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M B Sokolowski

Publications and source records attributed to M B Sokolowski.

34 records · Page 2Linked to original sources

Chaser (Csr), a new gene affecting larval foraging behavior in Drosophila melanogaster.

Chaser (Csr) was uncovered in a gamma mutagenesis screen to identify genes that modify the larval foraging behavior of sitters to rovers. Rover larvae have significantly longer path lengths than sitters while foraging on a yeast and water paste. This difference is influenced by one major gene, foraging (for), which has two naturally occurring alleles, forR (rover) and fors (sitter). In a mutagenesis screen for modifiers of for, we identified three lines with viable mutations on chromosome 3 that alter foraging behavior. Each of these mutations increased larval path lengths in fors/fors larvae in a dominant fashion, and were not separable by recombination. These mutations are therefore probably allelic and define a new gene that we have called Csr. Csr was genetically localized using the lethal-tagging technique. This technique resulted in seven lines with a significant decrease in larval path-length and recessive lethal mutations on chromosome 3. We refer to these as reverted Csr (Csrrv) lines. Deficiencies that uncovered cytologically visible chromosome rearrangements in three of the seven reverted lines were used in a complementation analysis. In this way we mapped the lethal mutations in the Csrrv lines to cytological region 95F7-96A1 on the right arm of chromosome 3.

Alleles↗

Characterization and genetic analysis of Drosophila melanogaster photobehavior during larval development.

In Drosophila melanogaster, during the mid third instar of development larvae cease foraging and commence a period of increased locomotor activity referred to as wandering behavior. In this study, we quantified the wild type larval response to light during the foraging (first, second, and early third instars) and wandering (late third instar) stages of development. Foraging larvae in the first, second and early third instars exhibited a robust and marked aversion to light (negative phototaxis). From the mid larval third instar larvae showed a decrease in photonegative behavior, until just before pupation when the response of wandering larvae to light became random. The photobehavior of several strains known to affect the adult visual system were also studied. All but four exhibited normal phototaxis in the foraging and wandering stages. gl mutant larvae failed to respond to light during the foraging stage likely due to lack of larval photoreceptors. Larvae carrying three different mutations in the rhodopsin RH1 gene continued to express negative phototaxis throughout both the foraging and wandering stages. These results suggest that the transition from negative phototaxis toward photoneutral behavior characteristic of the wandering third instar larva requires vision.

Animals↗

Mutations in the larval foraging gene affect adult locomotory behavior after feeding in Drosophila melanogaster.

Previous studies have shown a correlation between the locomotory component of larval and adult foraging behavior in the fruit fly. Here we show that this relationship is far more than mere correlation. It can be attributable to different alleles at the same genetic locus of the behavioral gene foraging (for). The for gene offers us the unique opportunity to study the genetic basis and evolutionary significance of a naturally occurring behavioral polymorphism. Until now, only the effect of for on Drosophila melanogaster larval behavior was studied. Larvae with the rover allele (forR) move significantly more while eating during a set time period than those homozygous for the sitter alleles (fors). Here, we show that rover and sitter larval strains derived from nature differ in the distance adults walk after feeding per unit time and that this variation results from different alleles at the foraging locus, the very gene originally defined on the basis of larval behavior. We hypothesize that for may be involved in the way flies evaluate a food resource.

Alleles↗

Diapause in Drosophila melanogaster females: a genetic analysis.

Female Drosophila melanogaster exhibit ovarian diapause at low temperatures and short day lengths. We found that D. melanogaster isofemale lines from Windsor (Ontario, Canada) had a significantly higher percentage of females in diapause than did those from Cartersville (Georgia, U.S.A.). To investigate the heredity of this trait, we performed a 16-reciprocal cross analysis using two extreme isofemale lines called W and C. We found that diapause in D. melanogaster is inherited as a simple autosomal recessive trait with the C response (less flies in diapause) completely dominant to the W one. Maternal and cytoplasmic factors did not affect differences in diapause in these lines. The result of our genetic analysis of diapause in D. melanogaster opens may avenues for the genetic dissection of this ecologically relevant trait.

Adaptation, Physiological↗

Genetic analysis of the foraging microregion of Drosophila melanogaster.

The rover/sitter polymorphism in Drosophila melanogaster larval behaviour is a unique example of a genetically determined, naturally occurring behavioural polymorphism. Allelic variation at the foraging locus (for) accounts for the rover (long foraging paths) and sitter (short foraging paths) phenotypes. We previously developed lethal tagging and used deficiency mapping to place for in the 24A3-C5 interval on the polytene chromosome map, thereby defining the for microregion. Here, we subjected this microregion to mutational analysis to (i) isolate putative lethal foraging mutations and characterize their behavioural phenotypes to assess whether or not for is a vital locus, (ii) generate cytologically detectable chromosome rearrangements with breakpoints in or near for for more precise localization and for future molecular analysis of the for gene, and (iii) identify other gene loci in the immediate vicinity of the for locus. We recovered 10 gamma-induced and 33 ethyl methanesulfonate (EMS) induced new mutations that define seven complementation groups in 24A3-D4. Two new EMS-induced lethal for alleles and four gamma-induced rearrangements with breakpoints in for were identified, which allowed us to further localize for to 24A3-5. All lethal mutations in for resulted in an altered behavioural phenotype providing evidence that both vital and behavioural functions are encoded by for.

Alleles↗

The foraging locus: behavioral tests for normal muscle movement in rover and sitter Drosophila melanogaster larvae.

We used Drosophila melanogaster larvae with different alleles at the foraging (for) locus in a variety of behavioral tests to evaluate normal muscle usage of rover and sitter phenotypes. The results show that sitter and lethal sitter alleles of for do not affect larval behavior through a mutation which affects larval muscle usage. In general the behavior of rovers and sitters differed on food but not on non-nutritive substrates. Rovers and sitters moved equally well on non-nutritive substrates, and measures such as the time to roll over and length of forward stride showed no significant strain differences. Larvae with different alleles at for did not differ in body length. Rovers took more strides, not longer ones, than sitters while on foraging substrates. We conclude that differences in larval locomotion during foraging found in larvae with different alleles at for can not be explained on the basis of muscle usage alone. It is more likely that for affects larval ability to perceive or respond to the foraging environment.

Alleles↗

Genetic analyses of pupation distance in Drosophila melanogaster.

The inheritance of Drosophila melanogaster larval pupation behaviour is investigated in sixteen reciprocal crosses between field collected lines. These lines were made isogenic for the two major autosomes enabling the data to be analyzed using contrast analysis of variance and biometrical genetic analysis. Results of both analyses showed that the trait "pupation distance", the distance larvae pupate from food, fits a simple additive model of inheritance with no dominance. A chromosomal analysis showed that both the second and third chromosomes act additively on pupation distance and that the third pair of chromosomes had a much larger effect than the second. Significant variability exists in the distance D. melanogaster larvae pupate from fruit in nature. This phenotypic variation results from both heritable variation and variation from environmental sources. When the moisture content of the environment surrounding food is modified, gene by environment interactions also contribute to variation in the phenotype. Selective pressures which may act on larval differences in pupation site choice are discussed.

Analysis of Variance↗

Genetic localization of foraging (for): a major gene for larval behavior in Drosophila melanogaster.

Localizing genes for quantitative traits by conventional recombination mapping is a formidable challenge because environmental variation, minor genes, and genetic markers have modifying effects on continuously varying phenotypes. We describe "lethal tagging," a method used in conjunction with deficiency mapping for localizing major genes associated with quantitative traits. Rover/sitter is a naturally occurring larval foraging polymorphism in Drosophila melanogaster which has a polygenic pattern of inheritance comprised of a single major gene (foraging) and minor modifier genes. We have successfully localized the lethal tagged foraging (for, 2-10) gene by deficiency mapping to 24A3-C5 on the polytene chromosome map.

Animals↗

Foraging strategies of Drosophila melanogaster: a chromosomal analysis.

Two larval foraging strategies in Drosophila melanogaster were identified, "rover" and "sitter." "Rovers" traverse a large area while feeding whereas "sitters" cover a small area. The difference between "rovers" and "sitters" was analyzed genetically by chromosomal substitutions between isogenic stocks. Differences in larval locomotor behavior ("crawling behavior") can be attributed to the second chromosome, the "rover" strategy being dominant over the "sitter" strategy. Differences in feeding rate ("shoveling behavior") are affected additively by both the second and third chromosomes. Natural populations of Drosophila larvae were sampled three times over a 2-month period; "rovers" and "sitters" were at constant frequencies in these populations. The two foraging strategies are discussed in the light of resource utilization in environments where food is distributed continuously or discontinuously.

Animals↗

The supposed role of micro-biological aerosol stabilizers as substitutes for bound water: a study of an in vitro model system.

In order to test a suggestion that inositol may take the place of water in maintaining the stability of desiccated cells, the reversible endothermic association of tobacco mosaic virus protein (TMVP) was studied turbidimetrically in presence of this substance. Its effect was to lower the temperature at which association takes place, the positive standard enthalpy and standard entropy of reaction both being increased by about 30%. The hypothesis of direct substitution of bound water by inositol at the site of macromolecular association leads to the contrary prediction that the association temperature would be raised. It is suggested that the observed effect of inositol may result from a conformation change in TMVP brought about by binding of inositol at positions adjacent to the site of reaction.

Aerosols↗

A cGMP-dependent protein kinase gene, foraging, modifies habituation-like response decrement of the giant fiber escape circuit in Drosophila.

The Drosophila giant fiber jump-and-flight escape response is a model for genetic analysis of both the physiology and the plasticity of a sensorimotor behavioral pathway. We previously established the electrically induced giant fiber response in intact tethered flies as a model for habituation, a form of nonassociative learning. Here, we show that the rate of stimulus-dependent response decrement of this neural pathway in a habituation protocol is correlated with PKG (cGMP-Dependent Protein Kinase) activity and foraging behavior. We assayed response decrement for natural and mutant rover and sitter alleles of the foraging (for) gene that encodes a Drosophila PKG. Rover larvae and adults, which have higher PKG activities, travel significantly farther while foraging than sitters with lower PKG activities. Response decrement was most rapid in genotypes previously shown to have low PKG activities and sitter-like foraging behavior. We also found differences in spontaneous recovery (the reversal of response decrement during a rest from stimulation) and a dishabituation-like phenomenon (the reversal of response decrement evoked by a novel stimulus). This electrophysiological study in an intact animal preparation provides one of the first direct demonstrations that PKG can affect plasticity in a simple learning paradigm. It increases our understanding of the complex interplay of factors that can modulate the sensitivity of the giant fiber escape response, and it defines a new adult-stage phenotype of the foraging locus. Finally, these results show that behaviorally relevant neural plasticity in an identified circuit can be influenced by a single-locus genetic polymorphism existing in a natural population of Drosophila.

Animals↗