A Database of Drosophila Genes & Genomes

FB2013_03, released May 7th, 2013
 

Allele Dmel\chb4

General Information
SymbolDmel\chb4SpeciesD. melanogaster
NameFlyBase IDFBal0104955
Feature typealleleAssociated geneDmel\chb
Also Known Asorbit4
Allele classamorphic allele - genetic evidence
MutagenDelta2-3
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Description
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FB2013_03
FB2013_02
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Allele class
Mutagen
Mutations Mapped to the Genome
Type
Location
Additional Notes
References
Associated Sequence Data
DDBJ /
EMBL /
GenBank
DNA sequence
Protein sequence
Name
 
UniProtKB/Swiss-Prot
UniProtKB/TrEMBL
Progenitor genotype
Nature of the lesion
Statement
Reference
Imprecise excision of the P{lacW} element, resulting in a deletion extending from within the asparagine-synthetase gene to within the chb gene.
Caused by aberration
Cytology
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Statement
Reference
Homozygous and chb2/chb4 embryos show ectopic crossing of the midline by axons in the central nervous system. pCC axons often orient towards the midline in mutant embryos (in contrast to wild type where pCC axons extend slightly away from the midline) and sometimes crosses the midline to meet its contralateral homologue. Mutant embryos occasionally show premature arrest of the ISNb axon, at the muscle 13 cleft.
Mitotic defects are seen in the cells of the larval central nervous system in chb4/chbS068607 flies. Polyploid metaphase figures (15%), diploid metaphase figures with hypercondensed chromosomes (4%) and circular metaphase figures (4%) are seen. The metaphase to anaphase ratio and the mitotic index is increased compared to wild type. Third instar chb4/chb2 larvae lack imaginal discs and have a small central nervous system. More than 80% of total metaphase figures are polyploid, and more than 30% of polyploid figures have greater than an 8N chromosome complement. Circular metaphase figures and anaphase figures cannot be detected.
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Statement
Reference
chb4 has neuroanatomy defective phenotype, enhanceable by Abl2
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Statement
Reference
chb4, robo1 has neuroanatomy defective phenotype, non-enhanceable by robo31
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Statement
Reference
chb4 is an enhancer of neuroanatomy defective phenotype of Abl2
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Reference
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Reference
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Statement
Reference
chb4 has embryonic/larval neuron phenotype, enhanceable by Abl2
chb4 has intersegmental nerve phenotype, enhanceable by Abl2
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Statement
Reference
chb4, robo1 has embryonic/larval neuron phenotype, non-enhanceable by robo31
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Statement
Reference
chb4 is an enhancer of embryonic/larval neuron phenotype of Abl2
chb4 is an enhancer of intersegmental nerve phenotype of Abl2
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Statement
Reference
The frequency of axons ectopically crossing the midline in chb4 Abl2 double homozygous embryos is substantially increased compared to the frequency seen in either single homozygote. chb4 Abl2 double homozygous embryos show an increased frequency of premature arrest of the ISNb axon compared to either single homozygote, with the arrest being seen at both the muscle 6/7 and the muscle 13 choice points. sli2 chb4 double heterozygous embryos have axons ectopically crossing the midline. capt10 chb4 double heterozygous embryos do not show a significant increase in axons ectopically crossing the midline compared to controls. robo1 chb4 double heterozygous embryos have axons ectopically crossing the midline. Heterozygosity for learobo2-8 enhances the frequency of axons ectopically crossing the midline that is seen in robo1 chb4 double heterozygous embryos. Heterozygosity for robo31 does not enhance the frequency of axons ectopically crossing the midline that is seen in robo1 chb4 double heterozygous embryos. The ISNb bypass phenotype caused by expression of AblScer\UAS.cFa under the control of Scer\GAL4elav.PLu is reduced by chb4/chb4.
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Bloomington
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Reported As
Symbol Synonym
chb4
 
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Secondary FlyBase IDs
hide References ( 2 )
Research paper
Lee et al., 2004, Neuron 42(6): 913--926
The microtubule plus end tracking protein Orbit/MAST/CLASP acts downstream of the tyrosine kinase Abl in mediating axon guidance. [FBrf0179303]
Inoue et al., 2000, J. Cell Biol. 149(1): 153--166
Orbit, a novel microtubule-associated protein essential for mitosis in Drosophila melanogaster. [FBrf0127132]