FB2024_03 , released June 25, 2024
Allele: Dmel\lncRNA:Hsrω05241
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General Information
Symbol
Dmel\lncRNA:Hsrω05241
Species
D. melanogaster
Name
FlyBase ID
FBal0009533
Feature type
allele
Associated gene
Associated Insertion(s)
Carried in Construct
Also Known As
hsrω05241
Key Links
Genomic Maps

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

This insertion contains a 240bp deletion in the 5' UTR of the CG4408 gene.

P{PZ} insertion at -130bp in the promoter region of Hsrω.

Allele components
Component
Use(s)
Inserted element
Encoded product / tool
Mutations Mapped to the Genome
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 ( 1 )
Comments on Models/Modifiers Based on Experimental Evidence ( 0 )
 
Disease-implicated variant(s)
 
Phenotypic Data
Phenotypic Class
Phenotype Manifest In
Detailed Description
Statement
Reference

Homozygous males do not show any significant clustering of omega speckles in cyst cells of the testes.

FlyBase curator comment: the male sterile and omega speckle phenotypes described in FBrf0199067 as being due to the Hsrω05241 mutation have subsequently been found to be due to a second site mutation on the chromosome (ms(3)2121) and are not due to an effect on Hsrω (see FBrf0205520).

Eyes of Hsrω05241 homozygous flies appear normal externally. However, pseudopupil analysis of adult eyes reveals significant disorganisation of rhabdomeres in the majority of the ommatidial units. The ommatidia and axonal projections in Hsrω05241 homozygous mutants are organised as in wild-type.

FlyBase curator comment: the male sterile phenotype described in FBrf0144961 as being due to the Hsrω05241 mutation has subsequently been found to be due to a second site mutation on the chromosome (ms(3)2121) and is not due to an effect on Hsrω (see FBrf0205520).

No obvious phenotype.

External Data
Interactions
Show genetic interaction network for Enhancers & Suppressors
Phenotypic Class
Phenotype Manifest In
Additional Comments
Genetic Interactions
Statement
Reference

Germline clones homozygous for a 'l(3)05241' chromosome that carries both l(3)0524105241 and lncRNA:Hsrω05241 produce abnormal eggs due to abnormal oogenesis: few eggs are laid, oocytes show vitellogenic phenotype. Lethality of the 'l(3)05241' chromosome carrying both l(3)0524105241 and lncRNA:Hsrω05241 occurs during the L1 and L2 stages.

Xenogenetic Interactions
Statement
Reference

The neurodegeneration phenotype caused by expression of Zzzz\CAG127Q.Scer\UAS.T:Ivir\HA1 under the control of Scer\GAL4GMR.PF is enhanced by Hsrω05241/+.

The severity of the neurodegeneration phenotypes caused by expression of Zzzz\CAG127Q.Scer\UAS.T:Ivir\HA1 under the control of Scer\GAL4GMR.PF are enhanced by Hsrω05241. In the adult eye, in a Hsrω05241/+ background, the eyes are significantly reduced in size and in some cases necrotic lesions are also seen. In the developing eye disc, in a Hsrω05241 homozygous background, a more severe disorganisation of the ommatidial units and their projections is seen; individual ommatidial cellular integrity is lost and axonal connections to the optic stalk appear highly irregular.

The eye degeneration phenotype caused by expression of Hsap\HDQ93.ex1p.Scer\UAS under the control of Scer\GAL4GMR.PF is enhanced by Hsrω05241/Hsrω05241.

Complementation and Rescue Data
Comments
Images (0)
Mutant
Wild-type
Stocks (1)
Notes on Origin
Discoverer

The P{PZ}Hsrω05241 insertion in the promoter of Hsrω is separable from a mutation causing recessive lethality (l(3)0524105241) and also from the ms(3)2121 second site mutation.

In FBrf0144961, it was reported that the P{PZ}Hsrω05241 insertion caused male sterility and an excessive clustering of omega speckles in cyst cells in the testes. However, these phenotypes are in fact caused by the second site ms(3)2121 mutation and are not due to an effect on Hsrω.

Comments
Comments

Complements: mod(mdg4)04143 Complements: mod(mdg4)07038 Complements: E2f07172 Complements: mod(mdg4)L3101 Complements: l(3)neo551

External Crossreferences and Linkouts ( 0 )
Synonyms and Secondary IDs (11)
Reported As
Name Synonyms
Secondary FlyBase IDs
    References (14)