Nucleotide substitution: G?A.
Amino acid replacement: E324K.
Amino acid replacement: E324K. Nucleotide substitution: G?A.
Amino acid replacement: E?K. Mutation is within the kinase domain.
G8175198A
G?A
E324K | slpr-PA; E324K | slpr-PB; E324K | slpr-PC; E324K | slpr-PD
E324K
E?K
100% of mutant embryos have a severe dorsal open phenotype.
slpr921 displays complete embryonic lethality - dead embryos exhibit a high proportion of severe 'dorsal open' (a hole in the dorsal larval cuticle) phenotypes.
slpr921/Y mutants (lacking zygotic slpr function) are embryonic lethal with a severe dorsal closure phenotype. Mutant embryos derived from homozygous female germline clones (lacking both zygotic and maternal slpr function) show the same cuticle phenotype as zygotically mutant embryos.
Eggs laid by females carrying homozygous follicle cell clones have thin, shortened dorsal appendages.
20% of slpr921/slprBS06 escaper adult females have maxillary palp defects.
slpr921/Y embryos derived from heterozygous females die during embryogenesis with a severe dorsal open phenotype. The concerted elongation of leading edge cells that is seen during dorsal closure initiates correctly in the embryos, but fails shortly afterwards and eventually the cells round up, the dorsal epidermis slackens laterally and the internal organs herniate. A paternal copy of slpr+ can rescue embryos derived from females containing slpr921 homozygous germ-line clones. Mutant embryos derived from females containing homozygous germ-line clones which do not receive a paternal copy of slpr+ die with a severe cuticle phenotype identical to the that of slpr921 zygotic mutants.
slpr921 has lethal - all die during embryonic stage phenotype, suppressible by alphXS-88/alphXS-88
slpr921 has lethal - all die during embryonic stage phenotype, suppressible by alphS-331/alphS-331
slpr921/slpr[+] is a suppressor of visible phenotype of Rac1GMR.PN
slpr921/slpr[+] is a non-suppressor of visible phenotype of Scer\GAL4GMR.PF, egrGS9830
slpr921 has embryo | dorsal closure stage phenotype, suppressible by Scer\GAL4arm.PS/slpr::Tak1STCt.UASp.Tag:HA
slpr921 has embryo | dorsal closure stage phenotype, suppressible by Scer\GAL4arm.PS/slpr::Tak1STK.UASp.Tag:HA
slpr921 has embryonic/first instar larval cuticle | dorsal phenotype, suppressible by alphXS-88/alphXS-88
slpr921 has embryonic/first instar larval cuticle | dorsal phenotype, suppressible by alphS-331/alphS-331
slpr921 has embryo | dorsal closure stage phenotype, suppressible by JraAsp.hs.sev
slpr921 has embryo | dorsal closure stage phenotype, suppressible by pucE69/puc[+]
slpr921 has embryonic/first instar larval cuticle phenotype, suppressible by pucE69/puc[+]
slpr921 has embryonic/first instar larval cuticle phenotype, suppressible by JraAsp.hs.sev
slpr921 has embryo | dorsal closure stage phenotype, non-suppressible by slpr::Tak1SAAATCt.UASp.Tag:HA/Scer\GAL4arm.PS
slpr921 has embryo | dorsal closure stage phenotype, non-suppressible by slpr::Tak1TSK.UASp.Tag:HA/Scer\GAL4arm.PS
slpr921 has embryo | dorsal closure stage phenotype, non-suppressible by Scer\GAL4arm.PS/slpr::Tak1TSAAA.UASp.Tag:HA
slpr921 is an enhancer of mesonotum phenotype of PvrRNAi.UAS, Scer\GAL4pnr-MD237
slpr921 is an enhancer of thorax phenotype of PvrRNAi.UAS, Scer\GAL4pnr-MD237
slpr921/slpr[+] is a non-enhancer of eye phenotype of hepCA.sev.Tag:MYC
slpr921/slpr[+] is a suppressor of eye phenotype of Rac1GMR.PN
slpr921/slpr[+] is a suppressor of ommatidium phenotype of Rac1GMR.PN
slpr921/slpr[+] is a non-suppressor of eye phenotype of hepCA.sev.Tag:MYC
slpr921/slpr[+] is a non-suppressor of eye phenotype of Scer\GAL4GMR.PF, egrGS9830
Expression of slpr::Tak1STCt.Scer\UAS.P\T.T:Ivir\HA1 under the control of Scer\GAL4arm.PS partially rescues the dorsal closure phenotype seen in slpr921 mutant males. Some embryos exhibit head defects.
Expression of slpr::Tak1STK.Scer\UAS.P\T.T:Ivir\HA1 under the control of Scer\GAL4arm.PS partially rescues the dorsal closure phenotype seen in slpr921 mutant males. Some embryos exhibit head defects.
Expression of slpr::Tak1SAAATCt.Scer\UAS.P\T.T:Ivir\HA1 under the control of Scer\GAL4arm.PS does not rescue the dorsal closure phenotype seen in slpr921 mutant males. Some embryos exhibit head defects.
Expression of slpr::Tak1TSK.Scer\UAS.P\T.T:Ivir\HA1 under the control of Scer\GAL4arm.PS does not rescue the dorsal closure phenotype seen in slpr921 mutant males. Some embryos exhibit head defects.
Expression of slpr::Tak1TSAAA.Scer\UAS.P\T.T:Ivir\HA1 under the control of Scer\GAL4arm.PS does not rescue the dorsal closure phenotype seen in slpr921 mutant males. Some embryos exhibit head defects.
Expression of Tak1Ct.Scer\UAS.P\T.T:Ivir\HA1 under the control of Scer\GAL4arm.PS does not rescue the dorsal closure phenotype seen in slpr921 mutant males. Some embryos exhibit head defects.
The eye ablation phenotype seen in adults expressing egrGS9830 under the control of Scer\GAL4GMR.PF is not suppressed by slpr921/+.
The severe dorsal open phenotype of slpr921/Y embryos is significantly rescued by expression of JraAsp.hs.sev (using a 30 minute heat shock several hours before the beginning of dorsal closure) and is also significantly rescued by pucE69/+.
slpr921 is rescued by Scer\GAL4arm.PS/slprUASp.Tag:HA
slpr921 is rescued by Scer\GAL4arm.PS/slprSKLC.UASp.Tag:HA
slpr921 is rescued by slprUASp.cPa/Scer\GAL4arm.PS
slpr921 is rescued by slprUASp.cPa/Scer\GAL4arm.PS
slpr921 is partially rescued by Scer\GAL4arm.PS/slprUASp.Tag:HA
slpr921 is partially rescued by Scer\GAL4arm.PS/slprSKLC.UASp.Tag:HA
slpr921 is partially rescued by slprΔSH3.UASp.Tag:HA/Scer\GAL4arm.PS
slpr921 is not rescued by slprAAA.UASp.Tag:HA/Scer\GAL4arm.PS
slpr921 is not rescued by slprAAA.UASp.Tag:HA/Scer\GAL4arm.PS
slpr921 is not rescued by slprTAA.UASp.Tag:HA/Scer\GAL4arm.PS
slpr921 is not rescued by slprASA.UASp.Tag:HA/Scer\GAL4arm.PS
slpr921 is not rescued by slprAAT.UASp.Tag:HA/Scer\GAL4arm.PS
slpr921 is not rescued by slprSKLC.AAA.UASp.Tag:HA/Scer\GAL4arm.PS
slpr921 is not rescued by slprSH3.UASp.Tag:HA/Scer\GAL4arm.PS
slpr921 is not rescued by Scer\GAL4arm.PS/slprCterm.UASp.Tag:HA
slpr921 is not rescued by Scer\GAL4arm.PS/slprAVA.UASp.Tag:HA
Expression of slprScer\UAS.P\T.T:Ivir\HA1 under the control of Scer\GAL4arm.PS rescues the dorsal closure phenotype seen in slpr921 mutant males. Some embryos exhibit head defects.
Expression of slprSKLC.Scer\UAS.P\T.T:Ivir\HA1 under the control of Scer\GAL4arm.PS partially rescues the dorsal closure phenotype seen in slpr921 mutant males. Some embryos exhibit head defects.
Expression of slprAAA.Scer\UAS.P\T.T:Ivir\HA1 under the control of Scer\GAL4arm.PS does not rescue the dorsal closure phenotype seen in slpr921 mutant males. Some embryos exhibit head defects.
The lethality of slpr921 mutants is completely rescued by expression of slprScer\UAS.P\T.cPa under the control of Scer\GAL4arm.PS.
The lethality of slpr921 mutants is partially rescued by expression of slprScer\UAS.P\T.T:Ivir\HA1 or slprSKLC.Scer\UAS.P\T.T:Ivir\HA1 under the control of Scer\GAL4arm.PS.
The lethality of slpr921 mutants is not rescued by expression of slprAAA.Scer\UAS.P\T.T:Ivir\HA1, slprTAA.Scer\UAS.P\T.T:Ivir\HA1, slprASA.Scer\UAS.P\T.T:Ivir\HA1, slprSKLC.AAA.Scer\UAS.P\T.T:Ivir\HA1, slprSH3.Scer\UAS.P\T.T:Ivir\HA1, slprAVA.Scer\UAS.P\T.T:Ivir\HA1, slprCterm.Scer\UAS.P\T.T:Ivir\HA1 or slprΔSH3.Scer\UAS.P\T.T:Ivir\HA1 under the control of Scer\GAL4arm.PS.
Expression of slprAAT.Scer\UAS.P\T.T:Ivir\HA1 under the control of Scer\GAL4arm.PS in slpr921 mutants results in the recovery of a few rescued adults and many more rescued animals are observed as pharate adults.
Expression of slprSH3.Scer\UAS.P\T.T:Ivir\HA1, slprSKLC.AAA.Scer\UAS.P\T.T:Ivir\HA1 or slprCterm.Scer\UAS.P\T.T:Ivir\HA1 under the control of Scer\GAL4arm.PS fails to rescue the severe dorsal open phenotype of slpr921 embryos.
Expression of slprSKLC.Scer\UAS.P\T.T:Ivir\HA1 under the control of Scer\GAL4arm.PS significantly rescues the severe dorsal open phenotype of slpr921 embryos (the penetrance of the phenotype is reduced from 100% to approximately 30%).
Expression of slprΔSH3.Scer\UAS.P\T.T:Ivir\HA1 under the control of Scer\GAL4arm.PS significantly rescues the severe dorsal open phenotype of slpr921 embryos (the penetrance of the phenotype is reduced from 100% to approximately 20%).
Expression of slprScer\UAS.P\T.T:Ivir\HA1 under the control of Scer\GAL4arm.PS significantly rescues the severe dorsal open phenotype of slpr921 embryos (the penetrance of the phenotype is reduced from 100% to approximately 10%).