l(2)k07918, l(2)ft, l(2)79/18, l(2)fat, CT11259
cadherin domain transmembrane receptor that negatively controls cell proliferation - also functions in planar polarity - Fat functions in the Hippo signaling pathway and the Dachsous-Fat planar cell polarity pathway
Please see the JBrowse view of Dmel\ft for information on other features
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AlphaFold produces a per-residue confidence score (pLDDT) between 0 and 100. Some regions with low pLDDT may be unstructured in isolation.
Gene model reviewed during 5.45
15-20 Kb (northern blot)
There is only one protein coding transcript and one polypeptide associated with this gene
5147 (aa); 560 (kD)
Interacts with Fbxl7 (PubMed:25107277). Ft-mito interacts with NADH dehydrogenase subunit ND-24 and with ATP synthase subunit ATPsynC (PubMed:25215488).
Phosphorylated by fj on Ser/Thr of cadherin domains (PubMed:18635802). Phosphorylation by fj enhances binding to ds (PubMed:20434335). Phosphorylated in the cytoplasmic domain in a dco-dependent manner which is promoted by ds (PubMed:19574458).
Proteolytically cleaved to yield stably associated N- and C-terminal fragments (PubMed:19574458). The C-terminal fragment is processed further to release a 68 kDa mitochondrial fragment, Ft-mito (PubMed:25215488).
The extracellular domain is required for correct subcellular localization and for cell adhesion.
The intracellular domain is sufficient for viability, growth control and planar cell polarity.
Click to get a list of regulatory features (enhancers, TFBS, etc.) and gene disruptions (point mutations, indels, etc.) within or overlapping Dmel\ft using the Feature Mapper tool.
The testis specificity index was calculated from modENCODE tissue expression data by Vedelek et al., 2018 to indicate the degree of testis enrichment compared to other tissues. Scores range from -2.52 (underrepresented) to 5.2 (very high testis bias).
Comment: reported as procephalic ectoderm primordium
Comment: reported as procephalic ectoderm primordium
Comment: reported as procephalic ectoderm primordium
Comment: reported as procephalic ectoderm primordium
Comment: reported as procephalic ectoderm primordium
Comment: reported as procephalic ectoderm primordium
Comment: reported as head epidermis primordium
Comment: reported as head epidermis primordium
Comment: reported as head epidermis primordium
ft transcripts are first detected at stage 7 of embryogenesis in the surface ectoderm and in some ectodermal derivatives. Later they are seen in the pharyngeal region of the foregut and in the hindgut. In larvae, ft transcripts are expressed in a small set of neurons in the optic lobes and uniformly in all imaginal discs.
Comment: at the border
Comment: at the border
Comment: at the border
Comment: at the border
Comment: at the border
Comment: at the border
ft protein is expressed strongly both in larval and pupal stages at the borders or the secondary and tertiary pigment cells, the bristle cells, and the four cone cells.
JBrowse - Visual display of RNA-Seq signals
View Dmel\ft in JBrowse



2-11
2-12.2
2-12.0
2-10.4 +/- 2.5
2-10.4 (Jurgens).
Please Note FlyBase no longer curates genomic clone accessions so this list may not be complete
Please Note This section lists cDNAs and ESTs that fall within the genomic extent of the gene model, which may include cDNAs and ESTs of genes within introns, or of overlapping genes. Please see JBrowse for alignment of the cDNAs and ESTs to the gene model.
For each fully sequenced cDNA the DGRC maintains various forms of the cDNA (e.g tagged or untagged) in several different host vectors for subsequent cloning and expression in Drosophila and Drosophila cell lines.
polyclonal
Cells lacking ft spend roughly equal proportions of time in the G1, S, and G2 phases of the cell cycle as wild-type cells
The extracellular domain of the ft product is not required for its activity in growth, planar cell polarity and proximodistal wing patterning.
dsRNA made from templates generated with primers directed against this gene tested in RNAi screen for effects on Kc167 and S2R+ cell morphology.
ft play an important role in the regulation planar polarity in the compound eye.
Mutants isolated in a screen of the second chromosome identifying genes affecting disc morphology.
Some of the proteins of apico-lateral junctions are required both for apico-basal cell polarity and for the signalling mechanisms controlling cell proliferation, whereas others are required more specifically in cell-cell signalling.
Mutants display hyperplastic phenotype, with imaginal disc overgrowth.
Endocrine mechanisms responsible for the prolongation of larval life in ft mutants were investigated: results suggest that delayed pupariation is caused by the overgrown imaginal discs inhibiting the production or release of ecdysteroids from the endocrine system.
Genetic and developmental characteristics of the imaginal disc overgrowth mutant have been determined. Mutants display hyperplastic phenotype, with imaginal disc overgrowth.
Mutant alleles display a range of phenotypes that disrupt imaginal disc development in a way that would be expected from defects in cell adhesion. Clones of cells homozygous for recessive lethal mutations show hyperplastic autonomous overgrowth, large patches of mutant tissue protrude from body surface, surrounding tissue is unaffected.
Mutants at ft exhibit hyperplastic overgrowth.
Located in the cytological interval 24D5-24D7 by deficiency mapping.
Viable alleles characterized using ft1. Abdomen short and fat. Thorax broad. Wings short and broad with crossveins much closer together than normal. Scutellum shortened; scutellar bristles far apart. Viability good. Second- and third instar larvae, particularly when there is little yeast in the food, show vacuoles in cytoplasm of salivary gland cells. Two waves of vacuole formation; vacuoles may be membrane-bound lipoprotein bodies (Chandhuri, 1969). Lethal alleles characterized in study of ft8 (formerly fd = floppy disc) by Bryant, Huettner, Held, Ryerse and Szidonya (1988). ft8 classified as an amorphic mutation based on the similarity in lethal phenotype of ft8/ft8 and ft8/Df(2L)M24F11. Larvae characterized by imaginal-disc hyperplasia such that mutant discs are much larger and more convoluted than wild type; the disc remains a single epithelial layer but in the highly convoluted proximal regions, of the wing disc at least, the columnar cells give way to cuboidal epithelial cells, which are deficient in cytoskeletal elements. Pupariation is delayed 3.2 days in mutants and the discs contain 122,000 cells at the end of nine days compared to 50,000 cells in wild type discs, which attain full growth at 5 days. Disc phenotype autonomous in transplants into adult hosts. Occasional mutant pupae reach the pharate-adult stage so that adult structures can be studied. Abdomens normal; eyes often swollen and may be split into two parts; extra head bristles; distal parts of antennae and legs may be missing; wings often fail to evaginate. Legs most severely affected; joints short and thick; missing tarsal joints and claws and tarsal fusions; increased bristle densities with deviant chaetal polarities; frequent outgrowths and ingrowths of cuticle; the latter giving rise to cuticle bound vesicles within the legs.