Amino acid replacement: W491term.
G4066546A
W491term | wit-PA; W491term | wit-PB
W491term
G to A nucleotide change at the second or third position of the Trp codon leads to a nonsense mutation. (exact site of mutation unspecified). Site of nucleotide substitution in mutant inferred by FlyBase based on reported amino acid change.
witHA3/witA12 has abnormal neuroanatomy | third instar larval stage phenotype, suppressible | partially by Scer\GAL4BG380/trioUAS.cBa
witB11/witHA3 has abnormal neuroanatomy phenotype, suppressible by tkv::wittkv-EC.wit-IC.Ubi-p63E/tkv::witwit-EC.tkv-IC.Ubi-p63E
witHA3/witA12 has abnormal size | third instar larval stage phenotype, non-suppressible by Scer\GAL4BG380/Rac1V12.UAS
witHA3/witA12 has abnormal neuroanatomy | third instar larval stage phenotype, non-suppressible by Scer\GAL4BG380/Rac1V12.UAS
witHA3/witA12 has abnormal neurophysiology | third instar larval stage phenotype, non-suppressible by Scer\GAL4BG380/Rac1UAS.cLa
witHA3/witA12 has abnormal size | third instar larval stage phenotype, non-suppressible by Scer\GAL4BG380/Rac1UAS.Tag:MYC
witHA3/witA12 has abnormal neuroanatomy | third instar larval stage phenotype, non-suppressible by Scer\GAL4BG380/Rac1UAS.Tag:MYC
witHA3/witA12 is a suppressor of abnormal neurophysiology | third instar larval stage phenotype of Rac1UAS.cLa, Scer\GAL4BG380
witHA3/witA12 is a suppressor of abnormal size | third instar larval stage phenotype of Rac1UAS.Tag:MYC, Scer\GAL4BG380
witHA3/witA12 is a suppressor of abnormal neuroanatomy | third instar larval stage phenotype of Rac1UAS.Tag:MYC, Scer\GAL4BG380
witHA3/witA12 is a non-suppressor of abnormal size | third instar larval stage phenotype of Rac1V12.UAS, Scer\GAL4BG380
witHA3/witA12 is a non-suppressor of abnormal neuroanatomy | third instar larval stage phenotype of Rac1V12.UAS, Scer\GAL4BG380
Mad1, witHA3/wit[+] has abnormal neuroanatomy | dominant phenotype
tkv8, witHA3/wit[+] has abnormal neuroanatomy | dominant phenotype
Mad[+]/Mad1, witHA3 has abnormal neuroanatomy phenotype
Med[+]/MedC246, witHA3 has abnormal neuroanatomy phenotype
sax4/sax[+], witHA3 has abnormal neuroanatomy phenotype
tkv8/tkv[+], witHA3 has abnormal neuroanatomy phenotype
MedC246, witHA3/wit[+] has abnormal neuroanatomy | dominant phenotype
sax4, witHA3/wit[+] has abnormal neuroanatomy | dominant phenotype
witHA3/witA12 has embryonic/larval neuromuscular junction | third instar larval stage phenotype, suppressible | partially by Scer\GAL4BG380/trioUAS.cBa
witHA3/witA12 has NMJ bouton | third instar larval stage phenotype, suppressible | partially by Scer\GAL4BG380/trioUAS.cBa
witB11/witHA3 has neuromuscular junction phenotype, suppressible by tkv::wittkv-EC.wit-IC.Ubi-p63E/tkv::witwit-EC.tkv-IC.Ubi-p63E
witHA3/witA12 has embryonic/larval neuromuscular junction | third instar larval stage phenotype, non-suppressible by Scer\GAL4BG380/Rac1UAS.Tag:MYC
witHA3/witA12 has NMJ bouton | third instar larval stage phenotype, non-suppressible by Scer\GAL4BG380/Rac1UAS.Tag:MYC
witHA3/witA12 has embryonic/larval neuromuscular junction | third instar larval stage phenotype, non-suppressible by Scer\GAL4BG380/Rac1V12.UAS
witHA3/witA12 has NMJ bouton | third instar larval stage phenotype, non-suppressible by Scer\GAL4BG380/Rac1V12.UAS
witHA3/witA12 is a suppressor of embryonic/larval neuromuscular junction | third instar larval stage phenotype of Rac1UAS.Tag:MYC, Scer\GAL4BG380
witHA3/witA12 is a suppressor of NMJ bouton | third instar larval stage phenotype of Rac1UAS.Tag:MYC, Scer\GAL4BG380
witHA3/witA12 is a non-suppressor of embryonic/larval neuromuscular junction | third instar larval stage phenotype of Rac1V12.UAS, Scer\GAL4BG380
witHA3/witA12 is a non-suppressor of NMJ bouton | third instar larval stage phenotype of Rac1V12.UAS, Scer\GAL4BG380
tkv8, witHA3/wit[+] has neuromuscular junction phenotype
Mad1, witHA3 has neuromuscular junction phenotype
MedC246, witHA3 has neuromuscular junction phenotype
Mad1, witHA3/wit[+] has neuromuscular junction phenotype
sax4, witHA3 has neuromuscular junction phenotype
tkv8, witHA3 has neuromuscular junction phenotype
MedC246, witHA3/wit[+] has neuromuscular junction phenotype
sax4, witHA3/wit[+] has neuromuscular junction phenotype
Expression of witA12/witHA3 suppresses the larval neuromuscular junction overgrowth and bouton number phenotypes seen when Rac1Scer\UAS.T:Hsap\MYC is expressed in motor neurons under the control of Scer\GAL4BG380, instead producing a reduction in bouton number similar to the phenotype seen in witA12/witHA3 third instar larvae.
Expression of witA12/witHA3 fails to suppress the larval neuromuscular junction overgrowth and bouton number phenotypes seen when Rac1V12.Scer\UAS is expressed in motor neurons under the control of Scer\GAL4BG380.
witA12/witHA3 suppresses the increase in evoked excitatory junctional potential (EJPs) and quantal content seen when Rac1Scer\UAS.cLa is expressed in motor neurons under the control of Scer\GAL4BG380, with third instar larvae instead displaying the reduction in neurotransmitter release phenotype seen in witA12/witHA3 mutants.
Expression of trioScer\UAS.cBa in motor neurons under the control of Scer\GAL4BG380 partially suppresses the reduced bouton number phenotype seen in witA12/witHA3 larval neuromuscular junctions.
The number of synaptic boutons/muscle surface area at muscle 6/7 in MedC246/witHA3 double heterozygotes is 91.3 +/- 2.7 % of wild type. The number of synaptic boutons/muscle surface area at muscle 6/7 in Mad1/witHA3 double heterozygotes is 95.9 +/- 2.2 % of wild type. The number of synaptic boutons/muscle surface area at muscle 6/7 in sax4/witHA3 double heterozygotes is 85.2 +/- 3.6 % of wild type. The number of synaptic boutons/muscle surface area at muscle 6/7 in tkv8/witHA3 double heterozygotes is 88.8 +/- 2.4 % of wild type. Co-expression of tkv::witwit-EC.tkv-IC.Ubi-p63E and tkv::wittkv-EC.wit-IC.Ubi-p63E rescues the neuromuscular junction size in witHA3/witB11 animals.