A single point mutation results in replacement of an aspartic acid for a asparagine at amino acid 222 in orb2 isoform A and at amino acid 91 in isoform B.
Amino acid replacement: D222N.
Amino acid replacement: D91N.
G10406571A
D222N | flw-PA; D91N | flw-PB; D91N | flw-PC; D91N | flw-PD
D222N, D91N
The mutation was reported at position 222 relative to transcript RA and position 91 relative to transcript R-B.
Homozygous female germline clones result in small actin ring canals.
When posterior follicle cells (PFCs) are homozygous mutant for flwFP41 the oocyte nucleus often fails to relocalise and remains at the posterior pole. Oocyte polarity is unaffected when PFCs are wild-type and the anterior or lateral follicle cells are mutant for flwFP41. Some of the cells found in flwFP41 mutant PFC clones have small nuclei compared to controls and occasionally multiple cell layers are present at the posterior. Unlike in wild-type, mitotic PH3 positive PFCs can still be seen after stage 6. This overproliferation phenotype is never observed in clones induced at the lateral side of the epithelium.
flwFP41 has increased cell number | recessive | somatic clone phenotype, enhanceable by Scer\GAL4Act5C.PU/btl::Egfrλ.UAS
flwFP41 has increased cell number | recessive | somatic clone phenotype, enhanceable by Scer\GAL4Act5C.PU/upd1UAS.cZa
flwFP41 has abnormal cell polarity | recessive | somatic clone phenotype, suppressible | partially by Scer\GAL4Act5C.PU/NICN.UAS
flwFP41 has abnormal cell polarity | recessive | somatic clone phenotype, suppressible | partially by Scer\GAL4Act5C.PU/NECN.UAS.cGa
flwFP41 has abnormal cell polarity | recessive | somatic clone phenotype, suppressible | partially by zip[+]/zip1
flwFP41 has abnormal cell polarity | recessive | somatic clone phenotype, suppressible | partially by Rho1E3.10/Rho1[+]
flwFP41 has abnormal cell polarity | recessive | somatic clone phenotype, suppressible | partially by RhoGEF204291/RhoGEF2[+]
flwFP41 has abnormal cell polarity | recessive | somatic clone phenotype, suppressible | partially by Scer\GAL4Act5C.PU/NUAS.cSb
Scer\GAL4Act5C.PU, btl::Egfrλ.UAS, flwFP41 has increased cell number | recessive | somatic clone phenotype
Scer\GAL4Act5C.PU, flwFP41, upd1UAS.cZa has increased cell number | recessive | somatic clone phenotype
flwFP41 has follicle cell | posterior | somatic clone phenotype, enhanceable by Scer\GAL4Act5C.PU/btl::Egfrλ.UAS
flwFP41 has follicle cell | posterior | somatic clone phenotype, enhanceable by Scer\GAL4Act5C.PU/upd1UAS.cZa
flwFP41 has oocyte | somatic clone phenotype, suppressible | partially by zip[+]/zip1
flwFP41 has oocyte | somatic clone phenotype, suppressible | partially by Rho1E3.10/Rho1[+]
flwFP41 has oocyte | somatic clone phenotype, suppressible | partially by RhoGEF204291/RhoGEF2[+]
flwFP41 has oocyte | somatic clone phenotype, suppressible | partially by Scer\GAL4Act5C.PU/NUAS.cSb
flwFP41 has oocyte | somatic clone phenotype, suppressible | partially by Scer\GAL4Act5C.PU/NICN.UAS
flwFP41 has oocyte | somatic clone phenotype, suppressible | partially by Scer\GAL4Act5C.PU/NECN.UAS.cGa
Scer\GAL4Act5C.PU, btl::Egfrλ.UAS, flwFP41 has follicle cell | anterior | somatic clone phenotype
Scer\GAL4Act5C.PU, flwFP41, upd1UAS.cZa has follicle cell | anterior | somatic clone phenotype
Scer\GAL4Act5C.PU, flwFP41, upd1UAS.cZa has follicle cell | lateral | somatic clone phenotype
One copy of zip1 partially suppresses the oocyte polarity defects seen when the posterior follicle cells are mutant for flwFP41.
One copy of Rho1E3.10 partially suppresses the oocyte polarity defects seen when the posterior follicle cells are mutant for flwFP41.
One copy of RhoGEF204291 partially suppresses the oocyte polarity defects seen when the posterior follicle cells are mutant for flwFP41.
Expression of NScer\UAS.cSb under the control of Scer\GAL4Act5C.PU partially suppresses the oocyte polarity defect seen when the posterior follicle cells are mutant for flwFP41.
Expression of NICN.Scer\UAS under the control of Scer\GAL4Act5C.PU partially suppresses the oocyte polarity defect seen when the posterior follicle cells are mutant for flwFP41.
Expression of NECN.Scer\UAS.cGa under the control of Scer\GAL4Act5C.PU partially suppresses the oocyte polarity defect seen when the posterior follicle cells are mutant for flwFP41.
Expression of btl::EgfrScer\UAS.T:λ\cI-DD under the control of Scer\GAL4Act5C.PU in flwFP41 mutant follicle cell clones results in overproliferation in anterior follicle cells but not in lateral follicle cells. The amount of cell overproliferation in posterior follicle cells is increased compared to flwFP41 clones alone.
Expression of upd1Scer\UAS.cZa under the control of Scer\GAL4Act5C.PU in flwFP41 mutant follicle cell clones results in overproliferation in anterior and lateral follicle cells. The amount of cell overproliferation in posterior follicle cells is increased compared to flwFP41 clones alone.
flwFP41 is rescued by flwUAS.Tag:HA/Scer\GAL4e22c
flwFP41 is not rescued by Scer\GAL4VP16.mat.αTub67C/flwUAS.cRa
Expression of flwScer\UAS.cRa under the control of Scer\GAL4tub.PU does not rescue the lethality of flwFP41.
Expression of flwScer\UAS.T:Ivir\HA1 under the control of Scer\GAL4e22c rescues the oocyte polarity defects seen when the posterior follicle cells are mutant for flwFP41.