Amino acid replacement: R104W.
C21114900T
R104W | Rab11-PA; R104W | Rab11-PB
R104W
Site of nucleotide substitution in mutant inferred by FlyBase based on reported amino acid change.
lethal (with Df(3R)e-R1)
Rab1193Bi mutants exhibit synaptic overgrowth with excess satellite boutons on neuromuscular junction 4.
Homozygotes show a small increase in the total number of multi-nucleate spermatids compared to controls.
Testes from Rab1193Bi homozygous larvae, or larvae in which Rab1193Bi is transheterozygous with any of Rab11EP3017, Rab11ETo11 or Rab11ETo3, have spermatids composed of an abnormally large Nebenkern associated with multiple nuclei.
Mid and late telophases in Rab1193Bi/Rab11ETo11 spermatocytes display contractile rings that are not fully constricted or poorly constricted and broken into irregular pieces. Defective central spindles are seen in 80% of these cases. In those spermatocytes that failed to complete cytokinesis, the furrow ingresses to a limited extent and then regresses, coincident with disassembly of the central spindle.
48% of telophases in Rab1193Bi/Rab11ETo11 spermatocytes display abnormal localization of Golgi-derived vesicle-like structures.
Rab1193Bi/Rab11ETo11 testes show disorganized acroblasts in both early and (particularly) elongating spermatids.
Rab1193Bi/Rab11ETo11 brains do not exhibit polyploid mitoses.
Rab1193Bi/+ flies show no eye phenotype.
Rab11ex1/Rab1193Bi transheterozygotes are mostly lethal but a few survive to adulthood.
The posterior abdomens of Rab11ex1/Rab1193Bi flies have empty sockets that are missing microchaetae. Additionally, posterior scutellar bristles are shortened in these mutants. Rab1193Bi homozygotes also show microchaetae loss, although this is less extensive.
The synapse of muscle 6/7 shows an increase in boutons by about 60% in Rab11ex1/Rab1193Bi mutants compared to controls. The boutons of Rab11ex1/Rab1193Bi mutants are often clustered resulting in a 'bunch of grapes' morphology instead of the wild-type 'beads-on-a-string' morphology. The aberrant morphology may reflect increased branching (by 2.6 fold) of Rab11ex1/Rab1193Bi boutons.
8% of Rab1193Bi/Rab11j2D1-derived embryos exhibit disrupted nuclear morphology in premigration and early cortical divisions. During the late cortical divisions, when the nuclei are more densely packed, 65% of embryos exhibit severely disrupted nuclear morphology. In Rab1193Bi/Rab11j2D1-derived nuclear cycle 12 embryos, actin cap formation occurs normally. As the embryos progress into prophase, the actin caps are dismantled as the actin re-organises into furrows encompassing each prophase nucleus and its developing spindle. In Rab1193Bi/Rab11j2D1-derived embryos, the hexagonal furrow network is riddled with gaps, present at prophase during the initial stages of furrow formation. Similar defects are observed during cellularisation at nuclear cycle 14.
Rab1193Bi has some die during embryonic stage phenotype, enhanceable by Nin1
Rab1193Bi/Rab11j2D1 has majority die during embryonic stage phenotype, enhanceable by Nin1
Rab1193Bi has abnormal meiotic cell cycle | male phenotype, enhanceable by bru[+]/brunZ3358
Rab1193Bi has abnormal cytokinesis | male phenotype, enhanceable by bru[+]/brunZ3358
Rab1193Bi/Rab11[+] is an enhancer of abnormal neuroanatomy | larval stage phenotype of Acsl05847/Acsl8
Rab1193Bi/Rab1193Bi is an enhancer of abnormal neuroanatomy | larval stage phenotype of Acsl05847/Acsl8
Rab1193Bi/Rab11[+] is an enhancer of visible phenotype of Scer\GAL4GMR.PF, bchsEP2299
Rab1193Bi/Rab11ETo11 is a non-enhancer of abnormal cytokinesis | male phenotype of fwdZ0453/fwd3
Rab1193Bi/Rab11ETo11 is a non-enhancer of abnormal cytokinesis | male phenotype of vibEP513
Rab1193Bi/Rab11ETo11 is a non-suppressor of abnormal cytokinesis | male phenotype of vibEP513
Rab1193Bi/Rab11ETo11 is a non-suppressor of abnormal cytokinesis | male phenotype of fwdZ0453/fwd3
Madk00237, Rab1193Bi has abnormal neuroanatomy | larval stage phenotype
Acsl05847/AcslKO, Rab1193Bi/Rab11[+] has lethal - all die before end of larval stage phenotype
Rab1193Bi, brunZ3358 has lethal | larval stage phenotype
Rab1193Bi/Rab11ETo3, brunZ3358 has lethal | larval stage phenotype
Rab1193Bi/Rab11ETo11, fwdZ0453/fwd3 has abnormal cytokinesis | male phenotype
Rab1193Bi/Rab11ETo11, vibEP513 has abnormal cytokinesis | male phenotype
Rab1193Bi has microchaeta phenotype, suppressible by bchs58/bchs58
Rab1193Bi has microchaeta phenotype, suppressible | partially by bchs58/bchs[+]
Rab1193Bi has microchaeta phenotype, suppressible | partially by bchs8K/bchs[+]
Rab1193Bi/Rab11ex1 has microchaeta phenotype, suppressible | partially by bchs17/bchs[+]
Rab1193Bi/Rab11ex1 has microchaeta phenotype, suppressible | partially by Df(2L)cl7/+
Rab1193Bi/Rab11ex1 has microchaeta phenotype, suppressible by Df(2L)cl7/bchs17
Rab1193Bi/Rab11ex1 has microchaeta phenotype, suppressible by bchs17/bchs12
Rab1193Bi/Rab11ex1 has posterior scutellar bristle phenotype, suppressible | partially by bchs17/bchs[+]
Rab1193Bi/Rab11ex1 has posterior scutellar bristle phenotype, suppressible | partially by Df(2L)cl7/+
Rab1193Bi/Rab11[+] is an enhancer of neuromuscular junction phenotype of Acsl05847/Acsl8
Rab1193Bi/Rab1193Bi is an enhancer of NMJ bouton | increased number phenotype of Acsl05847/Acsl8
Rab1193Bi/Rab11[+] is an enhancer of eye phenotype of Scer\GAL4GMR.PF, bchsEP2299
Rab1193Bi/Rab11ETo11 is a non-enhancer of spermatid phenotype of fwdZ0453/fwd3
Rab1193Bi/Rab11ETo11 is a non-enhancer of spermatid phenotype of vibEP513
Rab1193Bi/Rab11ETo11 is a non-suppressor of spermatid phenotype of vibEP513
Rab1193Bi/Rab11ETo11 is a non-suppressor of spermatid phenotype of fwdZ0453/fwd3
Madk00237, Rab1193Bi has NMJ bouton phenotype
Madk00237, Rab1193Bi has neuromuscular junction phenotype
Rab1193Bi/Rab11ETo11, fwdZ0453/fwd3 has spermatid phenotype
Rab1193Bi/Rab11ETo11, vibEP513 has spermatid phenotype
Rab1193Bi, Madk00237 double mutants exhibit undergrown synapses with few boutons on neuromuscular junction 4 that are indistinguishable from Madk00237 single mutants.
Acsl05847/AcslKO Rab1193Bi/+ animals do not survive to wandering third instar larvae.
Rab1193Bi/+ and, to a greater extent, Rab1193Bi/Rab1193Bi significantly increases neuromuscular junction overgrowth of Acsl05847/Acsl8 mutants.
Flies homozygous for both bruZ3358 and Rab1193Bi die in early larval stages at 25[o]C, as do flies homozygous for bruZ3358 and transheterozygous for Rab1193Bi/Rab11ETo3.
bruZ3358/+ males also homozygous for Rab1193Bi display a four-fold increase in the total number of multi-nucleate spermatids compared with males homozygous for Rab1193Bi alone.
Rab1193Bi/Rab11ETo11, fwd3/fwdZ0453 spermatids are multinucleated at a similar frequency to fwd3/fwdZ0453 spermatids.
Rab1193Bi/Rab11ETo11, vibEP513 spermatids are multinucleated at a similar frequency to vibEP513 spermatids.
Rab1193Bi heterozygotes act as dominant enhancers of the Scer\GAL4GMR.PF>bchsEP2299 eye phenotype, resulting in adults with severely reduced eyes.
The viability of Rab11ex1/Rab1193Bi is increased when flies are also mutant for either Df(2L)cl7/+, Df(2L)cl7/bchs17, bchs17/bchs12 or bchs17/+.
The microchaeta loss of Rab11ex1/Rab1193Bi flies is significantly suppressed by Df(2L)cl7/+ or bchs17/+ and is completely suppressed by Df(2L)cl7/bchs17 or bchs17/bchs12. Further, posterior scutellar bristle length of Rab11ex1/Rab1193Bi flies is restored partially by Df(2L)cl7/+ or bchs17/+ and more fully by Df(2L)cl7/bchs17 or bchs17/bchs12.
The microchaeta loss of Rab1193Bi flies is significantly suppressed by bchs58/+ or bchs8K/+ and is completely suppressed by bchs58/bchs58.
The bouton density and branching defects of Rab11ex1/Rab1193Bi larval NMJs at muscle 6/7 are significantly suppressed in bchs17/bchs12; Rab11ex1/Rab1193Bi double mutants.
Rab1193Bi/Rab11ETo11 is rescued by Rab11GFP
Rab1193Bi/Rab11ETo3 or Rab1193Bi/Rab11ETo11 flies carrying Rab11T:Avic\GFP are fully viable and testes from larvae of these genotypes do not exhibit abnormal spermatids.
T. Vincent
Order of alleles (based on transheterozygous sterile phenotype): Rab1193Bi < Rab11j2D1 < Rab11EP3017 = Rab11ETo11 = Rab11ETo3 < Df(3R)e-N19.