Su(Raf)2C, phy1
a target of EGFR signalling in the eye - protein degradation cofactor - involved in a negative cross talk between RTK and Notch/Wg pathways - Post‐transcriptional downregulation of Notch and Wg signalling by Phyl allows fine‐tuning of the signal and creates a delicate balance between active signalling of Notch/Wg pathways and their degradation by the lysosomal pathway
Please see the JBrowse view of Dmel\phyl 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 5.50
1.8 (northern blot)
There is only one protein coding transcript and one polypeptide associated with this gene
400 (aa)
400 (aa); 45 (kD predicted)
Component of some E3 complex at least composed of sina, ebi and phyl, required for the degradation of ttk.
Click to get a list of regulatory features (enhancers, TFBS, etc.) and gene disruptions (point mutations, indels, etc.) within or overlapping Dmel\phyl 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: anlage in statu nascendi
Comment: reported as procephalic ectoderm anlage in statu nascendi
Comment: reported as procephalic ectoderm anlage in statu nascendi
Comment: reported as procephalic ectoderm anlage in statu nascendi
Comment: reported as procephalic ectoderm anlage
Comment: reported as procephalic ectoderm anlage
Comment: reported as procephalic ectoderm anlage
Comment: reported as procephalic ectoderm anlage
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
phyl transcripts are expressed in the eye imaginal disc. They are first expressed in a periodic group of cells in the morphogenetic furrow and are later expressed in a dynamic pattern in a subset of photoreceptor cells. The staining intensity is reduced immediately posterior to the furrow and becomes more intense again approximately six rows behind the furrow. Perinuclear staining becomes evident in photoreceptor cells R1 and R6 in row 6. By row 7, perinuclear staining is evident in R7. Staining remains strong in R1, R6, and R7 through row 9 and then diminishes. None of the other photoreceptor cells or the cone cells express phyl.
phyl transcripts are expressed in a highly dynamic pattern in the eye imaginal disc. Within the morphogenetic furrow, they are detected in regularly spaced clusters of about 12 cells. Posterior to the furrow, they are mostly confined to a thin stripe approximately spanning the region between ommatidial columns 4-8. Within this stripe, phyl transcripts appear in clusters that appear to consist of three cells, presumed to be the precursors of photoreceptor cells R1, R6, and R7. No transcripts are detected in cone cell precursors.
JBrowse - Visual display of RNA-Seq signals
View Dmel\phyl in JBrowse



2-71
2-75.6
2-
2-70.3
2-73.0 +/- 0.7
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.
phyl is required for the formation of sensory organ precursor cells (SOPs) and cell fate specification of SOP progeny.
Identified in a genetic screen for modifiers of the phl::tor12D.sev rough eye mutant phenotype.
phyl encodes a novel protein autonomously required for fate determination of photoreceptors R1, R6 and R7. Genetic data suggest phyl acts downstream of Ras85D, phl and aop to promote neuronal differentiation in R1, R6 and R7. Ectopic expression of phyl in the cone cell precursors mimics the effect of ectopic activation of Ras85D suggesting that phyl expression is regulated by Ras85D. phyl expression is also required for embryonic nervous system and sensory bristle development.
Required for photoreceptor differentiation, acting downstream of Ras.
The phyl gene regulates the fates of a subset of cells in the developing eye and represents a possible target gene of the Raf pathway. Within photoreceptors R1, R6 and R7, phyl expression mimics the activation of the Raf pathway in its ability to induce photoreceptor rather than cone cell development. The transformation of cone cells into R7 cells in response to Raf activation is accompanied by and dependent upon ectopic phyl expression.
The name "phyl" ("phyllopod") was inspired by the phenotype of homozygous phyl clones in the eye. In such clones five photoreceptors and 5-6 cone cells are present, resembling the compound eye of some phyllopods (class Crustacea).
The phyl mutants cause an ommatidial composition similar, but not identical to that of some phyllopod crustacea, such as Leptodora, hence the gene name.