A Database of Drosophila Genes & Genomes

FB2013_03, released May 7th, 2013
 

Allele Dmel\GNBP1e03371

General Information
SymbolDmel\GNBP1e03371SpeciesD. melanogaster
NameFlyBase IDFBal0156443
Feature typealleleAssociated geneDmel\GNBP1
Also Known AsGNBP1osi
Map ( GBrowse ) Untitled Document detailed view FBti0041705
Allele classloss of function allele
Mutagen
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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
transposable element insertion site
Associated Sequence Data
DDBJ /
EMBL /
GenBank
DNA sequence
Protein sequence
Name
 
UniProtKB/Swiss-Prot
UniProtKB/TrEMBL
Progenitor genotype
Nature of the lesion
Statement
Reference
Insertion of PBac{RB} into the second exon of GNBP1 at nucleotide 511, corresponding to amino acid 48 of the preprotein or residue 29 of the predicted mature protein.
Caused by insertion
Cytology
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Statement
Reference
Mutant flies are susceptible to S. aureus infection compared to wild-type adults.
Hemolymph clots from GNBP1[e03371] third instar larvae show normal melanization.
Mutant flies show reduced survival compared to wild-type controls after infection with S. aureus.
Survival rates of mutant flies after injection of Enterococcus faecalis and Streptococcus pyogenes are severely compromised and similar to those of Dif mutants.
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Statement
Reference
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Statement
Reference
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Statement
Reference
PGRP-SD[Δ3] GNBP1[e03371] and GNBP1[e03371] PGRP-SA[seml] double mutant flies are extremely susceptible to S. aureus infection compared to wild-type adults.
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Statement
Reference
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Rescued by
Comments
hide Stocks ( 2 )
Bloomington
Harvard
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Discoverer
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Mutants show a significant decrease in the expression of Drs in response to several Gram-positive bacterial strains, but not generally in response to fungi. Dpt expression is normal after a challenge with Gram-negative bacteria. Transfer of hemolymph from wild type to GNBP1e03371 flies restores the inducibility of Drs by Gram-positive challenge. Excision of the PBac{RB} element is accompanied by reversion of the E. faecalis sensitivity mutant phenotype.
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Other Crossreferences
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hide Synonyms & Secondary IDs ( 4 )
Reported As
Symbol Synonym
GNBP1e03371
 
Name Synonym
Secondary FlyBase IDs
hide References ( 8 )
Research paper
El Chamy et al., 2008, Nat. Immunol. 9(10): 1165--1170
Sensing of 'danger signals' and pathogen-associated molecular patterns defines binary signaling pathways 'upstream' of Toll. [FBrf0207060]
Wang et al., 2008, Proc. Natl. Acad. Sci. U.S.A. 105(33): 11881--11886
Peptidoglycan recognition protein-SD provides versatility of receptor formation in Drosophila immunity. [FBrf0205873]
Bidla et al., 2007, J. Cell Sci. 120(7): 1209--1215
Crystal cell rupture after injury in Drosophila requires the JNK pathway, small GTPases and the TNF homolog Eiger. [FBrf0192653]
Gottar et al., 2006, Cell 127(7): 1425--1437
Dual detection of fungal infections in Drosophila via recognition of glucans and sensing of virulence factors. [FBrf0194922]
Wang et al., 2006, EMBO J. 25(20): 5005--5014
Sensing of Gram-positive bacteria in Drosophila: GNBP1 is needed to process and present peptidoglycan to PGRP-SA. [FBrf0194406]
Bischoff et al., 2004, Nat. Immunol. 5(11): 1175--1180
Function of the Drosophila pattern-recognition receptor PGRP-SD in the detection of Gram-positive bacteria. [FBrf0180563]
Gobert et al., 2003, Science 302(5653): 2126--2130
Dual activation of the Drosophila toll pathway by two pattern recognition receptors. [FBrf0168033]
Personal communication to FlyBase
Gene Disruption Project members and Exelixis, 2005, Genomic mapping of Exelixis insertion collection. (Computer file)
Genomic mapping of Exelixis insertion collection. (Computer file) [FBrf0184340]