FB2024_03 , released June 25, 2024
Allele: Dmel\Sgt1s2383
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General Information
Symbol
Dmel\Sgt1s2383
Species
D. melanogaster
Name
FlyBase ID
FBal0011152
Feature type
allele
Associated gene
Associated Insertion(s)
Carried in Construct
Key Links
Genomic Maps

Allele class
Nature of the Allele
Allele class
Progenitor genotype
Associated Insertion(s)
Cytology
Description

The lesion in Sgt1s2383 mutants results in a five amino acid deletion in the Chord and Sgt1 (CS) domain that mediates Sgt1-Hsp83 protein interactions.

Allele components
Component
Use(s)
Inserted element
Encoded product / tool
Mutations Mapped to the Genome
Curation Data
Variant Molecular Consequences
Associated Sequence Data
DNA sequence
Protein sequence
 
Expression Data
Reporter Expression
Additional Information
Statement
Reference
 
Marker for
Reflects expression of
Reporter construct used in assay
Human Disease Associations
Disease Ontology (DO) Annotations
Models Based on Experimental Evidence ( 0 )
Disease
Evidence
References
Modifiers Based on Experimental Evidence ( 0 )
Disease
Interaction
References
Comments on Models/Modifiers Based on Experimental Evidence ( 0 )
 
Disease-implicated variant(s)
 
Phenotypic Data
Phenotypic Class
Phenotype Manifest In
Detailed Description
Statement
Reference

Sgt1s2383 mutants exhibit a modest decrease in neuroblast number, and larval/pupal lethality.

Sgt1s2383/Df(3R)Exel6147 mutants exhibit a modest decrease in neuroblast number, and larval/pupal lethality.

Sgt1s2383/Sgt1c01428 mutants exhibit a modest decrease in neuroblast number, and larval/pupal lethality.

Sgt1s2383 mutants exhibit slower cell cycle progression, cytokinesis failure, polyploidy, multiple centrosomes, and malformed mitotic spindles. Sgt1s2383 mutants also exhibit defects in neuroblast cell polarity, with Sgt1 being required for establishing apical cortical polarity during prophase. Sgt1s2383 mutants show a strong loss of cortical scrib localization during metaphase and interphase; they also show a loss of the uniform cortical pool of dlg1 protein at interphase and mitosis, with retention of the pol of dlg1 asymmetrically colocalised with raps at the apical cortex at metaphase.

Sgt1s2383 mutant neuroblasts treated with colcemid lack all detectable apical cortical polarity.

Time-lapse imaging of Sgt1s2383 mutant larval neuroblasts show highly abnormal cortical protrusions, misshapen cells, and failure of cytokinesis.

External Data
Interactions
Show genetic interaction network for Enhancers & Suppressors
Phenotypic Class
Enhanced by
Statement
Reference
NOT suppressed by
Statement
Reference
Enhancer of
Statement
Reference
Phenotype Manifest In
Suppressed by
Statement
Reference

Sgt1s2383 has neuroblast phenotype, suppressible by pinsP62

NOT suppressed by
Statement
Reference

Sgt1s2383 has neuroblast phenotype, non-suppressible by sqhE21.Tag:FLAG

Suppressor of
Statement
Reference

Sgt1s2383 is a suppressor of neuroblast phenotype of pinsP62

Other
Additional Comments
Genetic Interactions
Statement
Reference

Sgt1s2383 rapsP62 double mutant neuroblasts establish little or no apical or basal cortical polarity. The developmental consequences of this loss of polarity are the formation of ectopic neuroblasts throughout the brain. This is in striking contrast to either single mutant, where the brains are smaller with reduced neuroblast numbers.

The presence of sqhE21.T:Zzzz\FLAG fails to suppress the Sgt1s2383 neuroblast cortical polarity phenotype.

The presence of sqhA20.A21.T:Zzzz\FLAG fails to suppress the Sgt1s2383 neuroblast cortical polarity phenotype.

Xenogenetic Interactions
Statement
Reference
Complementation and Rescue Data
Fails to complement
Comments
Images (0)
Mutant
Wild-type
Stocks (1)
Notes on Origin
Discoverer

M. Scott.

The lethality and defects in neuroblast number which are seen in the l(3)s2383 insertion line do not map to the P{lacW}s2383 insertion (which is at 66E), but instead map to a separate lesion (represented by Sgt1s2383) that maps to 84F6-84F13.

Comments
Comments

This allele was listed in the BDGP database as a lethal or sterile line during the period 1994-1999, but was discarded from the gene disruption project prior to the summary publication (FBrf0111489). Reasons for excluding lines from the collection described in FBrf0111489 include presence of more than one P insertion on the mutant chromosome, separation of lethality (or sterility) from the location of the insertion, and loss of lethality (or sterility) from the stock. Further information is available from http://www.fruitfly.org/bfd/ and from Dr. Spradling (spradling@mail1.ciwemb.edu).

Complements: l(3)0162901629. Complements: msn03349. Complements: l(3)0626406264. Complements: dally06464. Complements: mRpL1210534. Complements: mRpL12j4B2.

External Crossreferences and Linkouts ( 0 )
Synonyms and Secondary IDs (3)
Reported As
Symbol Synonym
Sgt1s2383
l(3)s2383s2383
Name Synonyms
Secondary FlyBase IDs
    References (3)