Amino acid replacement: Q116term.
Nucleotide substitution: C?T.
C8425654T
C?T
Q116term | Cbl-PA; Q116term | Cbl-PB
Q116term
wing vein | ectopic, with CblS.Hsp83
CblF165 heterozygote adult females do not display any defects in the number of cytoophidia (CTPsyn filaments) in the egg chambers (when kept at 29[o]C) or in DNA replication (measured by BrdU incorporation) in stage 9 egg chambers compared to respective controls.
Majority of follicle cells in CblF165 homozygous somatic clones display significantly reduced number or complete absence of cytoophidia (CTPsyn filaments) in stage 9 and 10 egg chambers compared to controls. However, the cytoophidia are maintained as normal in CblF165 mutant clones in younger egg chambers - before stage 6 and still in the mitotic stages of their development and the macro-cytoophidia in germline clone cells are also not affected. Decrease in cytoophidia numbers is also observed CblF165/CblF165 somatic clones in salivary glands of third instar larvae.
Follicle cells in CblBB28 homozygous mutant somatic clones display endocycle defects in stage 9 and 10A (but not 10B) egg chambers: the number of cells in S-phase (BrdU positive) is significantly decreased compared to controls.
CblF165 homozygous third instar larvae are of a normal size but their salivary glands are smaller and display endocycle defects (measured by BrdU incorporation) compared to wild-type. However, average nuclear size of cells in CblF165 somatic clones (both in salivary glands in third instar larvae and follicle cells in adult females) is not significantly changed compared to twin clone controls.
CblF165 heterozyous ovaries do not exhibit any abnormalities.
CblF165 mutant cells are preferentially located at the front of the cluster during border cell posterior and dorsal migration in mosaic border cell clusters consisting of both wild-type and mutant cells.
Border follicle cells are correctly specified in somatic clones of CblF165 homozygous cells but their migration is severely defective and sometimes fails completely. However, around 50% of migrating clusters do eventually reach the oocyte.
Females containing somatic clones of CblF165 induced in the follicle cells produce dorsalised embryos and egg shells; in some cases egg shells with two dorsal appendages positioned further apart than normal are produced (characteristic of a weakly dorsalised phenotype), and partially or completely dorsalised embryos are produced as evidenced by the loss of ventrally derived structures. Only clones at ventral positions within the follicle cell epithelium result in a dorsalised embryo phenotype, such as a missing head skeleton, reduction of ventral structures (such as denticle belts) in the thoracic and anterior abdominal segments and a twisted embryo. Clones that are confined to the dorsal half of the follicle epithelium do not produce a visible embryonic mutant phenotype. When dorsolateral follicle cells are homozygous for CblF165, dorsal appendages are shifted to more lateral positions than normal. When more lateral cells (adjacent to the dorsal appendages) are homozygous for CblF165, extra or wider dorsal appendages are produced. Somatic clones of CblF165 induced in the wing result in an extra vein phenotype. Embryos lacking both maternal and zygotic Cbl function (derived from homozygous germline clones) have a distinct head defect. Zygotic Cbl function is able to rescue the maternal lack of Cbl function, resulting in normal embryos that hatch.
CblF165 has abnormal endomitotic cell cycle | somatic clone | adult stage phenotype, suppressible by CtpsUAS.Tag:FLAG/Scer\GAL4hs.PU
CblF165 has abnormal endomitotic cell cycle | somatic clone | adult stage phenotype, non-suppressible by Scer\GAL4hs.PU/CtpsC399G.UAS.Tag:FLAG
CblF165 is an enhancer of visible phenotype of Scer\GAL4GMR.PF, cindrRNAi.PC.PD.UAS
CblF165/Cbl[+] is an enhancer of abnormal endomitotic cell cycle | adult stage phenotype of CtpsGD4740, Scer\GAL4CY2
CblF165 is a non-enhancer of visible phenotype of CanBGMR.PS, Pp2B-14Dact.GMR
CblF165 is a suppressor of increased cell death phenotype of Rbf120a
CblF165/Cbl[+] is a suppressor | partially of abnormal endomitotic cell cycle phenotype of Fmr1Δ50M/Fmr13
CblF165/Cbl[+] is a suppressor of visible phenotype of Scer\GAL4ap-md544, Socs36EUASp.cCa
CblF165 is a non-suppressor of visible phenotype of CanBGMR.PS, Pp2B-14Dact.GMR
CblF165 has border follicle cell | somatic clone phenotype, enhanceable by EgfrUAS.cBa/Scer\GAL4slbo.2.6
CblF165 has border follicle cell | somatic clone phenotype, enhanceable by Scer\GAL4slbo.2.6/PvrUAS.cDa
CblF165 has border follicle cell | somatic clone phenotype, enhanceable by spri6G1/spri6G1
CblF165 has follicle cell | somatic clone | adult stage phenotype, suppressible by CtpsUAS.Tag:FLAG/Scer\GAL4hs.PU
CblF165 has cytoophidium | female | somatic clone | adult stage phenotype, suppressible by Scer\GAL4hs.PU/CtpsC399G.UAS.Tag:FLAG
CblF165 has follicle cell | somatic clone | adult stage phenotype, suppressible by Scer\GAL4hs.PU/CtpsC399G.UAS.Tag:FLAG
CblF165 has border follicle cell | somatic clone phenotype, suppressible by grkunspecified/grk[+]
CblF165 has cytoophidium | female | somatic clone | adult stage phenotype, non-suppressible by CtpsUAS.Tag:FLAG/Scer\GAL4hs.PU
CblF165 has follicle cell | somatic clone | adult stage phenotype, non-suppressible by CtpsUAS.Tag:FLAG/Scer\GAL4hs.PU
CblF165 has follicle cell | somatic clone | adult stage phenotype, non-suppressible by Scer\GAL4hs.PU/CtpsC399G.UAS.Tag:FLAG
CblF165 is an enhancer of eye phenotype of Scer\GAL4GMR.PF, cindrRNAi.PC.PD.UAS
CblF165/Cbl[+] is an enhancer of follicle cell | adult stage phenotype of CtpsGD4740, Scer\GAL4CY2
CblF165/Cbl[+] is an enhancer of nucleus | adult stage phenotype of CtpsGD4740, Scer\GAL4CY2
CblF165/Cbl[+] is an enhancer of interommatidial precursor cell phenotype of Scer\GAL4GMR.PF, cindrRNAi.PC.PD.UAS, cindrRNAi.UAS
CblF165/Cbl[+] is an enhancer of primary pigment cell phenotype of Scer\GAL4GMR.PF, cindrRNAi.PC.PD.UAS, cindrRNAi.UAS
CblF165/Cbl[+] is an enhancer of cone cell phenotype of Scer\GAL4GMR.PF, cindrRNAi.PC.PD.UAS, cindrRNAi.UAS
CblF165 is a non-enhancer of eye phenotype of CanBGMR.PS, Pp2B-14Dact.GMR
CblF165/Cbl[+] is a suppressor of nurse cell phenotype of Fmr13
CblF165/Cbl[+] is a suppressor | partially of nurse cell phenotype of Fmr1Δ50M/Fmr13
CblF165/Cbl[+] is a suppressor | partially of nurse cell | increased number phenotype of Fmr13
CblF165 is a suppressor of eye photoreceptor cell | somatic clone phenotype of mopT612
CblF165/Cbl[+] is a suppressor | partially of anterior crossvein phenotype of Scer\GAL4en-e16E, Socs36EUASp.cCa
CblF165/Cbl[+] is a suppressor | partially of wing phenotype of Scer\GAL4en-e16E, Socs36EUASp.cCa
CblF165/Cbl[+] is a non-suppressor of nurse cell | increased number phenotype of Fmr1Δ50M/Fmr13
CblF165 is a non-suppressor of eye phenotype of CanBGMR.PS, Pp2B-14Dact.GMR
CblF165, CtpsGD4740, Scer\GAL4CY2 has egg phenotype
CblF165, Prosβ61 has egg chamber phenotype
CblF165, Prosβ61 has cytoophidium | female | adult stage phenotype
The number of cytoophidia (CTPsyn filaments) in the egg chambers of adult Prosβ61,CblF165 double heterozygote females is significantly reduced compared to either Prosβ61 or CblF165 single heterozygotes.
About a fifth of eggs laid by CblF165 heterozygous females expressing CTPsynGD4740 under the control of Scer\GAL4CY2 has a defective collapsed phenotype that is not observed in eggs laid by CblF165/+ flies.
The loss of cytoophidia (CTPsyn filaments) observed in somatic clones of CblF165 homozygous mutant follicle cells is not suppressed by expression of CTPsynScer\UAS.T:Zzzz\FLAG under the control of Scer\GAL4hs.PU in the clones, although the CTPsynScer\UAS.T:Zzzz\FLAG protein can be incorporated in the cytoophidia filament structure together with endogenous CTPsyn protein in wild-type cells.
The loss of cytoophidia observed in somatic clones of CblF165 homozygous mutant follicle cells is suppressed by expression of CTPsynC399G.Scer\UAS.T:Zzzz\FLAG under the control of Scer\GAL4hs.PU in the clones, although the CTPsynC399G.Scer\UAS.T:Zzzz\FLAG protein cannot be incorporated in the cytoophidia filament structure together with endogenous CTPsyn protein in wild-type cells.
The endocycle defects (decrease in DNA replication measured by BrdU incorporation) seen in somatic clones of CblF165 homozygous mutant follicle cells is partially suppressed by expression of CTPsynScer\UAS.T:Zzzz\FLAG but not suppressed by expression of CTPsynC399G.Scer\UAS.T:Zzzz\FLAG under the control of Scer\GAL4hs.PU in the clones.
The decrease in percentage of follicle cells undergoing DNA replication (measured by BrdU incorporation) observed in stage 9 egg chambers as well as the decreased follicle cell nuclear size in stage 10A egg chamber expressing CTPsynGD4740 under the control of Scer\GAL4CY2 is further decreased by combination with CblF165 in heterozygous state.
CblF165/+ enhances the mis-patterning of interommatidial precursor cells, primary primary pigment cells and cone cells caused by co-expression of cindrdsRNA.Scer\UAS and cindrdsRNA.PC.PD.Scer\UAS under the control of Scer\GAL4GMR.PF.
CblF165 is a dominant suppressor of the germ cell proliferation defects in Fmr13 and Fmr13/Fmr1Δ50M mutant ovaries.
The fewer germ cell phenotype in Fmr13 mutant ovaries is completely suppressed by CblF165/+, while the supernumerary germ cell phenotype is suppressed only partially.
The fewer germ cell phenotype in Fmr13/Fmr1Δ50M ovaries is largely suppressed by CblF165/+, while the supernumerary germ cell phenotype is not suppressed at all.
Defective migration of border follicle cells in CblF165 homozygous somatic clones is suppressed by grkunspecified/+ but enhanced by EgfrScer\UAS.cBa or PvrScer\UAS.cDa with Scer\GAL4slbo.2.6.
spri6G1/spri6G1 also enhances the migration defects seen in border follicle cells in CblF165 homozygous somatic clones. I these animals, border follicle cell clusters rarely reach the oocyte.
Expression of Socs36EScer\UAS.P\T.cCa under the control of Scer\GAL4en-e16E in a CblF165/+ background results in a partial rescue of the Socs36EScer\UAS.P\T.cCa anterior crossvein phenotype, with a reduction in penetrance from 95 to 48%. The penetrance of the outstretched wing phenotype of Scer\GAL4ap-md544>Socs36EScer\UAS.P\T.cCa flies is reduced from 82 to 54% when flies have a CblF165/+ background.
CblF165 is rescued by CblL.Hsp83
CblF165 is rescued by CblS.Hsp83
CblF165 is rescued by CblL.mPR.Hsp83
CblF165 is rescued by CblS.Hsp83
CblF165 is rescued by CblS.αTub84B.PJ
CblF165 is rescued by CblL.αTub84B.PJ
CblF165 is partially rescued by CblS.Hsp83
CblF165 is partially rescued by CblL.mPR.Hsp83
CblF165 is not rescued by CblS.Δ70Z.Hsp83
CblF165 is not rescued by CblL.Δ70Z.Hsp83
CblF165 is not rescued by CblL.Δ70Z.Hsp83
CblF165 is not rescued by CblRing.S.αTub84B
Expression of either CblL.mPR.Hsp83 or CblS.Hsp83 in the follicle cell somatic clones homozygous for CblF165 partially rescues the loss of cytoophidia in stage 9 egg chambers - the proportion of cells completely lacking cytoophidia is significantly decreased.
Expression of either CblS.Δ70Z.Hsp83 or CblL.Δ70Z.Hsp83 in the follicle cell somatic clones homozygous for CblF165 does not rescues the loss of cytoophidia (CTPsyn filaments) in stage 9 egg chambers.
Expression of CblL.mPR.Hsp83 rescues the lethality of CblF165, and 75-80% of animals develop to adults.
Expression of CblL.Δ70Z.Hsp83 fails to rescue CblF165.
Lethality due to CblF165/CblF165 is rescued by CblS.αTub84B.PJ or CblL.αTub84B.PJ as is the border cell migration defect seen in CblF165 homozygous somatic clones. In contrast, CblC369A.SαTub84B.PJ fails to rescue either of these phenotypes.