wdo
novel protein that is essential for polarized growth of the plasma membrane during cellularization
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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 5.51
Gene model reviewed during 5.55
1196 (aa); 135 (kD)
Click to get a list of regulatory features (enhancers, TFBS, etc.) and gene disruptions (point mutations, indels, etc.) within or overlapping Dmel\slam 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: NOT germline cell
slam RNA and protein colocalize and mark the basal region of the cellularization furrow in early embryos. A 10-fold upregulation of slam transcript levels was measured at cellularization by quantitative PCR. A strong (6-fold) up-reulation of slam RNA is observed within a few minutes at the transition from mitosis 13 to interphase 14. RNA levels gradually decrease after 30 minutes during the second half of cellularization.
slam is expressed in all somatic cells of the blastoderm embryo, but is excluded from germline cells.
Transcript is first detected at embryonic cycle 13 and remains detectable through the slow phase of cellularization. The transcript disappears during the fast phase of cellularization and is no longer detectable at gastrulation.
Comment: NOT germline cell
slam RNA and protein colocalize and mark the basal region of the cellularization furrow in early embryos. slam protein levels peak at cellularization. A strong (6-fold) up-reulation of slam protein levels is observed within a few minutes at the transition from mitosis 13 to interphase 14. Protein levels remain constant in the second half of cellularization.
slam is expressed in all somatic cells of the blastoderm embryo, but is excluded from germline cells.
Protein is detected in discrete puncta in the cytoplasm and is first detected in the furrow canal region on the membrane of cellularizing embryos. slam protein can also be detected on the adjacent lateral membrane but not apically.
JBrowse - Visual display of RNA-Seq signals
View Dmel\slam in JBrowsePlease 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.
slam is necessary for polarised growth of membranes during cellularisation.
slam is required for cellularisation and for germ cell migration in the embryo.
slam controls a key aspect of membrane trafficking in membrane invagination that takes place during embryo cellularization.
In slam mutant embryos, the lateral transfer of apical membrane that normally takes place as new membrane is apically inserted is blocked. In addition, the Nrt protein is normally exported from the Golgi but accumulates in an apical compartment instead of being inserted into the recipient apical membrane.
Germ cells initiate migration by moving to the interior of the embryo through the posterior midgut epithelium in slam mutant embryos, but they are unable to orient properly on the midgut and subsequently fail to proceed along the correct migratory course.
Source for merge of: slam wdo CG9506