Leucine-rich repeat transmembrane protein - along with Capricious, contributes to the adhesive properties of the cells in the morphogenetic furrow, thus regulating control of spacing ommatidial clusters - regulates boundary formation in the leg and wing -regulates tracheal branching
Please see the JBrowse view of Dmel\trn 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 5.44
Stop-codon suppression (UGA) postulated; FBrf0216884.
Gene model reviewed during 5.39
Low-frequency RNA-Seq exon junction(s) not annotated.
Gene model reviewed during 5.46
3.3 (northern blot)
None of the polypeptides share 100% sequence identity.
733 (aa)
Click to get a list of regulatory features (enhancers, TFBS, etc.) and gene disruptions (point mutations, indels, etc.) within or overlapping Dmel\trn using the Feature Mapper tool.
Comment: anlage in statu nascendi
Comment: anlage in statu nascendi
Comment: anlage in statu nascendi
Comment: reported as ventral nerve cord 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
Comment: reported as dorsal epidermis anlage
trn transcripts are detected at all stages of development on northern blots with a peak in 3-12hr embryos. By in situ hybridization, they are first detected at embryonic stage 5 in 8 transverse stripes, the seven most posterior of which correspond to the even pair-rule stripes. At stage 8, four longitudinal trn-expressing stripes appear in the ventrolateral region of the embryo. These coincide with the medial and lateral columns of ac expression. At this time, trn is also expressed in patches of cells on the head that will probably give rise to the brain and anterior sense organs. From stage 8 on, a complex and dynamic pattern of expression is observed involving lateral and longitudinal stripes. From stage 9 on, expression is observed in developing PNS cells including the ventral, lateral, and dorsal sense organs. During stages 15 and 16, trn expression is observed transiently in the stomodeum, proctodeum, and in a short region of the hindgut. In stages 16 and 17 expression is observed in the CNS. During larval and pupal stages, trn expression is associated with the developing CNS and PNS. In third instar larval leg, wing, and eye-antennal discs, regions of trn expression coincide with positions of developing sense organs as well as the inner and outer proliferation centers of the optic lobe. In the eye disc, trn transcripts are found in a repeating pattern at the anterior edge of the morphogenetic furrow and in a subset of developing photoreceptor cells posterior to the furrow.
GBrowse - Visual display of RNA-Seq signals
View Dmel\trn in GBrowse 23-40
3-34.2
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 GBrowse 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.
Source for merge of: trn anon- EST:fe2B1
The extracellular domain of the trn protein is sufficient for its role in the formation of tracheal branches.
trn protein confers affinity for dorsal cells during wing development.
Candidate gene for quantitative trait (QTL) locus determining bristle number.
The primary target genes of Egfr are pnt, vnd and Fas3, these are induced in different ectodermal domains. Secondary target genes oc, argos and trn are activated by pnt in response to Egfr signalling. The proper induction of these genes requires the concomitant inactivation of aop, mediated by Egfr signalling.