Genetic analysis of body color phenotypes in the fruit fly Drosophila melanogaster: supporting evidence through laboratory-selected dark and light strains

2012 ◽  
Vol 90 (5) ◽  
pp. 564-576 ◽  
Author(s):  
Ravi Parkash ◽  
Seema Ramniwas ◽  
Babita Kajla

In the fruit fly Drosophila melanogaster Meigen, 1830, abdominal melanisation varies in a quantitative manner, but little attention has been paid to the genetic basis of different phenotypic classes and their ecological significance in the wild populations. Laboratory-selected darker and lighter body color strains were used for determining the genetic basis of body color phenotypes. Based on such genetic characterization, we interpreted body color variation of wild flies collected along a latitudinal gradient. Our results are interesting in several respects. First, laboratory selection produced lighter females and also lighter males, in contradiction of the well-known sexual dimorphism in D. melanogaster. The laboratory-selected darker and lighter strains showed lack of phenotypic plasticity, whereas F1 flies from reciprocal crosses showed significant levels of phenotypic plasticity. Second, for both sexes, F2 phenotypic classes resulting from reciprocal crosses between selected darker and lighter strains fit a two-locus model with a stronger maternal effect in males than in females. Third, changes in continuously varying abdominal melanisation of wild-caught flies were sorted into phenotypic bins of body color phenotypic classes and such data on geographical populations of D. melanogaster are consistent with climatic selection. Thus, we may suggest that for ecological genetic studies, greater emphasis should be laid on the analysis of bins of phenotypic classes of body melanisation in laboratory and wild populations of D. melanogaster.

2017 ◽  
Author(s):  
Catherine R. Linnen ◽  
Claire T. O’Quin ◽  
Taylor Shackleford ◽  
Connor R. Sears ◽  
Carita Lindstedt

ABSTRACTPigmentation has emerged as a premier model for understanding the genetic basis of phenotypic evolution, and a growing catalog of color loci is starting to reveal biases in the mutations, genes, and genetic architectures underlying color variation in the wild. However, existing studies have sampled a limited subset of taxa, color traits, and developmental stages. To expand our sample of color loci, we performed quantitative trait locus (QTL) mapping analyses on two types of larval pigmentation traits that vary among populations of the redheaded pine sawfly (Neodiprion lecontei): carotenoid-based yellow body color and melanin-based spotting pattern. For both traits, our QTL models explained a substantial proportion of phenotypic variation and suggested a genetic architecture that is neither monogenic nor highly polygenic. Additionally, we used our linkage map to anchor the current N. lecontei genome assembly. With these data, we identified promising candidate genes underlying: (1) a loss of yellow pigmentation in Mid-Atlantic/northeastern populations (Cameo2 and apoLTP-II/I), and (2) a pronounced reduction in black spotting in Great-Lakes populations (yellow, TH, Dat). Several of these genes also contribute to color variation in other wild and domesticated taxa. Overall, our findings are consistent with the hypothesis that predictable genes of large-effect contribute to color evolution in nature.


2011 ◽  
Vol 49 ◽  
pp. 19-35 ◽  
Author(s):  
Nicholas R. J Glossop

The discovery of the period gene mutants in 1971 provided the first evidence that daily rhythms in the sleep–wake cycle of a multicellular organism, the fruit fly Drosophila melanogaster, had an underlying genetic basis. Subsequent research has established that the biological clock mechanism in flies and mammals is strikingly similar and functions as a bimodal switch, simultaneously turning on one set of genes and turning off another set and then reversing the process every 12 h. In this chapter, the current model of the clock mechanism in Drosophila will be presented. This relatively basic model will then be used to outline the general rules that govern how the biological clock operates in mammals.


2018 ◽  
Vol 12 (4) ◽  
pp. 959-972 ◽  
Author(s):  
Karen L. Adair ◽  
Marita Wilson ◽  
Alyssa Bost ◽  
Angela E. Douglas

2019 ◽  
Author(s):  
Mirko Pegoraro ◽  
Laura M.M. Flavell ◽  
Pamela Menegazzi ◽  
Perrine Colombi ◽  
Pauline Dao ◽  
...  

Abstract Background Most animals restrict their activity to a specific part of the day, being diurnal, nocturnal or crepuscular. The genetic basis underlying diurnal preference is largely unknown. Under laboratory conditions, Drosophila melanogaster is crepuscular, showing a bi-modal activity profile. However, a survey of strains derived from wild populations indicated that high variability among individuals exists, including flies that are nocturnal.Results Using a highly diverse population, we have carried out an artificial selection experiment, selecting flies with extreme diurnal or nocturnal preference. After 10 generations, we obtained highly diurnal and nocturnal strains. We used whole-genome expression analysis to identify differentially expressed genes in diurnal, nocturnal and crepuscular (control) flies. Other than one circadian clock gene ( pdp1 ), most differentially expressed genes were associated with either clock output ( pdf, to ) or input ( Rh3 , Rh2, msn ). This finding was congruent with behavioural experiments indicating that both light masking and the circadian pacemaker are involved in driving nocturnality.Conclusions Our study demonstrates that natural genetic variation in fly wild populations is contributing to substantial variation in diurnal preference. We identified candidate genes associated with diurnality/nocturnality, and the data emerging from our expression analysis and behavioural experiments suggest that both the clock and clock-independent pathways are involved in shaping diurnal preference. The diurnal and nocturnal selection strains provide us with a unique opportunity to understand the genetic architecture of diurnal preference.


1981 ◽  
Vol 117 (2) ◽  
pp. 133-146 ◽  
Author(s):  
Donald W. Pyle ◽  
Mark H. Gromko

2021 ◽  
Vol 12 (1) ◽  
Author(s):  
Rachel Paul ◽  
Guillaume Giraud ◽  
Katrin Domsch ◽  
Marilyne Duffraisse ◽  
Frédéric Marmigère ◽  
...  

AbstractFlying insects have invaded all the aerial space on Earth and this astonishing radiation could not have been possible without a remarkable morphological diversification of their flight appendages. Here, we show that characteristic spatial expression profiles and levels of the Hox genes Antennapedia (Antp) and Ultrabithorax (Ubx) underlie the formation of two different flight organs in the fruit fly Drosophila melanogaster. We further demonstrate that flight appendage morphology is dependent on specific Hox doses. Interestingly, we find that wing morphology from evolutionary distant four-winged insect species is also associated with a differential expression of Antp and Ubx. We propose that variation in the spatial expression profile and dosage of Hox proteins is a major determinant of flight appendage diversification in Drosophila and possibly in other insect species during evolution.


Author(s):  
Rubén Sancho ◽  
Ana Guillem-Amat ◽  
Elena López-Errasquín ◽  
Lucas Sánchez ◽  
Félix Ortego ◽  
...  

AbstractThe sterile insect technique (SIT) is widely used in integrated pest management programs for the control of the Mediterranean fruit fly (medfly), Ceratitis capitata. The genetic interactions between the released individuals from the genetic sexing strains (GSS), used for SIT applications worldwide, and wild individuals have not been studied. Under the hypothesis that a number of Vienna GSS individuals released to the field might not be completely sterile and may produce viable offspring, we have analyzed medfly Spanish field populations to evaluate the presence of Vienna strain genetic markers. To this goal, we have used contrasted nuclear and mitochondrial genetic markers, and two novel sets of nuclear polymorphisms with the potential to be markers to discriminate between Vienna and wild individuals. Nuclear Vienna markers located on the 5th chromosome of Vienna males have been found in 2.2% (19 from 875) of the Spanish wild medfly females captured at the area where SIT is applied. In addition, a female-inherited mitochondrial Vienna marker has been found in two from the 19 females showing nuclear Vienna markers. The detection of several of these markers in single individuals represents evidence of the introgression of Vienna strain into natural populations. However, alternative explanations as their presence at low frequency in wild populations in the studied areas cannot be fully discarded. The undesired release of non-fully sterile irradiated GSS individuals into the field and their interactions with wild flies, and the potential environmental implications should be taken into account in the application of the SIT.


Genetics ◽  
1974 ◽  
Vol 76 (2) ◽  
pp. 289-299
Author(s):  
Margaret McCarron ◽  
William Gelbart ◽  
Arthur Chovnick

ABSTRACT A convenient method is described for the intracistronic mapping of genetic sites responsible for electrophoretic variation of a specific protein in Drosophila melanogaster. A number of wild-type isoalleles of the rosy locus have been isolated which are associated with the production of electrophoretically distinguishable xanthine dehydrogenases. Large-scale recombination experiments were carried out involving null enzyme mutants induced on electrophoretically distinct wild-type isoalleles, the genetic basis for which is followed as a nonselective marker in the cross. Additionally, a large-scale recombination experiment was carried out involving null enzyme rosy mutants induced on the same wild-type isoallele. Examination of the electrophoretic character of crossover and convertant products recovered from the latter experiment revealed that all exhibited the same parental electrophoretic character. In addition to documenting the stability of the xanthine dehydrogenase electrophoretic character, this observation argues against a special mutagenesis hypothesis to explain conversions resulting from allele recombination studies.


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