The dominant Drop eye mutations of Drosophila melanogaster define two loci implicated in normal eye development

1994 ◽  
Vol 244 (4) ◽  
pp. 426-434 ◽  
Author(s):  
Rick Tearle ◽  
Andrew Tomlinson ◽  
Robert Saint
1971 ◽  
Vol 17 (3) ◽  
pp. 195-208 ◽  
Author(s):  
David M. Hunt

SUMMARYThe effect of dietary supplements of individual l-amino acids on the expression of the eyegone and eyelessK mutants of Drosophila melanogaster are compared. In both mutants, eye size is reduced by excess levels of tryptophan, phenylalanine and methionine, and in each case the effects are independent of metabolic competition for pyridoxal phosphate. A dietary interaction involving methionine and UNA can be demonstrated in the eyK strain, but the mechanism of action of this amino acid is obscure. Tryptophan metabolism is examined in detail. Although both tryptamine and serotonin have significant effects, the action of tryptophan on eye development is largely independent of its metabolic products. Conversely, the effect of dietary supplements of certain catecholamines is consistent with the action of phenylalanine. The action of certain metabolic inhibitors provides additional support for the suggestion that the catecholamines have an important effect on morphogenesis in the eye imaginai disks. Eye development is also affected by increasing concentrations of γ-amino-butyric acid, and this, taken together with the effect of the catecholamines and indolalkylamines, suggests that physiological control of the action of the mutant genes on eye development involves a group of compounds characteristically associated with nervous tissue. Eye development in the eyK strain may be influenced by the availability of acetyl CoA, which would be expected to affect acetylcholine biosynthesis. Possible mechanisms of action of the effective dietary treatments are discussed, together with a tentative hypothesis regarding the mode of action of the mutant genes on eye development.


1969 ◽  
Vol 13 (3) ◽  
pp. 313-320 ◽  
Author(s):  
David M. Hunt

A comparison of the gene-environment interactions of the eyg mutant in two different genetic backgrounds clearly demonstrates that the properties of the genetic background play a major role in the control of the gene-environment interactions of this mutant. Similarly, modifier background is important in the determination of the sensitive stages in eye development to a cholesterol-deficient diet.The phenotypic identity of the eyeless and eye-gone mutants suggests a close underlying metabolic and developmental relationship. Possible inter-relations of these two mutant genes are discussed in the light of their gene-environment interactions in a standardized genotype.


Development ◽  
2012 ◽  
Vol 139 (8) ◽  
pp. e808-e808
Author(s):  
S. Kametaka ◽  
A. Kametaka ◽  
S. Yonekura ◽  
M. Haruta ◽  
S. Takenoshita ◽  
...  

2019 ◽  
Vol 9 (7) ◽  
pp. 2061-2070 ◽  
Author(s):  
Rose C. Pletcher ◽  
Sara L. Hardman ◽  
Sydney F. Intagliata ◽  
Rachael L. Lawson ◽  
Aumunique Page ◽  
...  

2012 ◽  
Vol 348 (3) ◽  
pp. 453-463 ◽  
Author(s):  
Dang Thi Phuong Thao ◽  
Phan Nguyen Thuy An ◽  
Masamitsu Yamaguchi ◽  
Tran LinhThuoc

2020 ◽  
Vol 249 (9) ◽  
pp. 1147-1165 ◽  
Author(s):  
Brett W. Gershman ◽  
Caroline E. Pritchard ◽  
Kenneth P. Chaney ◽  
Vassie C. Ware

2020 ◽  
Vol 21 (11) ◽  
pp. 4086
Author(s):  
Tuan L. A. Pham ◽  
Tran Duy Binh ◽  
Guanchen Liu ◽  
Thanh Q. C. Nguyen ◽  
Yen D. H. Nguyen ◽  
...  

Serotonin transporter (SerT) in the brain is an important neurotransmitter transporter involved in mental health. However, its role in peripheral organs is poorly understood. In this study, we investigated the function of SerT in the development of the compound eye in Drosophila melanogaster. We found that SerT knockdown led to excessive cell death and an increased number of cells in S-phase in the posterior eye imaginal disc. Furthermore, the knockdown of SerT in the eye disc suppressed the activation of Akt, and the introduction of PI3K effectively rescued this phenotype. These results suggested that SerT plays a role in the healthy eye development of D. melanogaster by controlling cell death through the regulation of the PI3K/Akt pathway.


Author(s):  
Trang Thi Thuy Cao ◽  
Thao Thi Phuong Dang

Human ubiquitin carboxyl-terminal hydrolase L1 (UCH-L1) is a member of deubiquitinating enzyme group and a component of ubiquitin-proteasome system. Being one of the neuron-specific proteins, abnormalities of UCH-L1 was observed in several neurodegenerative diseases such as Parkinson’s disease and Alzheimer’s disease. On the other hand, UCH-L1 was also found to be present in various kinds of cancers with inconsistent acting reported in different studies. Together these records indicated the involvement of UCH-L1 in maintaining normal activities of cells, tissues and organs. However, in vivo significance of the protein remains unclear. In addition, among the attempts made to approach the biological function of UCHL1, there has been no previous report addressing its part in development. In order to explore the function of UCH-L1, we utilized Drosophila melanogaster as model to investigate effects of dUCH (a Drosophila homologue of human UCH-L1) on the development. Particularly in Drosophila eye development, in this study. Our experimental results revealed that specific overexpression of dUCH in eye tissue induced the disruption in ommatidia orientation and defects in differentiation of pigment cells. These results are evidence that support the role of dUCH as a development mediating factor.


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