dARNT, ARNT, HIF-1, jaywalker, Hif1
Myc-type, helix loop helix and PAS family protein - Tango heterodimerizes with two transcription factors, Trachealess and Single minded, to regulate transcription in the trachea and central midline, respectively
Please see the JBrowse view of Dmel\tgo 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.
Low-frequency RNA-Seq exon junction(s) not annotated.
Gene model reviewed during 5.48
2.355 (longest cDNA)
2.620 (longest cDNA)
3.079 (longest cDNA)
Efficient DNA binding requires dimerization with another bHLH protein. Heterodimer with ahr, trh or sim.
Click to get a list of regulatory features (enhancers, TFBS, etc.) and gene disruptions (point mutations, indels, etc.) within or overlapping Dmel\tgo 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: maternally deposited
Comment: reference states transcript expressed up to 8-12 hr AEL
In addition to the midline and tracheal expression, tgo is expressed in the antennal segment, the gnathal segments, the leg anlage, and the PNS in embryos.
tgo is ubiquitously distributed in early embryos. Strong signals are transiently detected in tracheal pits at stage 11. Later, strong expression is observed in the CNS.
tgo is ubiquitously expressed during embryogenesis. Elevated levels were observed in tracheal placodes and tracheal pits.
tgo expression was detected in oocytes and embyros up to 8-12 hr of development.
In embryos, in addition to the midline and tracheal expression, tgo is expressed in the antennal segment, the gnathal segments, the leg anlage, the PNS, and the dorsal vessel.
tgo is uniformly distributed in preblastoderm embryos. During the extended germ band stage, tgo protein is found in all three germ layers. Enhanced levels of tgo protein are found around the forming tracheal pits. Enhanced levels of tgo protein continue to be observed in tracheal cells including the posterior spiracles from stage 11 to 17. Enhanced levels are also observed in the supraoesophageal ganglion and the ventral nerve cord.
JBrowse - Visual display of RNA-Seq signals
View Dmel\tgo in JBrowse3-48
3-45.8
3-44 +/- 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 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.
monoclonal
New stable cell line derived from S2-unspecified : 75 stable S2 cell lines containing a library of intrinsically disordered regions (IDRs) fluorescently tagged with mNeonGreen were constructed. In addition, stable S2 cell lines expressing the following full-length transcription factors were generated: da, rib, CG10321, CG13287, tgo, Spps, CG31510, brk, and disco.
tgo has a cell-autonomous function in the peripheral glia.
dsRNA has been made from templates generated with primers directed against this gene. RNAi of tgo results in reduced arborization of ddaD and ddaE neurons, defects in muscle, alterations in the number of MD neurons, defects in dendrite morphogenesis. However, RNAi causes no obvious defects in da dendrite development.
Two EMS induced alleles were identified in a screen for mutations affecting commissure formation in the CNS of the embryo.
tgo has been cloned and sequenced. Isolated form an embryonic cDNA library using a human hARNT cDNA as a probe.
sim and trh activate transcription by forming dimers with the tgo protein. Gene dosage studies reveal in vivo interactions between sim and tgo, and trh and tgo. The interacting proteins in vivo control CNS midline and tracheal transcription and development. tgo protein is found broadly distributed throughout embryogenesis, although certain cell types, including trachea and the CNS have enhanced levels.
Mutants cause CNS and tracheal defects.
Mutation in jay affects neuronal connections, affecting pathway finding.
jay is required for PNS development in the embryo.
Source for merge of: tgo jay