FB2024_04 , released June 25, 2024
Aberration: Dmel\Df(3R)E(spl)-rv27
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General Information
Symbol
Df(3R)E(spl)-rv27
Species
D. melanogaster
Name
FlyBase ID
FBab0010447
Feature type
Also Known As
Df(3R)E(spl)RA7.1, E(spl)RA7.1, Df(3R)E(spl)R-A7.1, E(spl)R-A7.1
Computed Breakpoints include
Sequence coordinates
Member of large scale dataset(s)
Nature of Aberration
Cytological Order
Class of aberration (relative to wild type)
Class of aberration (relative to progenitor)
Breakpoints
Causes alleles
Carries alleles
Transposon Insertions
Formalized genetic data

bk1 << m1 << gro << bk2

Genetic mapping information
Comments

34-kb deletion; -15 to +19 kb

Comments on Cytology

Cytologically invisible deletion. Cytologically normal (Knust et al., Dev Biol 122:262--273 ).

Right limit of break 1 from inclusion of HLHm3 (FBrf0065591) Left limit of break 2 from inclusion of E(spl) (FBrf0056226)

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
 
Affected Genes Inferred by Location
    Phenotypic Data
    In combination with other aberrations
    NOT in combination with other aberrations

    Df(3R)E(spl)-rv27 homozygotes and in combination with gro+t10.4 are lethal. Df(3R)E(spl)-rv27 gro+t10.4 clones display an increased microchaete density, occasionally two instead of the single macrochaete can be seen. Homozygous clones fail to differentiate bristles and form scars on the cuticle, sometimes associated with a few mutant epidermal hairs.

    Clones extending to the wing margin in the posteior or anterior portion of the wing cause loss of margin tissue. Clones in the anterior compartment are accompanied by overgrowth and pattern duplication phenotypes.

    In a gro+t9.2 background, Df(3R)E(spl)-rv27/+ has no effect on the bristle loss phenotype of H20/HE31 while Df(3R)E(spl)-rv27/Df(3R)E(spl)-r72.1 suppresses the bristle loss phenotype.

    In clones in the wing, the phenotype depends on where the clone lies. In the anterior compartment all clones abutting the wing margin cause local overgrowth and pattern duplications. Those abutting the wing margin and restricted to dorsal or ventral surfaces cause overgrowth of both dorsal and ventral cells. Clones at the wing margin cause loss of sensory organs and mild scalloping of the margin.

    Hyperplasia of replicating sensory precursors: due to an increased number of ectodermal cells being recruited as sensory precursor cells.

    Homozygotes exhibit a neurogenic phenotype: the entire neuroectoderm and the epidermal connections between the head and trunk are neuralised leaving only a small shield of dorsal epidermis. Transgenes encoding mutant versions of E(spl) and E(spl)m5-HLH reduce the severity of the neurogenic phenotype.

    Increase in SMCs per cluster in embryos lacking the maternal product.

    Lethal in combination with E(spl)1. Homozygotes have extreme neural hyperplasia and suppress the Nspl-1 phenotype.

    Embryonic lethal and lethal in combination with E(spl)1. Homozygotes have extreme CNS and PNS hyperplasia due to low levels of E(spl)+ gene activity and suppress the Nspl-1 phenotype.

    Stocks (0)
    Notes on Origin
    Discoverer

    Knust and Ziemer.

     
    Balancer / Genotype Variants of the Aberration
     
    Separable Components
     
    Other Comments
     
    Synonyms and Secondary IDs (11)
    Reported As
    Name Synonyms
    Secondary FlyBase IDs
      References (19)