Author(s)

Ashley Cosenza^1,2, Jacob D. Kagey^1*

¹Biology Department, University of Detroit Mercy, Detroit, MI, USA.
²Honors Program, University of Detroit Mercy, Detroit, MI, USA.

A Flp/FRT EMS mutagenesis screen was conducted in the eye of Drosophila melanogaster on chromosome 2R to identify negative regulators of cell growth and cell division. In addition to the EMS mutation in the mosaic eye, an ark loss of function allele (ark⁸²) was utilized to block apoptosis in the homozygous mutant cells, setting up a screen for conditional regulators of cell growth and cell division. In the present study, we focus on the characterization and mapping of one mutant that resulted from this screen, Cruella (cru). A cross between flies with the flippase enzyme directed to the developing eye and flies with the mutations cru, ark⁸², revealed an unusual phenotype that resulted in the homozygous mutant tissue appearing black, in contrast to the expected red. To map the location of this mutation, complementation tests against the Bloomington deficiency kit were conducted. Cru failed to complement previously characterized alleles of capping protein α (cpa). Thus, cpa^cru is a novel allele of cpa and displays phenotypes similar to previously characterized alleles such as cpa 107E, cpa 69E, and cpa^scrd . The human homolog, Cap Z, is conserved in humans and serves a similar role in act in filament regulation.

Capping Protein α, Apoptosis, Genetic Screen, Drosophila melanogaster

Cosenza, A. and D. Kagey, J. (2016) The Mapping and Characterization of Cruella (Cru), a Novel Allele of Capping Protein α (Cpa), Identified from a Conditional Screen for Negative Regulators of Cell Growth and Cell Division. Advances in Bioscience and Biotechnology, 7, 373-380. doi: 10.4236/abb.2016.710036.