Amino acid replacement: Y134N.
Nucleotide substitution: T400A.
T27066334A
T400A
Y190N | spz-PA; Y164N | spz-PB; Y117N | spz-PC; Y137N | spz-PD; Y91N | spz-PI; Y108N | spz-PJ; Y154N | spz-PK; Y134N | spz-PL
Y134N
VA1d olfactory receptor neuron axon targeting is normal in mutant flies.
Hemolymph clots from spz2 third instar larvae show normal melanization.
Homozygous females produce dorsalised embryos.
Level of Drs induction of bacterially challenged mutants is lower than in wild type. Pattern of response of CecA1 and CecA2 parallels that of Drs. Dpt and Dro remain fully inducible and pattern of expression of AttA and Def in intermediate. Infection of spz4/spz2 mutants with A.fumigatus causes 3% survival 3 days postinfection, infection with E.coli causes 84% survival 3 days postinfection.
Injection of snkΔne.T:ea into the central region of homozygous embryos causes a dorsalized phenotype.
Perivitelline fluid from Tl and dl donors was capable of restoring polarized gastrulation movements and cuticular elements.
Embryos derived from homozygous females are dorsalised.
spz5e03444, spz2 has abnormal neuroanatomy phenotype, enhanceable by NT141
spz2 has abnormal neuroanatomy phenotype, enhanceable by NT141/spz5e03444
spz2 has increased cell death phenotype, enhanceable by Tlr3/Df(3R)ro80b
NT141, spz2 has abnormal neuroanatomy phenotype, enhanceable by spz5e03444
spz2 has increased cell death phenotype, non-enhanceable by NT141
spz2 has partially lethal phenotype, suppressible by Scer\GAL4elav-C155/Tl10b.UAS.cYa
spz2 has partially lethal phenotype, suppressible by Scer\GAL4elav-C155/Toll-6C1020Y.UAS.Tag:FLAG
spz2 has partially lethal phenotype, suppressible by Toll-7C993Y.UAS.Tag:FLAG/Scer\GAL4elav-C155
spz2/NT141 is an enhancer of abnormal neuroanatomy phenotype of spz5e03444
spz2/spz5e03444 is an enhancer of abnormal neuroanatomy phenotype of NT141
spz2 is an enhancer of abnormal neuroanatomy phenotype of NT141, spz5e03444
spz2 is an enhancer of increased cell death phenotype of Df(3R)ro80b, Tl10b.UAS
spz2 is a non-enhancer of abnormal neuroanatomy phenotype of NT141
spz2 is a non-enhancer of increased cell death phenotype of NT141
spz2 is a non-enhancer of visible phenotype of upd1GMR.PB
spz2 is a non-suppressor of visible phenotype of upd1GMR.PB
spz2 is a non-suppressor of partially lethal - majority die | recessive phenotype of cact7
NT141, spz5e03444, spz2 has abnormal locomotor rhythm phenotype
Df(3L)ED4342/NT141, spz5e03444, spz2 has abnormal locomotor rhythm phenotype
spz5e03444, spz2 has larval intersegmental nerve branch ISNd of A1-7 phenotype, enhanceable by NT141
spz5e03444, spz2 has larval segmental nerve phenotype, enhanceable by NT141
spz5e03444, spz2 has larval transverse nerve phenotype, enhanceable by NT141
spz2 has larval intersegmental nerve branch ISNb of A1-7 phenotype, enhanceable by NT141/spz5e03444
spz2 has larval intersegmental nerve branch ISNd of A1-7 phenotype, enhanceable by NT141/spz5e03444
spz2 has larval segmental nerve branch SNa of A1-7 phenotype, enhanceable by NT141/spz5e03444
spz2 has larval segmental nerve phenotype, enhanceable by NT141/spz5e03444
spz2 has larval transverse nerve phenotype, enhanceable by NT141/spz5e03444
NT141, spz2 has larval intersegmental nerve branch ISNb of A1-7 phenotype, enhanceable by spz5e03444
NT141, spz2 has larval intersegmental nerve branch ISNd of A1-7 phenotype, enhanceable by spz5e03444
NT141, spz2 has larval segmental nerve phenotype, enhanceable by spz5e03444
NT141, spz2 has larval transverse nerve phenotype, enhanceable by spz5e03444
spz5e03444, spz2 has larval intersegmental nerve branch ISNb of A1-7 phenotype, enhanceable by NT141
spz2/NT141 is an enhancer of larval intersegmental nerve branch ISNb of A1-7 phenotype of spz5e03444
spz2/NT141 is an enhancer of larval intersegmental nerve branch ISNd of A1-7 phenotype of spz5e03444
spz2/NT141 is an enhancer of larval segmental nerve branch SNa of A1-7 phenotype of spz5e03444
spz2/NT141 is an enhancer of larval segmental nerve phenotype of spz5e03444
spz2/NT141 is an enhancer of larval transverse nerve phenotype of spz5e03444
spz2/spz5e03444 is an enhancer of larval intersegmental nerve branch ISNb of A1-7 phenotype of NT141
spz2/spz5e03444 is an enhancer of larval intersegmental nerve branch ISNd of A1-7 phenotype of NT141
spz2/spz5e03444 is an enhancer of larval segmental nerve branch SNa of A1-7 phenotype of NT141
spz2/spz5e03444 is an enhancer of larval segmental nerve phenotype of NT141
spz2/spz5e03444 is an enhancer of larval transverse nerve phenotype of NT141
spz2 is an enhancer of larval intersegmental nerve branch ISNb of A1-7 phenotype of NT141, spz5e03444
spz2 is an enhancer of larval intersegmental nerve branch ISNd of A1-7 phenotype of NT141, spz5e03444
spz2 is an enhancer of larval segmental nerve phenotype of NT141, spz5e03444
spz2 is an enhancer of larval transverse nerve phenotype of NT141, spz5e03444
spz2 is a non-enhancer of larval segmental nerve phenotype of NT141
spz2 is a non-enhancer of eye phenotype of upd1GMR.PB
spz2 is a non-suppressor of eye phenotype of upd1GMR.PB
Pan-neuronal expression of Tl10b.Scer\UAS.cYa, under the control of Scer\GAL4elav-C155, suppresses the semi-lethality seen in spz2 mutants.
Pan-neuronal expression of Toll-6C1020Y.Scer\UAS.T:Zzzz\FLAG, under the control of Scer\GAL4elav-C155, suppresses the semi-lethality seen in spz2 mutants.
Pan-neuronal expression of Toll-7C993Y.Scer\UAS.T:Zzzz\FLAG, under the control of Scer\GAL4elav-C155, suppresses the semi-lethality seen in spz2 mutants.
The SNa axonal phenotype of spz2 NT141 double-mutant embryos is epistatic to spz.
Levels of apoptosis increase in the CNS of spz2 and Tlr3/Df(3R)ro80b mutant embryos, indicating that both spz and Tl are required for neuronal survival.
Levels of apoptosis do not increase further in spz2 NT141 double mutants (compared to spz2 mutants).
Whereas homozygous spz2 flies can eclose as adults, the NT141 spz2 double mutants are completely lethal (100% penetrance).
The penetrance of both SNa and ISNb/d targeting defects increases in spz5e03444 NT141 spz2, compared to the double or single mutants. In the triple mutants, misrouting phenotypes can be very dramatic, and there are cases of loss of all ISNb/d motor axons (not seen in single mutants). Misrouting of the transverse nerve (TN) can be very dramatic in triple mutants, although milder effects in this nerve occur with comparable penetrance in all genotypes (~10%). Misroutings of ISN are negligible in single and double mutants, but they increase and can be dramatic in triple-mutant embryos (12.7%).
NT141 spz5e03444 / NT141 Df(3L)Exel6092 double mutant flies display a range of behavioral phenotypes including: inability to estimate the location of a petri dish rim, falling off a petri dish rim, sluggishness, inability to climb, and wobbling.
Perivitelline fluid from embryos laid by Tlrv13 spz4/Tlrv4 spz2 females does not show axis-inducing activity when injected into the perivitelline space of embryos derived from pip1/pip2 females. Perivitelline fluid from embryos laid by eaD3 spz4/ea1 spz2 females does not show axis-inducing activity when injected into the perivitelline space of embryos derived from pip1/pip2 females. Perivitelline fluid from embryos laid by eaD1 spz2/ea4 spz4 females shows axis-inducing activity when injected into the the perivitelline space of embryos derived from pip1/pip2 females.
Double mutant combinations with eaD1 are strongly dorsalizing.
The presence of one copy of spz2 markedly reduces the number of flies with melanin deposits caused by expression of Hsap\CHMP2BIntron5.Scer\UAS under the control of Scer\GAL4GMR.PF.
Microinjection of purified spz2.1 protein into the perivitelline space of syncytial blastoderm stage embryos rescues embryonic phenotype: restores the ventrolateral pattern elements and normalises the dorsal-ventral axis of the recipient embryo.