Faculty Opinions recommendation of Evolution of gene expression in the Drosophila melanogaster subgroup.

Author(s):  
Detlef Weigel
2003 ◽  
Vol 33 (2) ◽  
pp. 138-144 ◽  
Author(s):  
Scott A. Rifkin ◽  
Junhyong Kim ◽  
Kevin P. White

2013 ◽  
Vol 304 (3) ◽  
pp. R177-R188 ◽  
Author(s):  
Wendi S. Neckameyer ◽  
Kathryn J. Argue

Numerous studies have detailed the extensive conservation of developmental signaling pathways between the model system, Drosophila melanogaster, and mammalian models, but researchers have also profited from the unique and highly tractable genetic tools available in this system to address critical questions in physiology. In this review, we have described contributions that Drosophila researchers have made to mathematical dynamics of pattern formation, cardiac pathologies, the way in which pain circuits are integrated to elicit responses from sensation, as well as the ways in which gene expression can modulate diverse behaviors and shed light on human cognitive disorders. The broad and diverse array of contributions from Drosophila underscore its translational relevance to modeling human disease.


Cell ◽  
1982 ◽  
Vol 28 (1) ◽  
pp. 33-40 ◽  
Author(s):  
Elizabeth C. Raff ◽  
Margaret T. Fuller ◽  
Thomas C. Kaufman ◽  
Kenneth J. Kemphues ◽  
Jane E. Rudolph ◽  
...  

2015 ◽  
Vol 5 (12) ◽  
pp. 2843-2856 ◽  
Author(s):  
Florence Gutzwiller ◽  
Catarina R. Carmo ◽  
Danny E. Miller ◽  
Danny W. Rice ◽  
Irene L. G. Newton ◽  
...  

2018 ◽  
Vol 5 (8) ◽  
pp. 180458 ◽  
Author(s):  
Eva Jiménez-Guri ◽  
Karl R. Wotton ◽  
Johannes Jaeger

Gap genes are involved in segment determination during early development of the vinegar fly Drosophila melanogaster and other dipteran insects (flies, midges and mosquitoes). They are expressed in overlapping domains along the antero-posterior (A–P) axis of the blastoderm embryo. While gap domains cover the entire length of the A–P axis in Drosophila, there is a region in the blastoderm of the moth midge Clogmia albipunctata , which lacks canonical gap gene expression. Is a non-canonical gap gene functioning in this area? Here, we characterize tarsal-less ( tal ) in C. albipunctata . The homologue of tal in the flour beetle Tribolium castaneum (called milles-pattes, mlpt ) is a bona fide gap gene. We find that Ca-tal is expressed in the region previously reported as lacking gap gene expression. Using RNA interference, we study the interaction of Ca-tal with gap genes. We show that Ca-tal is regulated by gap genes, but only has a very subtle effect on tailless (Ca-tll), while not affecting other gap genes at all. Moreover, cuticle phenotypes of Ca-tal depleted embryos do not show any gap phenotype. We conclude that Ca-tal is expressed and regulated like a gap gene, but does not function as a gap gene in C. albipunctata .


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