Amino acids 339-574 are deleted.
Expression of shgdCR3h.Scer\UAS.T:Avic\GFP-rs in eyes, under the control of Scer\GAL4hs.2sev, causes under-rotation of ommatidia. Photoreceptor loss and patterning defects are minimal in these eyes and planar cell polarity defects are not observed. The ommatidial under-rotation is enhanced in flies with a shgk03401/+, shg1/+ or shg2/+ mutant background. The phenotype is suppressed in Scer\GAL4hs.2sev>shgdCR3h.Scer\UAS.T:Avic\GFP-rs; Scer\GAL4hs.2sev>shgScer\UAS.cSa flies.
Coexpression of shgΔβ.Scer\UAS with shgdCR3h.Scer\UAS.T:Avic\GFP-rs, under the control of Scer\GAL4hs.2sev, does not rescue the shgdCR3h.Scer\UAS.T:Avic\GFP-rs ommatidial defects. Likewise, coexpression of shgex.Scer\UAS fails to rescue the ommatidial defects.
When transiently transformed with Scer\GAL4Act5C.PHb into S2 cells, did not promote a cell aggregation phenotype.
Scer\GAL4hs.2sev, shgdCR3h.UAS.sgGFP has abnormal cell polarity phenotype, enhanceable by arm4
Scer\GAL4hs.2sev, shgdCR3h.UAS.sgGFP has abnormal cell polarity phenotype, enhanceable by dgo[+]/dgo380
Scer\GAL4hs.2sev, shgdCR3h.UAS.sgGFP has abnormal cell polarity phenotype, enhanceable by Vangstbm-6/Vang[+]
Scer\GAL4hs.2sev, dgo[+]/dgo380, shgdCR3h.UAS.sgGFP has abnormal cell polarity phenotype, enhanceable by Vangstbm-6/Vang[+]
Scer\GAL4hs.2sev, Vangstbm-6/Vang[+], shgdCR3h.UAS.sgGFP has abnormal cell polarity phenotype, enhanceable by dgo[+]/dgo380
Scer\GAL4hs.2sev, shgdCR3h.UAS.sgGFP has abnormal cell polarity phenotype, enhanceable by Rho172R/Rho1[+]
Scer\GAL4hs.2sev, shgdCR3h.UAS.sgGFP has abnormal cell polarity phenotype, enhanceable by CadNUAS.cIa, Scer\GAL4hs.2sev
Scer\GAL4hs.2sev, shgdCR3h.UAS.sgGFP has abnormal cell polarity phenotype, enhanceable by Rho1RNAi.UAS.cBa, Scer\GAL4hs.2sev
Scer\GAL4hs.2sev, shgdCR3h.UAS.sgGFP has abnormal cell polarity phenotype, non-enhanceable by Df(2L)CadNΔ14/+
Scer\GAL4hs.2sev, shgdCR3h.UAS.sgGFP has abnormal cell polarity phenotype, non-enhanceable by mys1/mys[+]
Scer\GAL4hs.2sev, shgdCR3h.UAS.sgGFP has abnormal cell polarity phenotype, non-enhanceable by fz23/fz[+]
Scer\GAL4hs.2sev, shgdCR3h.UAS.sgGFP has abnormal cell polarity phenotype, non-enhanceable by dsh1/dsh[+]
Scer\GAL4hs.2sev, shgdCR3h.UAS.sgGFP has abnormal cell polarity phenotype, non-enhanceable by stan[+]/stanE59
Scer\GAL4hs.2sev, shgdCR3h.UAS.sgGFP has abnormal cell polarity phenotype, non-enhanceable by nmoP1/nmo[+]
Scer\GAL4hs.2sev, shgdCR3h.UAS.sgGFP has abnormal cell polarity phenotype, non-enhanceable by sca[+]/scaBP1
Scer\GAL4hs.2sev, shgdCR3h.UAS.sgGFP has abnormal cell polarity phenotype, non-enhanceable by rok[+]/Rok2
Scer\GAL4hs.2sev, shgdCR3h.UAS.sgGFP has abnormal cell polarity phenotype, non-enhanceable by arm2
Scer\GAL4hs.2sev, shgdCR3h.UAS.sgGFP has abnormal cell polarity phenotype, non-enhanceable by CadN[+]/CadNM19
Scer\GAL4hs.2sev, shgdCR3h.UAS.sgGFP has abnormal cell polarity phenotype, non-suppressible by Df(2L)CadNΔ14/+
Scer\GAL4hs.2sev, shgdCR3h.UAS.sgGFP has abnormal cell polarity phenotype, non-suppressible by mys1/mys[+]
Scer\GAL4hs.2sev, shgdCR3h.UAS.sgGFP has abnormal cell polarity phenotype, non-suppressible by fz23/fz[+]
Scer\GAL4hs.2sev, shgdCR3h.UAS.sgGFP has abnormal cell polarity phenotype, non-suppressible by dsh1/dsh[+]
Scer\GAL4hs.2sev, shgdCR3h.UAS.sgGFP has abnormal cell polarity phenotype, non-suppressible by stan[+]/stanE59
Scer\GAL4hs.2sev, shgdCR3h.UAS.sgGFP has abnormal cell polarity phenotype, non-suppressible by nmoP1/nmo[+]
Scer\GAL4hs.2sev, shgdCR3h.UAS.sgGFP has abnormal cell polarity phenotype, non-suppressible by sca[+]/scaBP1
Scer\GAL4hs.2sev, shgdCR3h.UAS.sgGFP has abnormal cell polarity phenotype, non-suppressible by rok[+]/Rok2
Scer\GAL4hs.2sev, shgdCR3h.UAS.sgGFP has abnormal cell polarity phenotype, non-suppressible by CadN[+]/CadNM19
Scer\GAL4hs.2sev, shgdCR3h.UAS.sgGFP has ommatidium phenotype, enhanceable by arm4
Scer\GAL4hs.2sev, shgdCR3h.UAS.sgGFP has ommatidium phenotype, enhanceable by dgo[+]/dgo380
Scer\GAL4hs.2sev, shgdCR3h.UAS.sgGFP has ommatidium phenotype, enhanceable by Vangstbm-6/Vang[+]
Scer\GAL4hs.2sev, dgo[+]/dgo380, shgdCR3h.UAS.sgGFP has ommatidium phenotype, enhanceable by Vangstbm-6/Vang[+]
Scer\GAL4hs.2sev, Vangstbm-6/Vang[+], shgdCR3h.UAS.sgGFP has ommatidium phenotype, enhanceable by dgo[+]/dgo380
Scer\GAL4hs.2sev, shgdCR3h.UAS.sgGFP has ommatidium phenotype, enhanceable by Rho172R/Rho1[+]
Scer\GAL4hs.2sev, shgdCR3h.UAS.sgGFP has ommatidium phenotype, enhanceable by CadNUAS.cIa, Scer\GAL4hs.2sev
Scer\GAL4hs.2sev, shgdCR3h.UAS.sgGFP has ommatidium phenotype, enhanceable by Rho1RNAi.UAS.cBa, Scer\GAL4hs.2sev
Scer\GAL4hs.2sev, shgdCR3h.UAS.sgGFP has ommatidium phenotype, non-enhanceable by Df(2L)CadNΔ14/+
Scer\GAL4hs.2sev, shgdCR3h.UAS.sgGFP has ommatidium phenotype, non-enhanceable by mys1/mys[+]
Scer\GAL4hs.2sev, shgdCR3h.UAS.sgGFP has ommatidium phenotype, non-enhanceable by fz23/fz[+]
Scer\GAL4hs.2sev, shgdCR3h.UAS.sgGFP has ommatidium phenotype, non-enhanceable by dsh1/dsh[+]
Scer\GAL4hs.2sev, shgdCR3h.UAS.sgGFP has ommatidium phenotype, non-enhanceable by stan[+]/stanE59
Scer\GAL4hs.2sev, shgdCR3h.UAS.sgGFP has ommatidium phenotype, non-enhanceable by arm2
Scer\GAL4hs.2sev, shgdCR3h.UAS.sgGFP has ommatidium phenotype, non-enhanceable by nmoP1/nmo[+]
Scer\GAL4hs.2sev, shgdCR3h.UAS.sgGFP has ommatidium phenotype, non-enhanceable by sca[+]/scaBP1
Scer\GAL4hs.2sev, shgdCR3h.UAS.sgGFP has ommatidium phenotype, non-enhanceable by rok[+]/Rok2
Scer\GAL4hs.2sev, shgdCR3h.UAS.sgGFP has ommatidium phenotype, non-enhanceable by CadN[+]/CadNM19
Scer\GAL4hs.2sev, shgdCR3h.UAS.sgGFP has ommatidium phenotype, non-suppressible by CadN[+]/CadNM19
Scer\GAL4hs.2sev, shgdCR3h.UAS.sgGFP has ommatidium phenotype, non-suppressible by Df(2L)CadNΔ14/+
Scer\GAL4hs.2sev, shgdCR3h.UAS.sgGFP has ommatidium phenotype, non-suppressible by mys1/mys[+]
Scer\GAL4hs.2sev, shgdCR3h.UAS.sgGFP has ommatidium phenotype, non-suppressible by fz23/fz[+]
Scer\GAL4hs.2sev, shgdCR3h.UAS.sgGFP has ommatidium phenotype, non-suppressible by dsh1/dsh[+]
Scer\GAL4hs.2sev, shgdCR3h.UAS.sgGFP has ommatidium phenotype, non-suppressible by stan[+]/stanE59
Scer\GAL4hs.2sev, shgdCR3h.UAS.sgGFP has ommatidium phenotype, non-suppressible by nmoP1/nmo[+]
Scer\GAL4hs.2sev, shgdCR3h.UAS.sgGFP has ommatidium phenotype, non-suppressible by sca[+]/scaBP1
Scer\GAL4hs.2sev, shgdCR3h.UAS.sgGFP has ommatidium phenotype, non-suppressible by rok[+]/Rok2
The Scer\GAL4hs.2sev>shgdCR3h.Scer\UAS.T:Avic\GFP-rs eye phenotype is enhanced in a arm4 background, both in terms of the under-rotation of ommatidia and in defects associated with ommatidial architecture and adhesion, such as the appearance of gaps between the ommatidia. However, an arm2 background does not enhance the Scer\GAL4hs.2sev>shgdCR3h.Scer\UAS.T:Avic\GFP-rs eye phenotype; arm2 does not affect cell architecture in single mutants.
The under-rotation of ommatidia seen in Scer\GAL4hs.2sev>shgdCR3h.Scer\UAS.T:Avic\GFP-rs eyes is enhanced by coexpression of CadNScer\UAS.cIa.
Coexpression of Rho1dsRNA.Scer\UAS with shgdCR3h.Scer\UAS.T:Avic\GFP-rs, under the control of Scer\GAL4hs.2sev, enhances the under-rotation of ommatidia seen in Scer\GAL4hs.2sev>shgdCR3h.Scer\UAS.T:Avic\GFP-rs eyes. Similarly, expression of shgdCR3h.Scer\UAS.T:Avic\GFP-rs under the control of Scer\GAL4hs.2sev in a Rho172R/+ background, enhances the ommatidial rotation phenotype of shgdCR3h.Scer\UAS.T:Avic\GFP-rs flies.
Neither a CadNM19/+ nor a Df(2L)CadNΔ14/+ background affects the Scer\GAL4hs.2sev>shgdCR3h.Scer\UAS.T:Avic\GFP-rs ommatidial phenotype. Likewise, the following genetic backgrounds do not affect the ommatidial phenotype: mys1/+, fz23/+, dsh1/+, stanE59/+, nmoP1/+, scaBP1/+ and rok2/+.
Both a dgo380/+ and a Vangstbm-6/+ background enhances the ommatidial rotation phenotype of Scer\GAL4hs.2sev>shgdCR3h.Scer\UAS.T:Avic\GFP-rs eyes; a dgo380/+, Vangstbm-6/+ double mutant background further enhances this phenotype.
shgdCR3h.UAS.sgGFP/Scer\GAL4btl.PS partially rescues Df(2R)E2/shg2
The addition of shgdCR3h.Scer\UAS.T:Avic\GFP-rs, driven by Scer\GAL4btl.PS, into shg2/Df(2R)E2 flies partially rescues their tracheal fusion phenotype producing incomplete dorsal trunk fusions.
Carried in a plasmid and co transfected with Scer\GAL4Act5C.PHb into S2 cells.