A Database of Drosophila Genes & Genomes

FB2013_03, released May 7th, 2013
 

Allele Dmel\Cdc422

General Information
SymbolDmel\Cdc422SpeciesD. melanogaster
NameFlyBase IDFBal0062065
Feature typealleleAssociated geneDmel\Cdc42
Map ( GBrowse ) GBrowse View Helpdetailed view FBal0062066 FBal0062062 FBal0062061 FBal0062065 FBal0062063 FBal0062064
Allele classhypomorphic allele - genetic evidence
Mutagenethyl methanesulfonate
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Description
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FB2013_03
FB2013_02
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hide Nature of the Allele
Allele class
Mutagen
Mutations Mapped to the Genome
Type
Location
Additional Notes
References
point mutation
evidence=experimental
reported_na_change=T311A
na_change=T19592280A
Associated Sequence Data
DDBJ /
EMBL /
GenBank
DNA sequence
Protein sequence
Name
UniProtKB/Swiss-Prot
UniProtKB/TrEMBL
Progenitor genotype
Nature of the lesion
Statement
Reference
Nucleotide substitution: T311A. Mutation in splice donor consensus site.
Mutation in the splice donor sequence of the small internal intron.
Cytology
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hide Phenotype Manifest In
actin filament & rhabdomere | somatic clone
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Statement
Reference
The hatching rate of eggs derived from homozygous females is reduced compared to wild type, regardless of the zygotic state.
Mutant larvae fail to encapsulate eggs when parasitised by the avirulent L. boulardi wasp strain G486 (no melanisation is seen). Plasmatocytes and lamellocytes fully cover the egg.
Homozygous larvae fail to encapsulate eggs of the avirulent wasp strain L. boulardi G486. Isolated plasmatocytes from homozygous larvae show a reduced ability to phagocytose E. coli and S. aureus in a phagocytosis assay.
Cdc42[2] heterozygous larvae exhibit wild-type neuromuscular junction length and total bouton number, but satellite bouton formation is slightly elevated.
Cdc42[2] third instar larvae exhibit synaptic overgrowth and an increase in bouton number in segment A3, muscle 6/7 compared to controls.
Cdc42[4]/Cdc42[2] flies show normal resistance to infection with P.aeruginosa by septic injury.
Cdc422 mutants exhibit a delay in F-actin enrichment and accumulation in rhabdomeres.
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Linkouts
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hideEnhanced by
Statement
Reference
Cdc422 has neuroanatomy defective phenotype, enhanceable by Cip41/Cip4[+]
Cdc422 has neuroanatomy defective phenotype, enhanceable by Cip41/WASp[+]/WASp1/Cip4[+]
hideSuppressed by
Statement
Reference
hideEnhancer of
Statement
Reference
Cdc42[+], Cip41, Cip4[+], Cdc422 is an enhancer of neuroanatomy defective phenotype of WASp1
Cdc42[+], WASp[+], Cdc422, WASp1 is an enhancer of neuroanatomy defective phenotype of WASp1
Cdc42[+], WASp[+], WASp1, Cdc422 is an enhancer of neuroanatomy defective phenotype of Cip41
Cdc42[+]/Cdc422 is an enhancer of neuroanatomy defective phenotype of Cip41
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Statement
Reference
hide Phenotype Manifest In
hideEnhanced by
Statement
Reference
Cdc422 has neuromuscular junction phenotype, enhanceable by Cip41/Cip4[+]
Cdc422 has neuromuscular junction phenotype, enhanceable by Cip41/WASp[+]/WASp1/Cip4[+]
Cdc422 has NMJ bouton phenotype, enhanceable by Cip41/Cip4[+]
Cdc422 has NMJ bouton phenotype, enhanceable by Cip41/WASp[+]/WASp1/Cip4[+]
hideSuppressed by
Statement
Reference
hideNOT suppressed by
Statement
Reference
Cdc422 has phenotype, non-suppressible by Merhs.PM
hideEnhancer of
Statement
Reference
Cdc42[+], Cip41, Cip4[+], Cdc422 is an enhancer of neuromuscular junction phenotype of WASp1
Cdc42[+], Cip41, Cip4[+], Cdc422 is an enhancer of NMJ bouton phenotype of WASp1
Cdc42[+], WASp[+], WASp1, Cdc422 is an enhancer of neuromuscular junction phenotype of Cip41
Cdc42[+], WASp[+], WASp1, Cdc422 is an enhancer of NMJ bouton phenotype of Cip41
Cdc42[+]/Cdc422 is an enhancer of neuromuscular junction phenotype of Cip41
Cdc42[+]/Cdc422 is an enhancer of NMJ bouton phenotype of Cip41
hideSuppressor of
Statement
Reference
Cdc42[+]/Cdc422 is a suppressor of cycle 14 embryo phenotype of CycB+t10
hideNOT Suppressor of
Statement
Reference
Cdc42[+]/Cdc422 is a non-suppressor of aster | embryonic cycle 5 phenotype of CycB+t10
Cdc42[+]/Cdc422 is a non-suppressor of aster | embryonic cycle 6 phenotype of CycB+t10
Cdc42[+]/Cdc422 is a non-suppressor of aster | embryonic cycle 7 phenotype of CycB+t10
Cdc42[+]/Cdc422 is a non-suppressor of cycle 10 embryo phenotype of CycB+t10
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hide Genetic Interactions
Statement
Reference
Zir[BG00267]/+ ; Cdc42[2]/+ double heterozygous larvae have a reduced rate of encapsulation (37%) of eggs of the avirulent wasp strain L. boulardi G486 compared to the rate seen in either single heterozygote.
Cdc42[2]; Cip4[1] double heterozygotes exhibit an increase in total bouton number, satellite bouton formation and neuromuscular junction length. Cdc42[2]/+; Cip4[1]/+; WASp[1]/+ trans-heterozygous larvae exhibit an increase in total bouton number, neuromuscular junction length and in particular satellite bouton formation.
Cdc42[2] nwk[1] double mutants exhibit more severe synaptic overgrowth and an increased number of boutons and satellite boutons compared to either single mutant. Cdc42[2] nwk[2] double mutants exhibit more severe synaptic overgrowth and an increased number of boutons and satellite boutons compared to either single mutant. Cdc42[2] nwk[2]/nwk[1] double mutants exhibit an increased number of satellite boutons in segment A2-A3, muscle 4 compared to either Cdc42[2] or nwk[2] homozygous single mutants. Expression of Cdc42[Ubi-p63E.T:Hsap\MYC] rescues the synaptic overgrowth and increased bouton and satellite bouton number phenotypes seen in nwk[2] Cdc42[2] double mutant larvae.
The Cdc422 mutation fails to modify the cv-cM62 phenotype in the Malpighian tubules.
A Cdc422/+ background enhances the splitting wing hair phenotype of flies that express trcT453A.Scer\UAS under the control of Scer\GAL4ap-md544.
Not rescued by Merhs.PM.
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Statement
Reference
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Rescued by
Comments
hide Stocks ( 1 )
Bloomington
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Discoverer
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Other Crossreferences
Linkouts
hide Synonyms & Secondary IDs ( 4 )
Reported As
Symbol Synonym
Name Synonym
Secondary FlyBase IDs
hide References ( 13 )
Research paper
Leibfried et al., 2013, Development 140(2): 362--371
A Cdc42-regulated actin cytoskeleton mediates Drosophila oocyte polarization. [FBrf0220348]
Howell et al., 2012, Immunogenetics 64(2): 155--161
A directed miniscreen for genes involved in the Drosophila anti-parasitoid immune response. [FBrf0217123]
Sampson et al., 2012, Dev. Comp. Immunol. 38(1): 160--168
The RhoGEF Zizimin-related acts in the Drosophila cellular immune response via the Rho GTPases Rac2 and Cdc42. [FBrf0219019]
Nahm et al., 2010, J. Neurosci. 30(24): 8138--8150
dCIP4 (Drosophila Cdc42-interacting protein 4) restrains synaptic growth by inhibiting the secretion of the retrograde Glass bottom boat signal. [FBrf0211075]
Frank et al., 2009, Neuron 61(4): 556--569
A presynaptic homeostatic signaling system composed of the Eph receptor, ephexin, Cdc42, and CaV2.1 calcium channels. [FBrf0207531]
Rodal et al., 2008, J. Neurosci. 28(33): 8316--8325
Nervous wreck and Cdc42 cooperate to regulate endocytic actin assembly during synaptic growth. [FBrf0205746]
Avet-Rochex et al., 2007, Genes Cells 12(10): 1193--1204
Rac2 is a major actor of Drosophila resistance to Pseudomonas aeruginosa acting in phagocytic cells. [FBrf0200813]
Denholm et al., 2005, Development 132(10): 2389--2400
crossveinless-c is a RhoGAP required for actin reorganisation during morphogenesis. [FBrf0187455]
He et al., 2005, Mol. Biol. Cell 16(2): 689--700
The tricornered Ser/Thr protein kinase is regulated by phosphorylation and interacts with furry during Drosophila wing hair development. [FBrf0184141]
Zelhof and Hardy, 2004, J. Cell Biol. 164(3): 417--426
WASp is required for the correct temporal morphogenesis of rhabdomere microvilli. [FBrf0167774]
Ji et al., 2002, Genetics 162(3): 1179--1195
A genetic screen for suppressors and enhancers of the Drosophila cdk1-cyclin B identifies maternal factors that regulate microtubule and microfilament stability. [FBrf0155492]
Genova et al., 2000, Dev. Biol. 221(1): 181--194
Functional analysis of cdc42 in actin filament assembly, epithelial morphogenesis, and cell signaling during Drosophila development. [FBrf0127090]
Fehon et al., 1997, Genetics 146(1): 245--252
Isolation of mutations in the Drosophila homologues of the human Neurofibromatosis 2 and yeast CDC42 genes using a simple and efficient reverse-genetic method. [FBrf0093443]