Expression of a coding region made up of amino acids 1-32 of wg (including the signal sequence) fused to AR fused to three Tag:HA tags fused to SLD fused to amino acids 32-536 of unc-5 (extracellular and transmembrane domain) fused to SF fused to amino acids 536-1072 of unc-5 (cytoplasmic domain) is governed by UAS regulatory sequences.
EW neurons misexpressing unc-5Scer\UAS.T:Ivir\HA1,T:SS-wg, under the control of Scer\GAL4eg-Mz360, do not cross the midline but fail to project laterally.
Embryos expressing unc-5Scer\UAS.T:Ivir\HA1,T:SS-wg under the control of Scer\GAL4eve.RN2 do not have guidance defects in the intersegmental nerve.
Expression of unc-5Scer\UAS.T:Ivir\HA1,T:SS-wg under the control of Scer\GAL4repo has no effect on the migration of embryonic peripheral glia. However, ectopic interface glia are frequently seen in the periphery.
Misexpression of unc-5Scer\UAS.T:Ivir\HA1,T:wg, under the control of Scer\GAL4elav.PLu, results in the redirection of the ventral-ISNb branch, which joins the dorsal ISN and projects dorsally. The lateral SNa is not affected.
When unc-5Scer\UAS.T:Ivir\HA1,T:wg is driven by Scer\GAL4ap-md544, ap expressing neurons are driven laterally to exit the ventral nerve cord into the periphery.
When expression is driven by Scer\GAL4elav.PLu commissures are completely lacking from the embryonic CNS, because the commissural axons are prevented from crossing the midline. When expression is driven by Scer\GAL4ap-md544, the axon in which unc-5Scer\UAS.T:Ivir\HA1,T:wg is expressed projects directly away from the midline, as opposed to the wild type situation of it projecting towards the midline.
Df(2R)eve, Scer\GAL4eve.RN2, unc-5UAS.Tag:HA,Tag:SS(wg) has abnormal neuroanatomy phenotype, enhanceable by Fas2UAS.cLa, Scer\GAL4eve.RN2
Nrg180.I.UAS, Scer\GAL4eg-Mz360, unc-5UAS.Tag:HA,Tag:SS(wg) has abnormal neuroanatomy phenotype, enhanceable by beat-IaUAS.cFa, Scer\GAL4eg-Mz360
Scer\GAL4eg-Mz360, unc-5UAS.Tag:HA,Tag:SS(wg) has abnormal neuroanatomy phenotype, enhanceable by Nrg180.I.UAS/beat-IaUAS.cFa, Scer\GAL4eg-Mz360
Nrg180.I.UAS, Scer\GAL4eg-Mz360, beat-IaUAS.cFa, unc-5UAS.Tag:HA,Tag:SS(wg) has abnormal neuroanatomy phenotype, enhanceable by Fas2UAS.cLa, Scer\GAL4eg-Mz360
Scer\GAL4eg-Mz360, unc-5UAS.Tag:HA,Tag:SS(wg) has abnormal neuroanatomy phenotype, enhanceable by Nrg180.I.UAS/beat-IaUAS.cFa/Fas2UAS.cLa, Scer\GAL4eg-Mz360
Scer\GAL4eg-Mz360, unc-5UAS.Tag:HA,Tag:SS(wg) has abnormal neuroanatomy phenotype, enhanceable by eveΔRP2A
Df(2R)eve, Scer\GAL4eve.RN2, unc-5UAS.Tag:HA,Tag:SS(wg) has abnormal neuroanatomy phenotype, enhanceable by beat-IaUAS.cFa, Scer\GAL4eve.RN2
Df(2R)eve, Scer\GAL4eve.RN2, unc-5UAS.Tag:HA,Tag:SS(wg) has abnormal neuroanatomy phenotype, enhanceable by Nrg180.I.UAS, Scer\GAL4eve.RN2
Scer\GAL4elav.PLu, unc-5UAS.Tag:HA,Tag:SS(wg) has abnormal neuroanatomy phenotype, suppressible by NetAunspecified/NetBunspecified
Scer\GAL4ap-md544, unc-5UAS.Tag:HA,Tag:SS(wg) has abnormal neuroanatomy phenotype, suppressible by Df(1)NP5
Scer\GAL4ap-md544, unc-5UAS.Tag:HA,Tag:SS(wg) has abnormal neuroanatomy phenotype, suppressible | partially by fra3/fra4
Scer\GAL4elav.PLu, unc-5UAS.Tag:HA,Tag:SS(wg) has abnormal neuroanatomy phenotype, suppressible by Df(1)NP5
Scer\GAL4elav.PLu, unc-5UAS.Tag:HA,Tag:SS(wg) has abnormal neuroanatomy phenotype, non-suppressible by fra3/fra4
Scer\GAL4elav.PLu, unc-5UAS.Tag:HA,Tag:SS(wg) has abnormal neuroanatomy phenotype, non-suppressible by robo24/robo24
Scer\GAL4ap-md544, unc-5UAS.Tag:HA,Tag:SS(wg) has abnormal neuroanatomy phenotype, non-suppressible by Scer\GAL4ap-md544/fra3/fra4/fraUAS.cKa
Scer\GAL4elav.PLu, unc-5UAS.Tag:HA,Tag:SS(wg) has abnormal neuroanatomy phenotype, non-suppressible by robo11/robo11
Scer\GAL4ap-md544, unc-5UAS.Tag:HA,Tag:SS(wg) has abnormal neuroanatomy phenotype, non-suppressible by robo18/robo11
unc-5UAS.Tag:HA,Tag:SS(wg)/Scer\GAL4eve.RN2 is an enhancer of abnormal neuroanatomy phenotype of eveΔRP2A
unc-5UAS.Tag:HA,Tag:SS(wg), Nrg180.I.UAS, Df(2R)eve, Scer\GAL4eve.RN2 is an enhancer of abnormal neuroanatomy phenotype of Scer\GAL4eve.RN2, beat-IaUAS.cFa
unc-5UAS.Tag:HA,Tag:SS(wg), Fas2UAS.cLa, Df(2R)eve, Scer\GAL4eve.RN2 is an enhancer of abnormal neuroanatomy phenotype of Scer\GAL4eve.RN2, beat-IaUAS.cFa
unc-5UAS.Tag:HA,Tag:SS(wg)/Df(2R)eve, Scer\GAL4eve.RN2 is an enhancer of abnormal neuroanatomy phenotype of Scer\GAL4eve.RN2, beat-IaUAS.cFa
unc-5UAS.Tag:HA,Tag:SS(wg)/Scer\GAL4eve.RN2 is a suppressor | partially of abnormal neuroanatomy | embryonic stage phenotype of grn7L
unc-5UAS.Tag:HA,Tag:SS(wg)/Scer\GAL4eve.RN2 is a suppressor of abnormal neuroanatomy phenotype of eveunspecified
Df(2R)eve, Scer\GAL4eg-Mz360, unc-5UAS.Tag:HA,Tag:SS(wg) has abnormal neuroanatomy phenotype
Nrg180.I.UAS, Scer\GAL4eg-Mz360, unc-5UAS.Tag:HA,Tag:SS(wg) has abnormal neuroanatomy phenotype
Df(2R)eve, Scer\GAL4eve.RN2, unc-5UAS.Tag:HA,Tag:SS(wg) has larval VUM motor neuron phenotype, enhanceable by Fas2UAS.cLa, Scer\GAL4eve.RN2
Nrg180.I.UAS, Scer\GAL4eg-Mz360, unc-5UAS.Tag:HA,Tag:SS(wg) has larval EW neuron phenotype, enhanceable by beat-IaUAS.cFa, Scer\GAL4eg-Mz360
Scer\GAL4eg-Mz360, unc-5UAS.Tag:HA,Tag:SS(wg) has larval EW neuron phenotype, enhanceable by Nrg180.I.UAS/beat-IaUAS.cFa, Scer\GAL4eg-Mz360
Scer\GAL4eg-Mz360, unc-5UAS.Tag:HA,Tag:SS(wg) has larval VUM motor neuron phenotype, enhanceable by eveΔRP2A
Nrg180.I.UAS, Scer\GAL4eg-Mz360, beat-IaUAS.cFa, unc-5UAS.Tag:HA,Tag:SS(wg) has larval EW neuron phenotype, enhanceable by Fas2UAS.cLa, Scer\GAL4eg-Mz360
Scer\GAL4eg-Mz360, unc-5UAS.Tag:HA,Tag:SS(wg) has larval EW neuron phenotype, enhanceable by Nrg180.I.UAS/beat-IaUAS.cFa/Fas2UAS.cLa, Scer\GAL4eg-Mz360
Df(2R)eve, Scer\GAL4eve.RN2, unc-5UAS.Tag:HA,Tag:SS(wg) has larval VUM motor neuron phenotype, enhanceable by beat-IaUAS.cFa, Scer\GAL4eve.RN2
Df(2R)eve, Scer\GAL4eve.RN2, unc-5UAS.Tag:HA,Tag:SS(wg) has larval VUM motor neuron phenotype, enhanceable by Nrg180.I.UAS, Scer\GAL4eve.RN2
Scer\GAL4elav.PLu, unc-5UAS.Tag:HA,Tag:SS(wg) has larval intersegmental nerve phenotype, suppressible by NetAunspecified/NetBunspecified
Scer\GAL4elav.PLu, unc-5UAS.Tag:HA,Tag:SS(wg) has larval anterior commissure phenotype, suppressible by Df(1)NP5
Scer\GAL4elav.PLu, unc-5UAS.Tag:HA,Tag:SS(wg) has larval posterior commissure phenotype, suppressible by Df(1)NP5
Scer\GAL4ap-md544, unc-5UAS.Tag:HA,Tag:SS(wg) has larval ventral nerve cord phenotype, suppressible by Df(1)NP5
Scer\GAL4ap-md544, unc-5UAS.Tag:HA,Tag:SS(wg) has larval ventral nerve cord phenotype, suppressible | partially by fra3/fra4
Scer\GAL4ap-md544, unc-5UAS.Tag:HA,Tag:SS(wg) has larval ventral nerve cord phenotype, non-suppressible by fra3/fra4/fraUAS.cKa
Scer\GAL4ap-md544, unc-5UAS.Tag:HA,Tag:SS(wg) has larval ventral nerve cord phenotype, non-suppressible by robo18/robo11
Scer\GAL4elav.PLu, unc-5UAS.Tag:HA,Tag:SS(wg) has larval anterior commissure phenotype, non-suppressible by fra3/fra4
Scer\GAL4elav.PLu, unc-5UAS.Tag:HA,Tag:SS(wg) has larval anterior commissure phenotype, non-suppressible by robo24/robo24
Scer\GAL4elav.PLu, unc-5UAS.Tag:HA,Tag:SS(wg) has larval anterior commissure phenotype, non-suppressible by robo11/robo11
Scer\GAL4elav.PLu, unc-5UAS.Tag:HA,Tag:SS(wg) has larval posterior commissure phenotype, non-suppressible by fra3/fra4
Scer\GAL4elav.PLu, unc-5UAS.Tag:HA,Tag:SS(wg) has larval posterior commissure phenotype, non-suppressible by robo24/robo24
Scer\GAL4elav.PLu, unc-5UAS.Tag:HA,Tag:SS(wg) has larval posterior commissure phenotype, non-suppressible by robo11/robo11
unc-5UAS.Tag:HA,Tag:SS(wg)/Scer\GAL4eve.RN2 is an enhancer of larval VUM motor neuron phenotype of eveΔRP2A
unc-5UAS.Tag:HA,Tag:SS(wg), Nrg180.I.UAS, Df(2R)eve, Scer\GAL4eve.RN2 is an enhancer of larval VUM motor neuron phenotype of Scer\GAL4eve.RN2, beat-IaUAS.cFa
unc-5UAS.Tag:HA,Tag:SS(wg), Fas2UAS.cLa, Df(2R)eve, Scer\GAL4eve.RN2 is an enhancer of larval VUM motor neuron phenotype of Scer\GAL4eve.RN2, beat-IaUAS.cFa
unc-5UAS.Tag:HA,Tag:SS(wg)/Df(2R)eve, Scer\GAL4eve.RN2 is an enhancer of larval VUM motor neuron phenotype of Scer\GAL4eve.RN2, beat-IaUAS.cFa
unc-5UAS.Tag:HA,Tag:SS(wg)/Scer\GAL4eve.RN2 is a suppressor | partially of larval intersegmental nerve phenotype of grn7L
unc-5UAS.Tag:HA,Tag:SS(wg)/Scer\GAL4eve.RN2 is a suppressor of larval intersegmental nerve phenotype of eveunspecified
Nrg180.I.UAS, Scer\GAL4eg-Mz360, unc-5UAS.Tag:HA,Tag:SS(wg) has larval EW neuron phenotype
Df(2R)eve, Scer\GAL4eg-Mz360, unc-5UAS.Tag:HA,Tag:SS(wg) has larval RP2 motor neuron phenotype
Df(2R)eve, Scer\GAL4eg-Mz360, unc-5UAS.Tag:HA,Tag:SS(wg) has larval DA1 motor neuron phenotype
Scer\GAL4elav.PLu, sli2, unc-5UAS.Tag:HA,Tag:SS(wg) has larval anterior commissure phenotype
Expression of unc-5Scer\UAS.T:Ivir\HA1,T:SS-wg in a Df(2R)eve mutant background, under the control of Scer\GAL4eve.RN2 leads to both aCC and RP2 motor neurons displaying an almost exclusively single exit from the CNS.
Expression of unc-5Scer\UAS.T:Ivir\HA1,T:SS-wg in an eveΔRP2A mutant background results in 11% of hemisegments exhibiting dual motoneuron exit. These mutants exhibit an increase in dorsal projections in 67% of hemisegments.
Co-expression of beat-IaScer\UAS.cFa and unc-5Scer\UAS.T:Ivir\HA1,T:SS-wg in a Df(2R)eve mutant background, under the control of Scer\GAL4eve.RN2 leads to a more robust CNS exit for motor neurons, with many hemisegments displaying exit of both motor neurons. There are two types of exit: unfasciculated, both axons from the same hemisegment chose a different nerve root, or fasciculated, where axons join and exit through the intersegmental nerve root.
Co-expression of unc-5Scer\UAS.T:Ivir\HA1,T:SS-wg and Nrg180.I.Scer\UAS in a Df(2R)eve mutant background, under the control of Scer\GAL4eve.RN2 leads to a more robust CNS exit for motor neurons, with many hemisegments displaying exit of both motor neurons. There are two types of exit: unfasciculated, both axons from the same hemisegment chose a different nerve root, or fasciculated, where axons join and exit through the intersegmental nerve root.
Co-expression of unc-5Scer\UAS.T:Ivir\HA1,T:SS-wg and Fas2Scer\UAS.cLa in a Df(2R)eve mutant background, under the control of Scer\GAL4eve.RN2 leads to a more robust CNS exit for motor neurons, with many hemisegments displaying exit of both motor neurons. There are two types of exit: unfasciculated, both axons from the same hemisegment chose a different nerve root, or fasciculated, where axons join and exit through the intersegmental nerve root.
Co-expression of unc-5Scer\UAS.T:Ivir\HA1,T:SS-wg, beat-IaScer\UAS.cFa and Nrg180.I.Scer\UAS in a Df(2R)eve mutant background, under the control of Scer\GAL4eve.RN2 leads to a more robust CNS exit for motor neurons, with many hemisegments displaying exit of both motor neurons. The number of hemisegments with one neuronal exit is reduced, compared to controls and single and double mutants.
Co-expression of unc-5Scer\UAS.T:Ivir\HA1,T:SS-wg, beat-IaScer\UAS.cFa and Fas2Scer\UAS.cLa in a Df(2R)eve mutant background, under the control of Scer\GAL4eve.RN2 leads to a more robust CNS exit for motor neurons, with many hemisegments displaying exit of both motor neurons. The number of hemisegments with one neuronal exit is reduced, compared to controls and single and double mutants.
Combinatorial misexpression of unc-5Scer\UAS.T:Ivir\HA1,T:SS-wg with Nrg180.I.Scer\UAS under the control of Scer\GAL4eg-Mz360, results in lateral exit of 8% of EW axons.
Triple misexpression of unc-5Scer\UAS.T:Ivir\HA1,T:SS-wg, beat-IaScer\UAS.cFa, and Nrg180.I.Scer\UAS in EW neurons, under the control of Scer\GAL4eg-Mz360, leads to lateral redirection of axons in 20% of hemisegments.
Quadrupal misexpression of unc-5Scer\UAS.T:Ivir\HA1,T:SS-wg, beat-IaScer\UAS.cFa, Nrg180.I.Scer\UAS and Fas2Scer\UAS.cLa in EW neurons, under the control of Scer\GAL4eg-Mz360, leads to lateral redirection of axons in 33% of hemisegments.
The defects in intersegmental nerve innervation of muscles 1/9 are partially rescued by expression of unc-5Scer\UAS.T:Ivir\HA1,T:SS-wg under the control of Scer\GAL4eve.RN2.
The ventral-ISNb branch projection phenotype is suppressed when unc-5Scer\UAS.T:Ivir\HA1,T:wg is expressed, under the control of Scer\GAL4elav.PLu, in a NetA, NetB double mutant background.
unc-5UAS.Tag:HA,Tag:SS(wg)/Scer\GAL4cas-3921 partially rescues unc-58
unc-5UAS.Tag:HA,Tag:SS(wg)/Scer\GAL4repo partially rescues unc-58
unc-5UAS.Tag:HA,Tag:SS(wg)/Scer\GAL4elav.PLu partially rescues unc-58/unc-52
The expression of unc-5Scer\UAS.T:Ivir\HA1,T:SS-wg under the control of Scer\GAL4Mef2.247 rescues the unc-58 homozygous embryonic heart cardioblast defects (i.e. migration velocity and in filopodial and lamellopodial extensions and activities) and embryonic heart lumen formation defects.
Expression of unc-5Scer\UAS.T:Ivir\HA1,T:SS-wg under the control of Scer\GAL4cas-3921 in unc-58 embryos rescues the normal number of six embryonic peripheral glia distal to the SNc in 49% of hemisegments (compared to only 6% of hemisegments in unc-58 embryos) and five ePG are found distal to the SNc in 39% of hemisegments (compared to only 24% of hemisegments in unc-58 embryos).
Expression of unc-5Scer\UAS.T:Ivir\HA1,T:SS-wg under the control of Scer\GAL4repo in unc-58 embryos rescues the normal number of six embryonic peripheral glia distal to the SNc in 49% of hemisegments (compared to only 6% of hemisegments in unc-58 embryos) and five ePG are found distal to the SNc in 33% of hemisegments (compared to only 24% of hemisegments in unc-58 embryos).
Expression of unc-5Scer\UAS.T:Ivir\HA1,T:wg, under the control of Scer\GAL4elav.PLu, partially rescues the ISN and SNa defects of unc-52/unc-58 mutants.
Four out of four inserts tested gave completely penetrant phenotype with single copy of construct.