sV23, VM26A.2, fs(2)QJ42, TU-4
Please see the JBrowse view of Dmel\Vm26Ab 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
Gene model reviewed during 5.56
0.7 (northern blot)
168 (aa); 16.595 (kD predicted)
Interacts with vml and Vm26Aa; forms part of a disulfide-linked network within the vitelline membrane of stage 10 egg chambers.
Proteolytically processed after secretion into the perivitelline space (PubMed:15136154). Undergoes several proteolytic processing steps during formation of the vitelline membrane; an initial processing step removing a C-terminal propeptide occurs between stage 9 and 12 of oogenesis while a second removing a N-terminal propeptide occurs between stage 11 and 14 (PubMed:15136154, PubMed:20832396).
Becomes part of a disulfide-linked network including other vitelline membrane proteins, including vml and Vm26Aa, during vitelline membrane biogenesis and maturation (PubMed:20832396). Cys-123, Cys-131 and Cys-140 are involved in disulfide network formation, with Cys-131 being the most important (PubMed:20832396). Undergoes both disulfide and non-disulfide cross-linking upon incorporation into the vitelline membrane (PubMed:18514182).
The tetrapeptide (A-A-P-[AV]) repeats found throughout the protein are also present in many proteins constituting the protective envelope of other species.
The C-terminal propeptide is removed between stage 9 and 12 of oogenesis (PubMed:15136154). The C-terminal propeptide is non-essential for egg fertility (PubMed:15136154).
The N-terminal propeptide is removed between stage 11 and 14 of oogenesis (PubMed:15136154). The N-terminal propeptide is essential for egg fertility but its removal is not; may be involved in positioning and aligning this protein to facilitate disulfide and non-disulfide cross-linking within the vitelline membrane (PubMed:15136154).
The VM domain may be involved in facilitating efficient secretion of this protein.
Click to get a list of regulatory features (enhancers, TFBS, etc.) and gene disruptions (point mutations, indels, etc.) within or overlapping Dmel\Vm26Ab 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).
Vm26Ab is expressed by all oocyte-associated follicle cells.
JBrowse - Visual display of RNA-Seq signals
View Dmel\Vm26Ab in JBrowse2-18
2-19.2
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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.
In a sample of 79 genes with multiple introns, 33 showed significant heterogeneity in G+C content among introns of the same gene and significant positive correspondence between the intron and the third codon position G+C content within genes. These results are consistent with selection adding against preferred codons at the start of genes.
Polyclonal antibodies have been used to localise Vm26Aa, Vm26Ab, Cp18 and Cp36 in the assembly and mature eggshell. Vitelline membrane proteins are processed in a stage specific manner, morphological integrity of the outer chorion layers is dependent upon proper expression of at least one vitelline membrane component, sV23.
In situ hybridisation of recombinant DNA probes to polytene chromosomes of D.melanogaster and D.virilis is performed to study homologies between the chromosomal Muller elements of the two species.