FB2026_01 , released March 12, 2026
FB2026_01 , released March 12, 2026
Allele: Dmel\Lasp1
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General Information
Symbol
Dmel\Lasp1
Species
D. melanogaster
Name
FlyBase ID
FBal0241830
Feature type
allele
Associated gene
Associated Insertion(s)
Carried in Construct
Key Links
Genomic Maps

Mutagen
Nature of the Allele
Caused by aberration
Cytology
Description

Scer\FRT-mediated recombination between the two progenitor insertions has resulted in the deletion of the intervening sequence, which removes the second exon of Lasp and also removes intronic sequences, which include the nested CG9692 transcription unit.

Mutations Mapped to the Genome
Curation Data
Type
Location
Additional Notes
References
Comment:

Deletion created by using piggyBac elements PBac{RB}Laspe00056 and PBac{RB}Laspe03191 for heat shock-mediated FLP/FRT recombination. Location of deletion on reference sequence inferred by FlyBase curator.

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

Indirect flight muscles from Lasp1 and Lasp1/Laspy41 mutants show no gross defects, but sarcomeres as well as thin filaments are 12% shorter than wild type. Myofibrils have an increased diameter, owing to both a 50% increase in the number of filaments and an increase in filament spacing.

The flight ability of 3-5 day old flies is partially impaired and deteriorates in older flies.

In 3-day old Lasp1 flies, I-band appearance in indirect flight muscles appears almost wild type, but in 18-day old flies, the I-band is wider than wild type. 18-day old mutant muscle also displays a thin filament packing/stability defect.

Hub cells fail to localise to the apical tip of the testis in homozygous males. Germ cells are still present in 14 day old mutant males. Cysts coil prematurely and disintegrate into individual sperm at the coiling stage in the mutant males. Filamentous actin is only weakly visible at the assembly stage of actin cones in mutant spermatids. At the migrating stage, filamentous actin is barely visible or not visible at all. The mutant cysts show incomplete and slower spermatid individualisation compared to controls. The individualised spermatids are surrounded by a loose membrane and membrane fragments are found between spermatids.

External Data
Interactions
Show genetic interaction network for Enhancers & Suppressors
Phenotypic Class
Phenotype Manifest In
Enhancer of
Statement
Reference

Lasp[+]/Lasp1 is an enhancer of hub cell phenotype of mys8

Additional Comments
Genetic Interactions
Statement
Reference

mys8 ; Lasp1/+ males show a stronger hub cell mislocalisation phenotype than mys8 males. The double mutant males have wild-type fertility.

Xenogenetic Interactions
Statement
Reference
Complementation and Rescue Data
Comments

Scer\GAL4Mef2.PR-mediated expression of LaspL.Scer\UAS.T:Zzzz\FLAG,T:Zzzz\His6, LaspS.Scer\UAS.T:Zzzz\FLAG,T:Zzzz\His6 or LaspL.Scer\UAS.T:Avic\GFP rescues the sarcomere length and thin filament length phenotypes seen in Lasp1 indirect flight muscles.

Scer\GAL4Mef2.PR-mediated expression of LaspL.Scer\UAS.T:Zzzz\FLAG,T:Zzzz\His6 rescues the reduced flight ability of Lasp1 flies.

Scer\GAL4Mef2.PR-mediated expression of LaspΔLIM.L.Scer\UAS.T:Zzzz\FLAG,T:Zzzz\His6 rescues the sarcomere length, thin filament length, myofibril diameter and flight phenotypes seen in Lasp1 mutants.

Scer\GAL4Mef2.PR-mediated expression of LaspY121S.L.Scer\UAS.T:Zzzz\FLAG,T:Zzzz\His6 cannot rescue the sarcomere length, thin filament length, myofibril diameter or flight phenotypes seen in Lasp1 mutants. EM analyses reveal that filament number, but not filament spacing, is partially rescued.

Scer\GAL4Mef2.PR-mediated expression of LaspΔNEB.L.Scer\UAS.T:Zzzz\FLAG,T:Zzzz\His6 cannot rescue the sarcomere length, thin filament length, myofibril diameter or flight phenotypes seen in Lasp1 mutants.

Scer\GAL4Mef2.PR-mediated expression of LaspΔSH3.L.Scer\UAS.T:Zzzz\FLAG,T:Zzzz\His6 cannot rescue the sarcomere length, thin filament length, myofibril diameter or flight phenotypes seen in Lasp1 mutants.

Scer\GAL4Mef2.PR-mediated expression of LaspY86S.L.Scer\UAS.T:Zzzz\FLAG,T:Zzzz\His6 rescues the sarcomere length, thin filament length and flight phenotypes, but not the myofibril diameter phenotype seen in Lasp1 mutants. EM analyses reveal that filament spacing, but not filament number, is partially rescued.

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Mutant
Wild-type
Stocks (0)
Notes on Origin
Discoverer
External Crossreferences and Linkouts ( 0 )
Synonyms and Secondary IDs (1)
Reported As
Name Synonyms
Secondary FlyBase IDs
    References (2)