Amino acid replacement: A532D.
C8712009A
A532D | raw-PA; A348D | raw-PB; A532D | raw-PC; A375D | raw-PD; A532D | raw-PE
A532D
Site of nucleotide substitution in mutant inferred by FlyBase curator based on reported amino acid change.
rawdcp-1 in transheterozygosity with Df(2L)BSC204, but not with Df(2L)BSC688, Df(2L)Exel6011, Df(2L)BSC109, Df(2L)BSC354 or Df(2L)ED775, provides protection against (injury-induced) Wallerian degeneration of third instar larval axons.
rawdcp-1 homozygotes show protection against (injury-induced) Wallerian degeneration of third instar larval motor and class IV sensory neurons; axons and synapses remain intact for at least 48h after injury and axonal growth at 20h after injury is similar to uninjured controls; neuromuscular junctions exhibit robust evoked EJPs, spontaneous mEJPs and quantal content at 20h after injury, similar to uninjured controls.
rawdcp-1/raw134.47 and rawdcp-1/raw155.27 transheterozygotes also show protection against (injury-induced) Wallerian degeneration of third instar larval motor neurons.
Unlike controls, rawdcp-1/raw134.47 transheterozygotes expressing rawUASp.RA under the control of Scer\GAL4Toll-6-D42 or Scer\GAL4BG380 sustain some neurotransmission at the third instar larval neuromuscular junction at 20h after injury.
rawdcp-1 has abnormal neuroanatomy | recessive | third instar larval stage | conditional phenotype, suppressible | partially by hiwΔN
rawdcp-1 has abnormal neuroanatomy | recessive | third instar larval stage | conditional phenotype, suppressible | partially by Scer\GAL4tey-5053A/kayFbz.UAS
rawdcp-1 has abnormal neuroanatomy | recessive | third instar larval stage | conditional phenotype, suppressible | partially by Scer\GAL4tey-5053A/JraJbz.UAS
rawdcp-1 has abnormal neuroanatomy | recessive | third instar larval stage | conditional phenotype, non-suppressible by Scer\GAL4tey-5053A/NmnatGD8082
rawdcp-1 has abnormal neuroanatomy | recessive | third instar larval stage | conditional phenotype, non-suppressible by Scer\GAL4tey-5053A/bskK53R.UAS
rawdcp-1/raw134.47 is a non-enhancer of abnormal neuroanatomy | larval stage phenotype of Hsap\SARM1SAM.TIR.UAS.Venus, Scer\GAL4tey-5053A
rawdcp-1/raw134.47 is a non-suppressor of abnormal neuroanatomy | larval stage phenotype of Hsap\SARM1SAM.TIR.UAS.Venus, Scer\GAL4tey-5053A
Scer\GAL4tey-5053A, rawdcp-1, wndGL00282 has abnormal neuroanatomy | third instar larval stage phenotype
Scer\GAL4tey-5053A, kayFbz.UAS, rawdcp-1 has abnormal neuroanatomy | third instar larval stage phenotype
Scer\GAL4tey-5053A, bskK53R.UAS, rawdcp-1 has abnormal neuroanatomy | third instar larval stage phenotype
rawdcp-1 has embryonic/larval motor neuron | third instar larval stage | conditional phenotype, suppressible | partially by hiwΔN
rawdcp-1 has axon | third instar larval stage | conditional phenotype, suppressible | partially by Scer\GAL4tey-5053A/JraJbz.UAS
rawdcp-1 has axon | third instar larval stage | conditional phenotype, suppressible | partially by Scer\GAL4tey-5053A/kayFbz.UAS
rawdcp-1 has embryonic/larval motor neuron | third instar larval stage | conditional phenotype, suppressible | partially by Scer\GAL4tey-5053A/JraJbz.UAS
rawdcp-1 has embryonic/larval motor neuron | third instar larval stage | conditional phenotype, suppressible | partially by Scer\GAL4tey-5053A/kayFbz.UAS
rawdcp-1 has axon | third instar larval stage | conditional phenotype, suppressible | partially by hiwΔN
rawdcp-1 has axon | third instar larval stage | conditional phenotype, non-suppressible by Scer\GAL4tey-5053A/NmnatGD8082
rawdcp-1 has embryonic/larval motor neuron | third instar larval stage | conditional phenotype, non-suppressible by Scer\GAL4tey-5053A/NmnatGD8082
rawdcp-1 has axon | third instar larval stage | conditional phenotype, non-suppressible by Scer\GAL4tey-5053A/bskK53R.UAS
rawdcp-1 has embryonic/larval motor neuron | third instar larval stage | conditional phenotype, non-suppressible by Scer\GAL4tey-5053A/bskK53R.UAS
rawdcp-1/raw134.47 is a non-enhancer of axon | larval stage phenotype of Hsap\SARM1SAM.TIR.UAS.Venus, Scer\GAL4tey-5053A
rawdcp-1/raw134.47 is a non-enhancer of embryonic/larval motor neuron | larval stage phenotype of Hsap\SARM1SAM.TIR.UAS.Venus, Scer\GAL4tey-5053A
rawdcp-1/raw134.47 is a non-suppressor of axon | larval stage phenotype of Hsap\SARM1SAM.TIR.UAS.Venus, Scer\GAL4tey-5053A
rawdcp-1/raw134.47 is a non-suppressor of embryonic/larval motor neuron | larval stage phenotype of Hsap\SARM1SAM.TIR.UAS.Venus, Scer\GAL4tey-5053A
Scer\GAL4tey-5053A, rawdcp-1, wndGL00282 has axon | third instar larval stage phenotype
Scer\GAL4tey-5053A, kayFbz.UAS, rawdcp-1 has axon | third instar larval stage phenotype
Scer\GAL4tey-5053A, bskK53R.UAS, rawdcp-1 has axon | third instar larval stage phenotype
Scer\GAL4tey-5053A, bskK53R.UAS, rawdcp-1 has varicosity | ectopic | third instar larval stage | conditional phenotype
JraJbz.UAS, Scer\GAL4tey-5053A, rawdcp-1 has axon | third instar larval stage phenotype
rawdcp-1 homozygotes show protection against (injury-induced) Wallerian degeneration in third instar larval motor neurons. This phenotype is considerably suppressed by hiwΔN or by the expression of either JraJbz.UAS or kayFbz.UAS under the control of Scer\GAL4tey-5053A; is only very slightly suppressed by the expression of NmnatGD8082 under the control of Scer\GAL4tey-5053A (together with Dicer-2, for efficient RNAI); and is not significantly suppressed by the expression of bskK53R.UAS under the control of Scer\GAL4tey-5053A.
In rawdcp-1 homozygotes that also express either bskK53R.UAS, kayFbz.UAS, JraJbz.UAS or wndGL00282 under the control of Scer\GAL4tey-5053A, injured axons exhibit severely decreased new growth compared to controls. In the bskK53R.UAS setting, injured axons also develop varicosities.
rawdcp-1/raw134.47 is partially rescued by rawUASp.RA/Scer\GAL4Toll-6-D42
rawdcp-1/raw134.47 is partially rescued by rawUASp.RA/Scer\GAL4tey-5053A
rawdcp-1/raw134.47 is partially rescued by Scer\GAL4tey-5053A/rawUASp.RB
rawdcp-1/raw134.47 is not rescued by rawUASp.RB/Scer\GAL4repo
rawdcp-1 has been identified as a second-site mutation on the Dcp-1Prev1 chromosome.