scholarly journals Confirmation of Apparent Genetic Assimilation of Behaviour in Drosophila melanogaster

Nature ◽  
1964 ◽  
Vol 204 (4957) ◽  
pp. 504-504 ◽  
Author(s):  
P. ARNOLD ◽  
N. MORAY
Keyword(s):  
Drosophila Melanogaster ◽  
Genetic Assimilation

scholarly journals Genetic assimilation of part of a mutant phenotype

1975 ◽  
Vol 26 (2) ◽  
pp. 149-162 ◽  
Author(s):  
James N. Thompson ◽  
J. M. Thoday
Keyword(s):  
Drosophila Melanogaster ◽  
Selection Response ◽  
Mutant Phenotype ◽  
Genetic Assimilation ◽  
Selection Line ◽  
Gap Formation ◽  
Vein Pattern ◽  
Chromosome Ii

SUMMARYWhen the mutant veinlet was removed from a Drosophila melanogaster line selected for shortened vein length it was found that the selected polygenic background produced vein gaps in the absence of the major mutant. This example of genetic assimilation was unusual, however, in that the phenotype of the assimilated line was not exactly the same as the phenotype of the original selection line. It differed in two respects: only one of the longitudinal veins was affected in the assimilation line whereas all veins are shortened in the selected ve line, and vein gaps were sub-terminal in the assimilated line whereas they are terminal in veinlet. Modifiers of L 4 vein length were found to be located on both chromosomes II and III, though the chromosome II factor had a larger effect and was required for gap formation. The chromosome II gene was mapped to the same position as a similar L 4 vein length polygene (PL(2)L4a) found in another veinlet selection line and reported elsewhere. The pattern of expression of the ve mutant and the assimilated line genotype were compared using profiles of vein frequency at given points. The vein pattern profiles are discussed in relation to an hypothesis to explain the observed selection response and the effectiveness which these polygene combinations showed in modifying the much more complex veinlet phenotype.

Author response for "Location and arrangement of campaniform sensilla in Drosophila melanogaster"

2020 ◽  
Author(s):  
Gesa F. Dinges ◽  
Alexander S. Chockley ◽  
Till Bockemühl ◽  
Kei Ito ◽  
Alexander Blanke ◽  
...  
Keyword(s):  
Drosophila Melanogaster ◽  
Author Response ◽  
Campaniform Sensilla

Live Confocal Analysis of Fertilization and Early Development

2001 ◽  
Vol 7 (S2) ◽  
pp. 1012-1013
Author(s):  
Uyen Tram ◽  
William Sullivan
Keyword(s):  
Drosophila Melanogaster ◽  
Embryonic Development ◽  
Real Time ◽  
Early Development ◽  
Fluorescent Probes ◽  
Primary Defect ◽  
Fluorescent Analysis ◽  
Dynamic Event ◽  
Enormous Amount ◽  
Fluorescent Studies

Embryonic development is a dynamic event and is best studied in live animals in real time. Much of our knowledge of the early events of embryogenesis, however, comes from immunofluourescent analysis of fixed embryos. While these studies provide an enormous amount of information about the organization of different structures during development, they can give only a static glimpse of a very dynamic event. More recently real-time fluorescent studies of living embryos have become much more routine and have given new insights to how different structures and organelles (chromosomes, centrosomes, cytoskeleton, etc.) are coordinately regulated. This is in large part due to the development of commercially available fluorescent probes, GFP technology, and newly developed sensitive fluorescent microscopes. For example, live confocal fluorescent analysis proved essential in determining the primary defect in mutations that disrupt early nuclear divisions in Drosophila melanogaster. For organisms in which GPF transgenics is not available, fluorescent probes that label DNA, microtubules, and actin are available for microinjection.

Apoptosis and development

2003 ◽  
Vol 39 ◽  
pp. 11-24 ◽  
Author(s):  
Justin V McCarthy
Keyword(s):  
Drosophila Melanogaster ◽  
Mammalian Cells ◽  
Cell Number ◽  
Model Organisms ◽  
Biological Processes ◽  
Nematode Caenorhabditis Elegans ◽  
Apoptotic Pathway ◽  
Genetic Pathways ◽  
Evolutionarily Conserved ◽  
Multicellular Organisms

Apoptosis is an evolutionarily conserved process used by multicellular organisms to developmentally regulate cell number or to eliminate cells that are potentially detrimental to the organism. The large diversity of regulators of apoptosis in mammalian cells and their numerous interactions complicate the analysis of their individual functions, particularly in development. The remarkable conservation of apoptotic mechanisms across species has allowed the genetic pathways of apoptosis determined in lower species, such as the nematode Caenorhabditis elegans and the fruitfly Drosophila melanogaster, to act as models for understanding the biology of apoptosis in mammalian cells. Though many components of the apoptotic pathway are conserved between species, the use of additional model organisms has revealed several important differences and supports the use of model organisms in deciphering complex biological processes such as apoptosis.

Insights into amyloid disease from fly models

2014 ◽  
Vol 56 ◽  
pp. 69-83 ◽  
Author(s):  
Ko-Fan Chen ◽  
Damian C. Crowther
Keyword(s):  
Drosophila Melanogaster ◽  
Neurodegenerative Disorders ◽  
Amyloid Β ◽  
Amyloid Β Peptide ◽  
Disease Pathogenesis ◽  
Amyloid Aggregates ◽  
Aβ Amyloid ◽  
Polypeptide Chains ◽  
Amyloid Diseases

The formation of amyloid aggregates is a feature of most, if not all, polypeptide chains. In vivo modelling of this process has been undertaken in the fruitfly Drosophila melanogaster with remarkable success. Models of both neurological and systemic amyloid diseases have been generated and have informed our understanding of disease pathogenesis in two main ways. First, the toxic amyloid species have been at least partially characterized, for example in the case of the Aβ (amyloid β-peptide) associated with Alzheimer's disease. Secondly, the genetic underpinning of model disease-linked phenotypes has been characterized for a number of neurodegenerative disorders. The current challenge is to integrate our understanding of disease-linked processes in the fly with our growing knowledge of human disease, for the benefit of patients.

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