FB2026_01 , released March 12, 2026
FB2026_01 , released March 12, 2026
Allele: Dmel\phylUAS.cPa
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General Information
Symbol
Dmel\phylUAS.cPa
Species
D. melanogaster
Name
Saccharomyces cerevisiae UAS construct a of Pi
FlyBase ID
FBal0126345
Feature type
allele
Associated gene
Associated Insertion(s)
Carried in Construct
Also Known As
UAS-phyl
Key Links
Transgenic product class
Nature of the Allele
Transgenic product class
Progenitor genotype
Carried in construct
Cytology
Description

UAS regulatory sequences drive expression of phyl.

Allele components
Component
Use(s)
Encoded product / tool
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

mesothoracic tergum & microchaeta | ectopic, with Scer\GAL4Eq

wing vein L3 & chaeta | ectopic, with Scer\GAL4dpp.blk1

Detailed Description
Statement
Reference

Adulthood-only expression of phylScer\UAS.cPa under the control of Scer\GAL4esg-NP5130 (using Gal80[ts] for the temporal control of expression) leads to a severe increase in the number of enteroendocrine cells and to a small but significant increase in the intestinal stem cell and enteroblast population in the adult midgut, as compared to controls; after 2 weeks, this expression leads to the development of multilayered tumors of enteroendocrine cell-like cells. Adulthood-only expression under the control of Scer\GAL4Dl-05151-G or Scer\GAL4Su(H).GBE (also using Gal80[ts]) also leads to a severe or small increase, respectively, in the number of enteroendocrine cells in the adult midgut and in the number of mitotic cells, as compared to controls; phylScer\UAS.cPa, Scer\GAL4Su(H).GBE cells are significantly more numerous and lack enteroendocrine-fate markers, as compared to Scer\GAL4Su(H).GBE-only controls.

Clonal expression of phylScer\UAS.cPa under the control of Scer\GAL4Act.PU in the adult midgut leads to the clones exhibiting severe increases in the proportion of enteroendocrine cells and intestinal stem cells, as well as mitotic cells, as compared to control clones and neighboring control tissue.

Overexpression of phylScer\UAS.cPa by Scer\GAL4Eq1 induces ectopic external sensory organs on the notum, in particular, in the midline region.

Expression of phylScer\UAS.cPa under the control of Scer\GAL4dpp.blk1 has no effect on the morphology of the L3 vein.

Expression of phylScer\UAS.cPa under the control of both Scer\GAL4twi.PB and Scer\GAL4Mef2.PR results in alterations in muscle identities in embryos. Muscles DT1 and LT4 consistently have altered morphology and muscle LL1 is occasionally affected. Muscle DT1 fails to attach normally, resulting in a "ball of muscle" phenotype. LT4 fails to grow dorsally, resulting in a smaller muscle than normal.

Expression of phylScer\UAS.cPa under the control of Scer\GAL4Eq1 results in ectopic bristles on the notum; there is a 30-70% increase in the number of notal microchaetae, with a highest density in the midline region. Expression of phylScer\UAS.cPa under the control of Scer\GAL4dpp.blk1 results in ectopic bristles on the scutellum and third wing vein. Supernumerary sensory neurons are produced in the embryo when phylScer\UAS.cPa is expressed under the control of Scer\GAL4sca-537.4. This increase in the number of neurons is due to transformation of outer support cells. Expression of phylScer\UAS.cPa under the control of Scer\GAL4sca-109-68 results in microchaetae in which the outer hair and socket structures are missing and have been transformed into neurons and sheath cells.

External Data
Interactions
Show genetic interaction network for Enhancers & Suppressors
Phenotypic Class
Phenotype Manifest In
Enhanced by
Statement
Reference
NOT Enhanced by
Suppressed by
Statement
Reference

Scer\GAL4Eq, phylUAS.cPa has mesothoracic tergum & microchaeta | ectopic phenotype, suppressible by ttkp69.UAS/Scer\GAL4Eq

Enhancer of
Suppressor of
NOT Suppressor of
Other
Additional Comments
Genetic Interactions
Statement
Reference

The increased numbers of adult midgut enteroendocrine cells, intestinal stem cells and enteroblasts resulting from the adulthood-only expression of phylScer\UAS.cPa under the control of Scer\GAL4esg-NP5130 (using Gal80[ts] for the temporal control of expression) is suppressed by the co-expression of sinaKK107603. The increased number of enteroendocrine cells is also suppressed by the co-expression of ttkScer\UAS.T:Zzzz\FLAG.

The increased number of enteroendocrine cells in adult midgut clones expressing phylScer\UAS.cPa under the control of Scer\GAL4Act.PU is suppressed by Df(1)sc-B57 homozygosity; these rescued clones are composed of small progenitor cells.

The co-expression of phylScer\UAS.cPa partially suppresses the small size and cell number of adult midgut clones expressing scScer\UAS.cPa under the control of Scer\GAL4Act.PU.

The presence of chnEPC05-441 enhances the phylScer\UAS.cPa (under the control of Scer\GAL4Eq1) overexpression phenotype.

Expression of E(spl)m8-HLHEPC05-346 and phylScer\UAS.cPa under the control of Scer\GAL4Eq1 leads to missing external sensory organs.

Expression of esgEPA02-050 and phylScer\UAS.cPa under the control of Scer\GAL4Eq1 leads to missing external sensory organs.

Expression of CG10588EPC05-439 and phylScer\UAS.cPa under the control of Scer\GAL4Eq1 leads to missing external sensory organs.

Expression of dbrEPC05-544 and phylScer\UAS.cPa under the control of Scer\GAL4Eq1 leads to a disorganised external sensory organ pattern.

Co-expression of talScer\UAS.cPa and phylScer\UAS.cPa in the wing disc under the control of Scer\GAL4dpp.blk1 causes strong L3 vein expansion that is accompanied by ectopic external sensory organ formation.

Co-expression of talScer\UAS.cPa and phylScer\UAS.cPa under the control of Scer\GAL4dpp.blk1 induces approximately 7.4 (+/- 1.5) ectopic external sensory organs.

Co-expression of tal1-4FS.Scer\UAS does not enhance the phylScer\UAS.cPa ectopic external sensory organ phenotype (when both are expressed by Scer\GAL4dpp.blk1).

Co-expression of tal1-4FS.Scer\UAS and phylScer\UAS.cPa in the wing disc under the control of Scer\GAL4dpp.blk1 does not affect wing vein and external sensory organ formation.

Co-expression of talORF1.Scer\UAS with phylScer\UAS.cPa, both under the control of Scer\GAL4dpp.blk1, induces as many as 7.2 (+/- 1.4) ectopic external sensory organs.

Co-expression of talORF3.Scer\UAS with phylScer\UAS.cPa, both under the control of Scer\GAL4dpp.blk1, induces as many as 9.6 (+/- 2.5) ectopic external sensory organs.

Expression of talEPC05-660 and phylScer\UAS.cPa under the control of Scer\GAL4Eq1 leads to an increase in external sensory organ density (more than upon expression of phylScer\UAS.cPa alone).

Co-expression of talORF1.Scer\UAS with phylScer\UAS.cPa, both under the control of Scer\GAL4dpp.blk1, results in strong L3 wing vein expansion and formation of a large number of external sensory organs on the L3 vein.

Co-expression of talScer\UAS.cPa and phylScer\UAS.cPa under the control of Scer\GAL4Eq1 induces ectopic external sensory organs on the notum.

Most notal microchaetae are missing in animals coexpressing phylScer\UAS.cPa and ttkp69.Scer\UAS under the control of Scer\GAL4Eq1.

Xenogenetic Interactions
Statement
Reference
Complementation and Rescue Data
Comments
Images (0)
Mutant
Wild-type
Stocks (1)
Notes on Origin
Discoverer
External Crossreferences and Linkouts ( 0 )
Synonyms and Secondary IDs (3)
Reported As
Symbol Synonym
phylScer\UAS.cPa
phylUAS.cPa
Name Synonyms
Saccharomyces cerevisiae UAS construct a of Pi
Secondary FlyBase IDs
    References (5)