FB2024_03 , released June 25, 2024
Allele: Dmel\scb2
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General Information
Symbol
Dmel\scb2
Species
D. melanogaster
Name
FlyBase ID
FBal0015261
Feature type
allele
Associated gene
Associated Insertion(s)
Carried in Construct
Key Links
Allele class
Nature of the Allele
Allele class
Progenitor genotype
Cytology
Description
Mutations Mapped to the Genome
Curation Data
Type
Location
Additional Notes
References
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

Adult-generated scb2 homozygous mutant intestinal stem cell clones have reduced maintenance 7 days and 14 days after clone induction compared to control clones; remaining clones contain fewer cells by day 14; enteroendocrine cell/enterocyte ratio is unaffected and intestinal stem cells show no obvious signs of apoptosis.

Mutant embryos show a reduced level of phagocytosis of apoptotic cells compared to controls.

The cardioblasts of the heart region of the dorsal vessel in homozygous stage embryos show a less regular alignment of their nuclei along the midline in mutant embryos compared to wild type. No lumen develops between contralaterally apposed cardioblasts in the heart region of mutant embryos, in contrast to wild type. The leading edge membrane of migrating mutant cardioblasts shows less vigorous activity than that of wild-type cardioblasts.

Mutant embryos have no severe defects in salivary gland shape or positioning.

Germ-line clones exhibit a U shaped embryonic phenotype at low penetrance (about 4.5%) suggesting germ band retraction defects. scb5J38/scb2 embryos also exhibit a U shaped embryonic phenotype at low penetrance (about 4%). scb2/Df(2R)Jp1 show the same phenotype at 11% penetrance.

The germ band twists laterally, rather than extending dorsally as in wild type. Proper orientation of the germ band in recovered by the completion of germ-band extension. Embryos exhibit mislocalisation of the pericardial cells and there are fewer of these cells than in wild type. Embryos exhibit significant gaps in the dorsal trunk of the trachea. Embryos frequently display one salivary gland misshapen and smaller than the other, the gland may also be shifted closer to the midline.

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

scb2/scb[+] is an enhancer of visible | dominant phenotype of sogEP7

scb2/scb[+] is an enhancer of visible | dominant phenotype of sogEP11

Suppressor of
Statement
Reference
NOT Suppressor of
Statement
Reference

scb2 is a non-suppressor of lethal | pupal stage phenotype of Cskj1D8/CskS030003

Other
Phenotype Manifest In
Enhanced by
Statement
Reference

scb2 has embryo | germline clone phenotype, enhanceable by wb4Y18

Enhancer of
Statement
Reference

scb2/scb[+] is an enhancer of wing vein phenotype of sogEP7

scb2/scb[+] is an enhancer of wing vein phenotype of sogEP11

scb2 is an enhancer of embryo | germline clone phenotype of wb4Y18

Suppressor of
Statement
Reference

scb2 is a suppressor of eye disc & S phase phenotype of CycEJP

scb2/scb[+] is a suppressor of eye phenotype of CycEJP

Other
Additional Comments
Genetic Interactions
Statement
Reference

mys1/+ ; scb2/+ and vkgp1003-83/scb2 double heterozygous embryos show defects in continuity and alignment of the cardioblasts at the dorsal midline.

LanA9-32/+ ; scb2/+ and wbSF11/scb2 double heterozygous embryos show defects in alignment of the cardioblasts at the dorsal midline.

Significant overgrowth of the neuromuscular junction (NMJ) (increased bouton number per muscle area and increased NMJ length per muscle area) is seen in scb2/+ FakN30/FakKG00304 third instar larvae.

Suppresses the S phase defects seen in the CycEJP eye disc.

Salivary glands in mewM6 scb2 mutant embryos are indistinguishable from those in mewM6 embryos.

Heterozygosity for scb2 does not result in lethality in Abl1/+ embryos derived from homozygous Abl1 female germline clones.

ifB4 scb2 double mutant embryos show no difference in midgut development compared to ifB4 single mutant embryos. mewM6 scb2 double mutant embryos show a strong defect in the migration of the endodermal midgut cells, with a delay in migration of approximately 2 hours (similar to that observed in embryos lacking both maternal and zygotic mys function).

Xenogenetic Interactions
Statement
Reference
Complementation and Rescue Data
Partially rescued by
Comments

Expression of scbScer\UAS.cVa under the control of Scer\GAL4Mef2.PR partially restores lumen formation between cardioblasts in the heart region of scb2/scb2 embryos.

Images (0)
Mutant
Wild-type
Stocks (3)
Notes on Origin
Discoverer
External Crossreferences and Linkouts ( 0 )
Synonyms and Secondary IDs (3)
References (22)