FB2024_03 , released June 25, 2024
Allele: Dmel\SuUR+t4.9
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General Information
Symbol
Dmel\SuUR+t4.9
Species
D. melanogaster
Name
FlyBase ID
FBal0135782
Feature type
allele
Associated gene
Associated Insertion(s)
Carried in Construct
Also Known As
X6S1
Key Links
Genomic Maps

Nature of the Allele
Progenitor genotype
Carried in construct
Cytology
Description

4.9kb XbaI-SalI genomic fragment containing SuUR and CG6310 sequences.

Allele components
Component
Use(s)
Regulatory region(s)
Encoded product / tool
Mutations Mapped to the Genome
Curation Data
Type
Location
Additional Notes
References
Linked to:
XbaI-SalI restriction fragment
Comment:

Position of restriction fragment 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

The chromosomal break frequency in the 75C1-2 region is significantly increased in a 2x SuUR+t4.9 background.

Homozygotes show a increased frequency of heterochromatization in the distal parts of the X chromosome of the T(1;2)dorvar7 rearrangement compared to animals which are wild-type for SuUR. Homozygotes show a increased frequency of heterochromatization in the distal parts of the X chromosome of the Dp(1;1)pn2 rearrangement compared to animals which are wild-type for SuUR.

Animals containing four or more doses of SuUR+ (increasing numbers of copies of SuUR+t4.9 in a SuUR+ background) results in a change in the morphology of female salivary gland chromosomes; there are an increased number of ectopic contacts and weak points. Additional copies of SuUR+ increase the frequency of breaks in regions of the polytene chromosomes that already contain weak points in the control strain. In addition, females containing extra copies of SuUR+ have breaks in the polytene chromosomes at numerous new sites where breaks are not seen in the wild type. The total number of weak points increases from 58 in the control strain containing two doses of SuUR+ to 161 in females carrying from four to eight doses of SuUR+. Weak points are absent (with very rare exceptions) in wild-type male X chromosomes, but in males carrying four doses of SuUR+, weak points appear at 17 sites with frequencies between 3% and 50%. The number of sites and frequency of breaks in these males is about half that found in corresponding transgenic females (carrying four doses of SuUR+).

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

2x SuUR+t4.9 does not affect the chromosomal break frequency in the 75C1-2 region of Df(3L)ED225, Df(3L)H99 or the duplicated part of the region present in Dp(3L)NA18. However, 2x SuUR+t4.9 does increase break frequency in Df(3L)ED224 chromosomes from 0% to 5%.

Xenogenetic Interactions
Statement
Reference
Complementation and Rescue Data
Images (0)
Mutant
Wild-type
Stocks (0)
Notes on Origin
Discoverer
External Crossreferences and Linkouts ( 0 )
Synonyms and Secondary IDs (1)
Reported As
Symbol Synonym
SuUR+t4.9
Name Synonyms
Secondary FlyBase IDs
    References (7)