A Database of Drosophila Genes & Genomes

FB2013_03, released May 7th, 2013
 

Allele Dmel\ninaB1

General Information
SymbolDmel\ninaB1SpeciesD. melanogaster
NameFlyBase IDFBal0012988
Feature typealleleAssociated geneDmel\ninaB
Also Known AsninaBP315
Map ( GBrowse ) GBrowse View Helpdetailed view FBal0012990 FBal0012988 FBal0012988 FBal0012988
Allele class
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
na_change=G9527640A
comment=One of 3 amino acid substitutions in this strain
pr_change=E280K|ninaB-PA
reported_na_change=G838A
reported_pr_change=E280K
point mutation
reported_na_change=A1411C
comment=One of 3 amino acid substitutions in this strain
evidence=experimental
na_change=A9528213C
pr_change=M471L|ninaB-PA
reported_pr_change=M471L
point mutation
reported_pr_change=E477A
comment=One of 3 amino acid substitutions in this strain
evidence=experimental
na_change=A9528232C
pr_change=E477A|ninaB-PA
reported_na_change=A1430C
Associated Sequence Data
DDBJ /
EMBL /
GenBank
DNA sequence
Protein sequence
Name
 
UniProtKB/Swiss-Prot
UniProtKB/TrEMBL
Progenitor genotype
Nature of the lesion
Statement
Reference
Amino acid replacement: E280K. Nucleotide substitution: G838A. Amino acid replacement: M471L. Nucleotide substitution: A1411C. Amino acid replacement: E477A. Nucleotide substitution: A1430C.
Cytology
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Statement
Reference
Homozygous flies lack the prolonged depolarising afterpotential (PDA) in the electroretinogram response. In mosaic flies in which the retinal tissue is homozygous for ninaB1 but the rest of the animal is ninaB+, the electroretinogram response is normal (the PDA is restored).
The deep pseudopupil is not visible in homozygous mutant adults, only a weak shadow is detected in the eye. This phenotype can be rescued by supplementing the flies' diet with all-trans retinal.
Superficially like ninaA in aberrant visual physiology, but all eight photoreceptors in each eye facet affected by ninaB; can be restored to wild-type phenotype by dietary supplement of retinal but not by other retinoids.
 
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Statement
Reference
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Statement
Reference
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Rescued by
Not rescued by
Comments
hide Stocks ( 1 )
Bloomington
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Discoverer
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Experiments in recombinant E.coli suggest that it is the G838A substitution that causes the defect.
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hide Synonyms & Secondary IDs ( 2 )
Reported As
Symbol Synonym
ninaB1
 
Name Synonym
Secondary FlyBase IDs
hide References ( 5 )
Research paper
Wang et al., 2007, J. Cell Biol. 177(2): 305--316
Dissection of the pathway required for generation of vitamin A and for Drosophila phototransduction. [FBrf0199300]
Yang and O'Tousa, 2007, Mol. Cell. Neurosci. 35(1): 49--56
Cellular sites of Drosophila NinaB and NinaD activity in vitamin a metabolism. [FBrf0200667]
Meyer et al., 2006, J. Cell Sci. 119(Pt 12): 2592--2603
Subcellular translocation of the eGFP-tagged TRPL channel in Drosophila photoreceptors requires activation of the phototransduction cascade. [FBrf0193744]
Gu et al., 2004, J. Biol. Chem. 279(18): 18608--18613
Drosophila ninaB and ninaD act outside of retina to produce rhodopsin chromophore. [FBrf0174785]
von Lintig et al., 2001, Proc. Natl. Acad. Sci. U.S.A. 98(3): 1130--1135
Analysis of the blind Drosophila mutant ninaB identifies the gene encoding the key enzyme for vitamin A formation in vivo. [FBrf0132439]