FB2024_03 , released June 25, 2024
Aberration: Dmel\Df(3R)ro-XB3
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General Information
Symbol
Df(3R)ro-XB3
Species
D. melanogaster
Name
Deficiency (3R) rough
FlyBase ID
FBab0002886
Feature type
Also Known As
Df(3R)roXB3
Computed Breakpoints include
Sequence coordinates
Member of large scale dataset(s)
Nature of Aberration
Cytological Order
Progenitor
Class of aberration (relative to wild type)
Class of aberration (relative to progenitor)
Breakpoints
Causes alleles
Carries alleles
Transposon Insertions
Formalized genetic data

bk1 << l(3)97Df << l(3)97De << bk2 << Ets97D

Genetic mapping information
Comments
Comments on Cytology

Left limit of break 1 from polytene analysis (FBrf0082809) Right limit of break 1 from inclusion of Tl (FBrf0042050) Limits of break 2 from polytene analysis (FBrf0082809)

Sequence Crossreferences
DNA sequence
Protein sequence
Gene Deletion and Duplication Data
Genes Deleted / Disrupted
Genes NOT Deleted / Disrupted
Genes Duplicated
Complementation Data
Completely duplicated
Partially duplicated
Molecular Data
Completely duplicated
Partially duplicated
Genes NOT Duplicated
Complementation Data
 
Molecular Data
 
Phenotypic Data
In combination with other aberrations

Df(3R)Tl-X/Df(3R)ro-XB3 embryos show altered targeting of the ISNb pathway. The nerve endings at the cleft between muscles 6 and 7 are reduced in size, the nerve terminals synapsed to muscle M12 are greatly reduced and the nerve terminals synapsed to muscle M13 are expanded compared to controls.

Hemocyte density in the hemolymph of Df(3R)Tl-X/Df(3R)ro-XB3 larvae is significantly lower than in the hemolymph of control larvae.

Df(3R)Tl-X/Df(3R)ro-XB3 transheterozygotes are Tl null embryos. RP3 motoneuron axon pathfinding is normal, but the growth cone often misinnervates non-target muscle cells. SNa growth cones develop normally but SNb growth cones lose targeting accuracy. SNb ending at muscle 15/16 cleft appear thicker than normal and innervation at muscle 6/7 cleft is often either missing or reduced in size.

Df(3R)ro-XB3/Df(3R)Tl-X embryos have an altered number of RP neurons. They have ectopically placed motor endings on muscles 6 and 7 and lack normal cleft endings.

NOT in combination with other aberrations

In Df(3R)Tl-X/Df(3R)ro-XB3 embryos, 12.1% of hemisegments lack normal innervation of muscle fibers 7 and 6 (though innervation of muscles 15 and 16 is normal), and 29.4% of hemisegments have ectopic endings on muscle fibers 7 and 6 (compared to 0% for muscles 15 and 16). Aberrant numbers of RP motoneurons were detected in 15.5% of hemisegments per embryo, and the positioning of cells is noticeably more irregular than in wild type. The most common phenotype is a hemisegment missing one RP motoneuron in the position of either RP1 or RP4. 86% of mutant animals examined show this phenotype. Embryos and larvae (both Df(3R)Tl-X/Df(3R)ro-XB3 and deficiency heterozygotes) show an average of 46.1% of hemisegments per larva with one or more errors in the muscle pattern. Errors include duplications, missing fibers and misinserted fibers.

Stocks (0)
Notes on Origin
Discoverer

Peter Lewis.

 
Balancer / Genotype Variants of the Aberration
 
Separable Components
 
Other Comments
 
Synonyms and Secondary IDs (9)
References (36)