Single cell MARCM clones of Dscam1unspecified mutant mushroom body alpha/beta neurons do not effectively segregate their sister branches - multiple neurites of the same cellular origin extend into the same mushroom body lobe in 97% of clones.
Scer\GAL4ey-OK107-mediated expression of Dscam1A-17.2-19-23.Scer\UAS.T:Avic\GFP in Dscam1unspecified clones (using the MARCM/GAL80 system) show the multibranch/lobe phenotype in 22% of cases, and a single-branch/neuron phenotype in 13% of cases.
Scer\GAL4ey-OK107-mediated expression of Dscam1A-17.2-19+23.Scer\UAS.T:Avic\GFP in Dscam1unspecified clones (using the MARCM/GAL80 system) show the multibranch/lobe phenotype in 16% of cases, and a single-branch/neuron phenotype in 11% of cases.
Scer\GAL4ey-OK107-mediated expression of Dscam1A-17.2+19-23.Scer\UAS.T:Avic\GFP in Dscam1unspecified clones (using the MARCM/GAL80 system) show the multibranch/lobe phenotype in 25% of cases, and a single-branch/neuron phenotype in 5% of cases.
Scer\GAL4ey-OK107-mediated expression of Dscam1A-17.2+19+23.Scer\UAS.T:Avic\GFP in Dscam1unspecified clones (using the MARCM/GAL80 system) show the multibranch/lobe phenotype in 22% of cases, and a single-branch/neuron phenotype in 5% of cases.
Dscam null mutant homozygotes show loss of glomerular boundaries in the antennal lobe, such that axons of a given olfactory receptor neuron class target more than one glomerulus in each antennal lobe. Discrete glomeruli are still formed, but their stereotyped arrangement within the antennal lobe is highly disrupted.
Sister branches of single Dscamunspecified mushroom body neurons in an otherwise wild-type background show a high frequency of segregation defects, often failing to segregate into the two mushroom body lobes.
Homozygous mutant v'ada neuron clones do not have a significantly different territory size from that of control clones.
Analysis of somatic clones does not reveal obvious mis-targeting errors in Dscamunspecified mutant projection neurons. The dendrites of Dscamunspecified mutant cells innervate the correct DL1 glomerulus. However, compared with controls, Dscamunspecified mutant single cell clones for projection neurons innervating adult antennal lobe DL1 display reduced dendritic elaboration, often only partially innervating the DL1 glomerulus.
In Dscamunspecified mutant vNb clones, the innervation of DA1 and VA1lm is strongly reduced and it is often only partial within the glomeruli.
In Dscamunspecified mutant vNb or single-cell clones, the extent of the dendritic field is substantially reduced: dendrites only innervate the medial part of the antennal lobe. As in uni-glomerular projection neurons, the dendrites are frequently clumped.
All the wild-type single-cell clones analysed elaborate a uniform distribution of dendrites across the entire antennal lobe. By contrast, single Dscamunspecified mutant cells do not evenly innervate all glomeruli. Dendrites in lateral regions are more affected than those in the medial region. Dscamunspecified mutant neuroblast clones containing 5-10 local interneurons also show severe clumping defects of dedritic patterning compared with controls. A massive aggregate of dendrites form as a condensed sphere-like structure within the antennal lobe.
Dscam1unspecified is a non-enhancer of abnormal neuroanatomy | embryonic stage phenotype of mud3
Dscam1unspecified/Dscam1[+] is a suppressor of abnormal touch response phenotype of Fmr1RNAi.UAS.cUa, Scer\GAL4455.2
Dscam1unspecified/Dscam1[+] is a suppressor of abnormal touch perception phenotype of Fmr1RNAi.UAS.cUa, Scer\GAL4455.2
Dscam1unspecified/Dscam1[+] is a suppressor of abnormal neuroanatomy phenotype of Fmr1unspecified
Dscam1unspecified is a non-enhancer of larval ventral nerve cord | embryonic stage phenotype of mud3
Dscam1unspecified is a non-enhancer of larval ventral nerve cord commissure | embryonic stage phenotype of mud3
Dscam1unspecified/Dscam1[+] is a suppressor of mechanosensory neuron phenotype of Fmr1unspecified
Dscam1unspecified/Dscam1[+] is a suppressor of axon | ectopic phenotype of Fmr1unspecified
Dscam1unspecified does not enhance the midline crossing defects of mud3 mutant embryos.
'Dscam[null]'/+ reduces the frequency and type of pSc axonal arbor targeting errors in 'Fmr1[null]' homozygotes.
'Dscam[null]'/+ returns the cleaning response rate of Fmr1dsRNA.Scer\UAS.cUa Scer\GAL4455.2 flies (following stimulation of the posterior scutellar bristles) back to control levels.
Dscam1unspecified is rescued by Dscam1+t73.3
Dscam1unspecified is partially rescued by Dscam1A-17.2-19-23.UAS.GFP/Scer\GAL4ey-OK107
Dscam1unspecified is partially rescued by Scer\GAL4ey-OK107/Dscam1A-17.2-19+23.UAS.GFP
Dscam1unspecified is partially rescued by Scer\GAL4ey-OK107/Dscam1A-17.2+19-23.UAS.GFP
Dscam1unspecified is partially rescued by Scer\GAL4ey-OK107/Dscam1A-17.2+19+23.UAS.GFP
Dscam1unspecified is partially rescued by Scer\GAL4elav-C155/Dscam1UAS.1.30.30.2
Dscam1unspecified is partially rescued by Scer\GAL4elav-C155/Dscam1UAS.11.31.25.2
Dscam1unspecified is not rescued by Scer\GAL4elav-C155/Dscam17.27.25.1.UAS.cZa
Dscam1unspecified is not rescued by Scer\GAL4elav-C155/Dscam1UAS.1.30.30.1
Dscam1unspecified is not rescued by Scer\GAL4elav-C155/Dscam1UAS.11.31.25.1
Dscam1unspecified is not rescued by Scer\GAL4elav-C155/Dscam112.20.19.1.UAS
Scer\GAL4ey-OK107-mediated expression of Dscam1A-17.2-19-23.Scer\UAS.T:Avic\GFP in Dscam1unspecified clones (using the MARCM/GAL80 system) reduces the multibranch/lobe phenotype from 97% to 22% of cases.
Scer\GAL4ey-OK107-mediated expression of Dscam1A-17.2-19+23.Scer\UAS.T:Avic\GFP in Dscam1unspecified clones (using the MARCM/GAL80 system) reduces the multibranch/lobe phenotype from 97% to 16% of cases.
Scer\GAL4ey-OK107-mediated expression of Dscam1A-17.2+19-23.Scer\UAS.T:Avic\GFP in Dscam1unspecified clones (using the MARCM/GAL80 system) reduces the multibranch/lobe phenotype from 97% to 25% of cases.
Scer\GAL4ey-OK107-mediated expression of Dscam1A-17.2+19+23.Scer\UAS.T:Avic\GFP in Dscam1unspecified clones (using the MARCM/GAL80 system) reduces the multibranch/lobe phenotype from 97% to 22% of cases.