A Database of Drosophila Genes & Genomes

FB2013_03, released May 7th, 2013
 

Allele Dmel\inaDP215

General Information
SymbolDmel\inaDP215SpeciesD. melanogaster
NameFlyBase IDFBal0005607
Feature typealleleAssociated geneDmel\inaD
Map ( GBrowse ) GBrowse View Helpdetailed view FBal0062793 FBal0005607 FBal0005607 FBal0062794
Allele class
Mutagenethyl methanesulfonate
hide Recent Updates
Description
What does this section display?
This section contains items that were added to this record for each release. It currently only tracks new links between this FlyBase report and other FlyBase data classes (e.g. genes, references, stocks) or controlled vocabulary terms (e.g. GO, anatomy terms).
What does this section not display?
This section does not currently display links that were removed or gene model changes.
Update Feed
Click the icon below to subscribe to this FlyBase record and receive updates automatically through your feed reader.
FB2013_03
FB2013_02
All updates Click here to see a list of all updates to this record from FB2010_08 and on.
hide Nature of the Allele
Allele class
Mutagen
Mutations Mapped to the Genome
Type
Location
Additional Notes
References
point mutation
pr_change=M442K|inaD-PA
reported_pr_change=M442K
comment=Site of nucleotide substitution in mutant inferred by FlyBase based on reported amino acid change.
evidence=experimental
na_change=T18744172A
point mutation
na_change=T18744172A
reported_na_change=T?A
pr_change=M442K | inaD-PA; M454K | inaD-PB
reported_pr_change=M442K
Associated Sequence Data
DDBJ /
EMBL /
GenBank
DNA sequence
Protein sequence
Name
 
UniProtKB/Swiss-Prot
UniProtKB/TrEMBL
Progenitor genotype
Nature of the lesion
Statement
Reference
Missense mutation in the third PDZ domain.
Cytology
hide Phenotypic Data
hide Phenotypic Class
hide Phenotype Manifest In
hide Detailed Description
Statement
Reference
In inaD1 mutants, individual photoreceptors form the correct number of synapses per presynaptic terminal independently of cartridge composition.
In red-eyed inaD[P215] homozygous flies flies dark-adapted for 2 minutes, the electro-retinogram (ERG) response to 2 second bright white-light stimulation displays the initial fast depolarization and maintenance during stimulation seen in wild-type. However, the recovery of polarisation following the end of stimulation is slower than in wild-type. This phenotype is not seen when low light levels are used.
Mutants have defects in the on/off transients of the electroretinogram. Histamine-activated conductance in mutant laminar L1/L2 neurons appears indistinguishable from wild type.
ERG responses are more wild type in peak amplitude, amount of decay during illumination, refractory period and response latency than those of trp2.
The electroretinograms of young inaD1 flies are abnormal; they show a delay in termination of the photoresponse. Exposure to a shorter light stimulus in these flies results in a less severe termination defect.
inaC2 inaD1 double mutants show abnormal ERGs (electroretinograms) with response inactivation; they show a marked reduction in response to a second pulse of light.
Light-dependent retinal degeneration.
norpAC1094S.hs inaD1 double mutants display a profound loss of the visual response.
inaD1 mutants have an electroretinogram (ERG) phenotype that approaches that of trp mutants. Flies show slow deactivation kinetics in response to a flash of light. The mean latency times between stimulus and quantum-bump generation are significantly greater than in wild-type flies, although quantum bumps from inaD1 flies show normal termination kinetics.
Double mutants of inaD1 with trp2 show the same ERG phenotype as trp2 alone.
Patch clamp recordings of homo- and heterozygotes show a slow deactivation of the light-induced current, this defective deactivation is dependent of calcium influx. Photoreceptors show increased sensitivity to dim light. Two copies of P{hsp70-InsD} can completely rescue the wild type physiology of inaD1 heterozygotes, two copies cannot rescue homozygotes.
Semi-dominant mutant of visual physiology, such that the phenotype (re PDA) of heterozygote similar to that produced by other ina homozygotes; inaD homozygotes exhibit ERG response that decays to baseline during bright light stimulus, and off transient is absent.
 
hide External Data
Linkouts
hide Interactions
hide Phenotypic Class
hideOther
Statement
Reference
hide Phenotype Manifest In
hideNOT Suppressor of
Statement
Reference
inaDP215 is a non-suppressor of rhabdomere phenotype of rdgA1
hideOther
Statement
Reference
hide Additional Comments
hide Genetic Interactions
Statement
Reference
Rhabdomeres of trpl302,inaD1 double mutants are intact in 1 day old flies. ERG light responses of trpl302,inaD1 and trpl302,trp2 are small and transient, but the response amplitude of trpl302,inaD1 is significantly smaller than that of trpl302,trp2. Similarly, refractory period and response latency defects are more severe for trpl302,inaD1 than for trpl302,trp2.
hide Xenogenetic Interactions
Statement
Reference
hide Complementation & Rescue Data
Comments
hide Stocks ( 1 )
Bloomington
hide Notes on Origin
Discoverer
hide External Crossreferences & Linkouts
Other Crossreferences
Linkouts
hide Synonyms & Secondary IDs ( 6 )
Reported As
Symbol Synonym
Name Synonym
Secondary FlyBase IDs
hide References ( 22 )
Generate a list of
List References by type
hide Recent research papers (0)
All research papers listed in FlyBase were published before 2011
hide Recent reviews (0)
All reviews listed in FlyBase were published before 2011