Toll-2, Toll2, tlr, EP-709
transmembrane - leucine-rich repeat motif (LRR) - a critical component of the humoral immune response
Please see the JBrowse view of Dmel\18w 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 5.46
5.6 (northern blot)
There is only one protein coding transcript and one polypeptide associated with this gene
1385 (aa)
1389 (aa); 155 (kD predicted)
Click to get a list of regulatory features (enhancers, TFBS, etc.) and gene disruptions (point mutations, indels, etc.) within or overlapping Dmel\18w 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 anlage in statu nascendi
Comment: reported as procephalic ectoderm anlage in statu nascendi
Comment: reported as procephalic ectoderm anlage in statu nascendi
Comment: anlage in statu nascendi
Comment: reported as dorsal epidermis anlage
Comment: reported as head epidermis primordium
Comment: reported as head epidermis primordium
Comment: reported as head epidermis primordium
Comment: during invagination
18w transcript is expressed in the proximal region of the wing disc, and the anterior compartment in leg discs; expression is absent from the wing pouch.
18w is expressed before and throughout salivary gland invagination during embryonic stages 11 and 12. At stage 13, it is no longer expressed in the salivary glands but is detected in salivary gland ducts.
18w is expressed in follicle cells from oogenesis stage 8 until the end of oogenesis. From stage 8 to 10A, 18w accumulates in the main body follicle cells but not in the terminal cells. Expression is also detected in stalk cells. Later, as the main body follicle cells migrate posteriorly over the oocyte, they continue to express 18w, but expression is not detected in the squamous follicle cells left covering the nurse cells. By stage 10B, expression is limited to a large patch of cells on the dorsal anterior side of the oocyte and to the centripetally migrating cells. During stage 11, the pattern is refined to the centripetally migrating cells and anterior cells along the dorsal midline. Expression remains high in cells secreting the collar and in some of the cells that secrete the dorsal appendages that may be the floor-forming cells of the dorsal appendages.
18w expression is enriched in centripetal cells relative to other cells in the egg chamber.
18w transcripts are detected at all stages of development.
18w is expressed in all developmental stages tested. Expression is first observed at the syncytial blastoderm stage in the presumptive hindgut, head regions, and parasegment 2. Shortly after, stripes of expression are seen first in the even numbered parasegments and then in the odd numbered parasegments. By the extended germ band stage, 18w is expressed in 15 transverse stripes with patches of expression corresponding to the 4 head segments and the hindgut as well. 18w expression in the trunk region was shown to overlap the wg and en stripes and spans the parasegmental boundary. At full germ band extension, the stripes begin to fade and expression is observed in segmentally repeated lateral clusters corresponding to the tracheal pits and the segmental grooves. Expression is accentuated in the cells surrounding the anterior and posterior spiracles. Transient expression in the CNS is also seen. Later, 18w expression is observed in the wing and haltere disc primordia, the dorsal vessel, the antennal-maxillary sense organs, the clypeolabrum, the anterior and posterior spiracles, and in the anal plate.
18w transcripts are expressed in all stages of development tested. They are expressed in a complex pattern during embryogenesis. Expression is first observed just prior to cellular blastoderm formation in three stripes in the anterior portion of the embryo and a broader posterior domain. Subsequently, stripes are seen in the central region of the embryo. At late cellular blastoderm, secondary stripes appear leading to the transient expression of 18 stripes during early gastrulation and 20 stripes at stage 10. 18w expression overlaps the wg and en stripes and spans the parasegmental boundary. At maximum germ band extension, expression is observed along the ventral midline in small clusters of cells posterior to each stripe. Staining is also observed in salivary gland placodes, in tracheal pits, and in five areas in the presumptive head region. During germ band retraction, transcripts are less abundant and more restricted. They are observed in the developing tracheal system, the salivary gland anlagen, the anlagen for the anal plate, the posterior spiracles, the clypeolabrum, and in cells that participate in the formation of the dorsal vessel. In stage 15 and 16, 18w expression is also observed in regions of the head, pharynx, stomach, and hindgut.
JBrowse - Visual display of RNA-Seq signals
View Dmel\18w in JBrowse2-90
2-95.6
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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
dsRNA has been made from templates generated with primers directed against this gene.
Loss of function 18w mutant follicle cells exhibit delayed migration. The eggs laid by feamles with ovarian clones show defects in egg shape and dorsal appendage morphology.
Mutant allele fails to complement a QTL affecting male mating behaviour.
dsRNA made from templates generated with primers directed against this gene tested in RNAi screen for effects on Kc167 and S2R+ cell morphology.
18w is a critical component of the humoral immune response.
18w protein is 1389 amino aids in length.
The 18w protein functions as a receptor mediating intercellular communication during various developmental events, including pattern formation, imaginal cell determination and the larval immune response. Expression of 18w protein in non-adhesive Schneider 2 cells promotes heterophilic cell aggregation as seen in similar experiments with Tl and other receptor-ligand molecules.
Molecular and phenotypic analysis suggests 18w participates in the developmental program specified by segmentation and homeotic genes as a cell adhesion or receptor molecule that facilitates cell movements.
Source for merge of: 18w EP-709
Source for identity of: 18w CG8896
Named "18 wheeler" on basis of 18 stripes of expression during early gastrulation.