3 research outputs found
Echinus does not require deubiquitinating activity to promote normal IOC death
<p><b>Copyright information:</b></p><p>Taken from ", required for interommatidial cell sorting and cell death in the pupal retina, encodes a protein with homology to ubiquitin-specific proteases"</p><p>http://www.biomedcentral.com/1471-213X/7/82</p><p>BMC Developmental Biology 2007;7():82-82.</p><p>Published online 5 Jul 2007</p><p>PMCID:PMC1950886.</p><p></p> (A-D) SEMs of adult eyes of various genotypes. (E-H) Pupal retinas of various genotypes stained with anti-Dlg. (A,E) GMR-driven expression of a microRNA targeting ec-SF1 results in an echinus phenotype. (B,F) eyes. (C,G) Eyes of genotype ; GMR-ec-SF2/+. (D,H) Eyes of genotype ; GMR-ec-SF3/+. Expression of versions of Echinus that lack essential USP catalytic residues rescues the phenotype
Flies with mutations in CG2904 have rough eyes, defects in IOC sorting, an increase in IOC number (A-F) SEM views of adult fly eyes of various genotypes
<p><b>Copyright information:</b></p><p>Taken from ", required for interommatidial cell sorting and cell death in the pupal retina, encodes a protein with homology to ubiquitin-specific proteases"</p><p>http://www.biomedcentral.com/1471-213X/7/82</p><p>BMC Developmental Biology 2007;7():82-82.</p><p>Published online 5 Jul 2007</p><p>PMCID:PMC1950886.</p><p></p> (G-O) Pupal retinas of various genotypes stained with anti-Dlg. (A, G) Wildtype flies have regularly spaced ommatidia and an invariant number of IOCs. Cell types indicated are bristle (B), 2°, 3°, and asterisk represent extra IOCs. (B,H) flies obtained from the Bloomington Stock center have rough eyes and a modest number of extra 2° and 3° pigment cells. (C,I) GMR-driven RNAi of CG2904 results in flies with rough eyes and a large increase in IOCs, with many stacked side-by-side in parallel rows. (D,J) Flies homozygous for a deletion in CG2904, , have rough eyes, a large increase in IOCs, with many cells stacked side-by-side in parallel rows. (E,K) GMR-dependent expression of ec-SF1 has no effect on the adult eye and does not cause any excess death of IOCs. (F,L) Expression of GMR-ec-SF1 restores normal levels of IOC death to flies. (M,N) Pupal eyes from two independent stocks of outcrossed for 5 generations. There are increased numbers of IOCs as compared with the original stock, and many extra cells are aligned side-by-side in parallel rows. (O) Pupal eyes from flies have a modest increase in IOC number and few defects in cell sorting
Genetic interactions between and known or potential regulators of cell death in the eye
<p><b>Copyright information:</b></p><p>Taken from ", required for interommatidial cell sorting and cell death in the pupal retina, encodes a protein with homology to ubiquitin-specific proteases"</p><p>http://www.biomedcentral.com/1471-213X/7/82</p><p>BMC Developmental Biology 2007;7():82-82.</p><p>Published online 5 Jul 2007</p><p>PMCID:PMC1950886.</p><p></p> To the right is a schematic depicting known or suggested interactions between death regulators in the fly. The question mark separating Debcl/Buffy from Ark indicates the uncertainy as to the roles these proteins play in regulating Ark activation or activity. GMR-driven transgenes of the indicated genotype were introduced into the background, or into a wildtype background in the presence of GMR-ec-SF1. For each death regulator tested, similar phenotypes were observed in the presence of GMR-ec-SF2 (data not shown)