scholarly journals The Effect of Adult Body Color Mutations upon the Larva of Drosophila Melanogaster

1941 ◽  
Vol 27 (6) ◽  
pp. 254-261 ◽  
Author(s):  
K. S. Brehme
Genetics ◽  
1981 ◽  
Vol 98 (4) ◽  
pp. 849B-869
Author(s):  
Andrew G Clark ◽  
Marcus W Feldman

ABSTRACT The effects of larval density on components of fertility fitness were investigated with two mutant lines of Drosophila melanogaster. The differences in adult body weight, wing length, larval survivorship and development time verified that flies reared at high density were resource limited. Experimental results indicate that: (1) relative fecundities of both sexes show density-dependent effects, (2) there is a strong density effect on male and female mating success, and (3) in general, there is a reduction in fecundity differences between genotypes at high density. These results imply that it may be important to consider fertility in models of density-dependent natural selection.


Biology Open ◽  
2019 ◽  
Vol 8 (12) ◽  
pp. bio047084 ◽  
Author(s):  
Meghan Barrett ◽  
Katherine Fiocca ◽  
Edward A. Waddell ◽  
Cheyenne McNair ◽  
Sean O'Donnell ◽  
...  

1992 ◽  
Vol 287 (1) ◽  
pp. 85-89 ◽  
Author(s):  
F J Silva ◽  
Y Bel ◽  
L M Botella ◽  
R G H Cotton ◽  
J Ferré

A monoclonal antibody raised against monkey liver phenylalanine hydroxylase (PAH) has been used to detect this protein in Drosophila melanogaster. A cross-reacting material (CRM) band of apparent molecular mass 50-52 kDa, equivalent to that deduced for the Drosophila melanogaster PAH protein based on the pah gene cDNA sequence, has been detected. This CRM was analysed throughout development and showed an equivalent pattern to that reported for PAH activity in this insect, with maxima at pupariation and at pharate adult formation. Distribution of this CRM in larval tissues, the haemolymph and the adult body is mainly restricted to the larval fat body and the adult head. Demonstration of this CRM as the PAH protein comes from the correlation between the decreased PAH enzyme activities of two mutant strains and their decreased amounts of CRM by Western blotting.


2019 ◽  
Author(s):  
Eric P Spana ◽  
Amanda B Abrams ◽  
Katharine T Ellis ◽  
Jason C Klein ◽  
Brandon T Ruderman ◽  
...  

The pigmentation mutation speck is a commonly used recombination marker characterized by a darkly pigmented region at the wing hinge. Identified in 1910 by Thomas Hunt Morgan, speck was characterized by Sturtevant as the most 'workable' mutant in the rightmost region of the second chromosome and eventually localized to 2-107.0 and 60C1-2. Though the first speck mutation was isolated over 115 years ago, speck is still not associated with any gene. Here, as part of an undergraduate-led research effort, we show that speck is encoded by the Arylalkylamine N-acetyltransferase 1 (AANAT1) gene. Both alleles from the Morgan lab contain a retrotransposon in exon 1 of the RB transcript of the AANAT1 gene. We have also identified a new insertion allele and generated multiple deletion alleles in AANAT1 that all give a strong speck phenotype. In addition, expression of AANAT1 RNAi constructs either ubiquitously or in the dorsal portion of the developing wing generates a similar speck phenotype. We find that speck alleles have additional phenotypes, including ectopic pigmentation in the posterior pupal case, leg joints, cuticular sutures and overall body color. We propose that the acetylated dopamine generated by AANAT1 decreases the dopamine pool available for melanin production. When AANAT1 function is decreased, the excess dopamine enters the melanin pathway to generate the speck phenotype.


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.


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