrocera Dorsalis ◽  
Parsimony Analysis ◽  
Wild Type ◽  
Anastrepha Suspensa ◽  
Tephritid Species ◽  
Mutant Strains ◽  
Almost All ◽  
Horizontal Transfers

Abstract Function of the Drosophila melanogaster hobo transposon in tephritid species was tested in transient embryonic excision assays. Wild-type and mutant strains of Anastrepha suspensa, Bactrocera dorsalis, B. cucurbitae, Ceratitis capitata, and Toxotrypana curvicauda all supported hobo excision or deletion both in the presence and absence of co-injected hobo transposase, indicating a permissive state for hobo mobility and the existence of endogenous systems capable of mobilizing hobo. In several strains hobo helper reduced excision. Excision depended on hobo sequences in the indicator plasmid, though almost all excisions were imprecise and the mobilizing systems appear mechanistically different from hobo. hobe-related sequences were identified in all species except T. curvicauda. Parsimony analysis yielded a subgroup including the B. cucurbitae and C. capitata sequences along with hobo and Hermes, and a separate, more divergent subgroup including the A. suspensa and B. dorsalis sequences. All of the sequences exist as multiple genomic elements, and a deleted form of the B. cucurbitae element exists in B. dorsalis. The hobo-related sequences are probably members of the hAT transposon family with some evolving from distant ancestor elements, while others may have originated from more recent horizontal transfers.

Calreticulin Mediates Anesthetic Sensitivity in Drosophila melanogaster 

2003 ◽  
Vol 99 (4) ◽  
pp. 867-875 ◽  
Author(s):  
Sumiko Gamo ◽  
Junya Tomida ◽  
Katsuyuki Dodo ◽  
Dai Keyakidani ◽  
Hitoshi Matakatsu ◽  
...  
Keyword(s):  
Drosophila Melanogaster ◽  
Double Mutant ◽  
Developmental Stages ◽  
Northern Blotting ◽  
General Anesthetics ◽  
Wild Type ◽  
Mutant Strains ◽  
Low Expression

Background Various species, e.g., Caenorhabditis elegans, Drosophila melanogaster, and mice, have been used to explore the mechanisms of action of general anesthetics in vivo. The authors isolated a Drosophila mutant, ethas311, that was hypersensitive to diethylether and characterized the calreticulin (crc) gene as a candidate of altered anesthetic sensitivity. Methods Molecular analysis of crc included cloning and sequencing of the cDNA, Northern blotting, and in situ hybridization to accomplish the function of the gene and its mutation. For anesthetic phenotype assay, the 50% anesthetizing concentrations were determined for ethas311, revertants, and double-mutant strains (wild-type crc transgene plus ethas311). Results Expression of the crc 1.4-kb transcript was lower in the mutant ethas311 than in the wild type at all developmental stages. The highest expression at 19 h after pupation was observed in the brain of the wild type but was still low in the mutant at that stage. The mutant showed resistance to isoflurane as well as hypersensitivity to diethylether, whereas it showed the wild phenotype to halothane. Both mutant phenotypes were restored to the wild type in the revertants and double-mutant strains. Conclusion ethas311 is a mutation of low expression of the Drosophila calreticulin gene. The authors demonstrated that hypersensitivity to diethylether and resistance to isoflurane are associated with low expression of the gene. In Drosophila, calreticulin seems to mediate these anesthetic sensitivities, and it is a possible target for diethylether and isoflurane, although the predicted anesthetic targets based on many studies in vitro and in vivo are the membrane proteins, such as ion channels and receptors.

scholarly journals The Entner-Doudoroff Pathway Has Little Effect on Helicobacter pylori Colonization of Mice

2003 ◽  
Vol 71 (5) ◽  
pp. 2920-2923 ◽  
Author(s):  
Amy E. Wanken ◽  
Tyrrell Conway ◽  
Kathryn A. Eaton
Keyword(s):  
Helicobacter Pylori ◽  
Wild Type ◽  
Mutant Strains ◽  
H Pylori ◽  
Type Strains

ABSTRACT Helicobacter pylori mutants deficient in 6-phosphogluconate dehydratase (6PGD) were constructed. Colonization densities were lower and minimum infectious doses were higher for mutant strains than for wild-type strains. In spite of better colonization, however, wild-type strains did not displace the mutant in cocolonization experiments. Loss of 6PGD diminishes the fitness of H. pylori in vivo, but the pathway is nonessential for colonization.

Validation of Comet assay in Oregon-R and Wild type strains of Drosophila melanogaster exposed to a natural radioactive environment in Brazilian semiarid region

2017 ◽  
Vol 141 ◽  
pp. 148-153 ◽  
Author(s):  
Cícero Jorge Verçosa ◽  
Aroldo Vieira de Moraes Filho ◽  
Ícaro Fillipe de Araújo Castro ◽  
Robson Gomes dos Santos ◽  
Kenya Silva Cunha ◽  
...  
Keyword(s):  
Drosophila Melanogaster ◽  
Comet Assay ◽  
Semiarid Region ◽  
Wild Type ◽  
Brazilian Semiarid ◽  
Type Strains

scholarly journals Role of Streptococcus gordoniiAmylase-Binding Protein A in Adhesion to Hydroxyapatite, Starch Metabolism, and Biofilm Formation

2001 ◽  
Vol 69 (11) ◽  
pp. 7046-7056 ◽  
Author(s):  
Jeffrey D. Rogers ◽  
Robert J. Palmer ◽  
Paul E. Kolenbrander ◽  
Frank A. Scannapieco
Keyword(s):  
Biofilm Formation ◽  
Binding Protein ◽  
Protein A ◽  
Scatchard Analysis ◽  
Wild Type ◽  
Salivary Amylase ◽  
Carbohydrate Source ◽  
Whole Saliva ◽  
Mutant Strains ◽  
Type Strains

ABSTRACT Interactions between bacteria and salivary components are thought to be important in the establishment and ecology of the oral microflora. α-Amylase, the predominant salivary enzyme in humans, binds to Streptococcus gordonii, a primary colonizer of the tooth. Previous studies have implicated this interaction in adhesion of the bacteria to salivary pellicles, catabolism of dietary starches, and biofilm formation. Amylase binding is mediated at least in part by the amylase-binding protein A (AbpA). To study the function of this protein, an erythromycin resistance determinant [erm(AM)] was inserted within the abpAgene of S. gordonii strains Challis and FAS4 by allelic exchange, resulting in abpA mutant strains Challis-E1 and FAS4-E1. Comparison of the wild-type and mutant strains did not reveal any significant differences in colony morphology, biochemical metabolic profiles, growth in complex or defined media, surface hydrophobicity, or coaggregation properties. Scatchard analysis of adhesion isotherms demonstrated that the wild-type strains adhered better to human parotid-saliva- and amylase-coated hydroxyapatite than did the AbpA mutants. In contrast, the mutant strains bound to whole-saliva-coated hydroxyapatite to a greater extent than did the wild-type strains. While the wild-type strains preincubated with purified salivary amylase grew well in defined medium with potato starch as the sole carbohydrate source, the AbpA mutants did not grow under the same conditions even after preincubation with amylase. In addition, the wild-type strain produced large microcolonies in a flow cell biofilm model, while the abpA mutant strains grew much more poorly and produced relatively small microcolonies. Taken together, these results suggest that AbpA ofS. gordonii functions as an adhesin to amylase-coated hydroxyapatite, in salivary-amylase-mediated catabolism of dietary starches and in human saliva-supported biofilm formation by S. gordonii.

scholarly journals Overexpression of an activated rasG gene during growth blocks the initiation of Dictyostelium development.

1996 ◽  
Vol 16 (8) ◽  
pp. 4156-4162 ◽  
Author(s):  
M Khosla ◽  
G B Spiegelman ◽  
G Weeks
Keyword(s):  
Growth Rate ◽  
Cell Growth ◽  
Cyclic Amp ◽  
Dominant Negative ◽  
Differentiation Process ◽  
Fruiting Bodies ◽  
Wild Type ◽  
Ras Protein ◽  
Initial Generation ◽  
Type Strains

Transformants that expressed either the wild-type rasG gene, an activated rasG-G12T gene, or a dominant negative rasG-S17N gene, all under the control of the folate-repressible discoidin (dis1gamma) promoter, were isolated. All three transformants expressed high levels of Ras protein which were reduced by growth in the presence of folate. All three transformants grew slowly, and the reduction in growth rate correlated with the amount of RasG protein produced, suggesting that RasG is important in regulating cell growth. The pVEII-rasG transformant containing the wild-type rasG gene developed normally despite the presence of high levels of RasG throughout development. This result indicates that the down regulation of rasG that normally occurs during aggregation of wild-type strains is not essential for the differentiation process. Dictyostelium transformants expressing the dominant negative rasG-S17N gene also differentiated normally. Dictyostelium transformants that overexpressed the activated rasG-G12T gene did not aggregate. The defect occurred very early in development, since the expression of car1 and pde, genes that are normally induced soon after the initiation of development, was repressed. However, when the transformant cells were pulsed with cyclic AMP, expression of both genes returned to wild-type levels. The transformants exhibited chemotaxis to cyclic AMP, and development was synergized by mixing with wild-type cells. Furthermore, cells that were pulsed with cyclic AMP for 4 h before being induced to differentiate by plating on filters produced small, but otherwise normal, fruiting bodies. These results suggest that the rasG-G12T transformants are defective in cyclic AMP production and that RasG - GTP blocks development by interfering with the initial generation of cyclic AMP pulses.

scholarly journals Slow or stepped rewarming after acute low-temperature exposure does not improve survival of Drosophila melanogaster larvae

2008 ◽  
Vol 140 (3) ◽  
pp. 306-311 ◽  
Author(s):  
Brent J. Sinclair ◽  
Arun Rajamohan
Keyword(s):  
Drosophila Melanogaster ◽  
Low Temperature ◽  
Wild Type ◽  
General Increase ◽  
Larval Stages ◽  
Rapid Cold Hardening ◽  
Temperature Exposure ◽  
Low Temperature Exposure ◽  
Slow Fashion ◽  
Type Strains

AbstractWe tested the hypothesis that slow rewarming would improve the ability of Drosophila melanogaster Meigen (Diptera: Drosophilidae) larvae to survive acute low-temperature exposure. Four larval stages (1st, 2nd, and 3rd instars, including wandering-stage 3rd instars) of four wild-type strains were exposed to –7 °C for periods of time expected to result in 90% mortality. Larvae were then directly transferred to their rearing temperature (21 °C) or returned to this temperature either in a stepwise fashion (pausing at 0 and 15 °C) or by slow warming at 1 or 0.1 °C/min. We observed a reduced rapid cold-hardening effect and no general increase in survival of acute chilling in larvae rewarmed in a stepwise or slow fashion, and we hypothesize that slow rewarming may result in accumulation of chill injuries.

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