anillin, Ani, l(2)43Ec
encodes anillin - conserved component of the contractile ring that is essential for cytokinesis - physically interacts with three conserved cleavage furrow proteins, F-actin, myosin II and septins - required for 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.
Low-frequency RNA-Seq exon junction(s) not annotated.
Gene model reviewed during 5.48
4.3 (northern blot)
None of the polypeptides share 100% sequence identity.
1201 (aa); 190 (kD observed); 132 (kD predicted)
Interacts with and bundles F-actin.
Click to get a list of regulatory features (enhancers, TFBS, etc.) and gene disruptions (point mutations, indels, etc.) within or overlapping Dmel\scra 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: 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
scra protein is localized to the cytoskeleton during syncytial stage embryos. In dividing cells, the protein is localized in the nucleus during interphase. At nuclear breakdown, it becomes cytoplasmic and moves to the actin filaments in the cortex. During anaphase and telophase, it becomes highly enriched in the cleavage furrow along with myosin II. It is also found in metaphase furrows and nascent ring canals where it remains bound to the invaginated cortex. It is not expressed in cells that have left the cell cycle.
In S2 cells the scraprotein is found in a diffuse cortical pattern during methaphase but concentrates first in a broad equatorial band in anaphase then at the contractile ring throughout telophase.
scra protein is localized to the cellularization front, where it is required for microfilament ring formation during cellularization of the embryo.
scra protein expression is detected at all developmental stages with the highest levels in early to mid embryos.
JBrowse - Visual display of RNA-Seq signals
View Dmel\scra in JBrowse2-56.7
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.
New stable cell line derived from S2-unspecified : A scra- FBto0000118:mCherry S2 cell line was used.
New stable cell line derived from S2-unspecified : S2 cell lines coexpresing scra-GFP and wild type or kinase-dead versions of sti were generated.
New stable cell line derived from S2-unspecified : Stable S2 cell lines expressing scra-GFP were generated.
scra is required for the unequal cell divisions of the pIIb and pIIIb neuronal precursor cells, but not for the equal cell divisions of the lineage related precursor cells, during peripheral nervous system development in the embryo.
Expression is enriched in embryonic gonads.
dsRNA has made from templates generated with primers directed against this gene and transfected into Kc167 cells. More than 50% of these cells become multinucleate, suggesting a defect in cytokinesis.
dsRNA directed against this gene causes defects in cytokinesis when tested in an RNAi screen in S2 cells.
scra plays a role in the cytoskeletal dynamics that occur during cellularization of the blastoderm.
dsRNA made from templates generated with primers directed against this gene tested in RNAi screen for effects on Kc167 and S2R+ cell morphology.
RNAi screen using dsRNA made from templates generated with primers directed against this gene causes a phenotype when assayed in Kc167 and S2R+ cells: binucleate cells.
dsRNA made from templates generated with primers directed against this gene is tested in an RNAi screen for effects on actin-based lamella formation.
scra has been cloned and sequenced, and its expression pattern has been analysed.
Mutants exhibit an increase in neuronal cell size, it is possible l(2)k08255 plays a role in cell division.
Mutations in scra result in a maternal effect phenotype with defects during cellularisation of the blastoderm.
Source for merge of: scra Ani
Source for merge of: scra l(2)k08255
Source for identity of: scra CG2092
The gene is named "Anillin" (from the Spanish "anillo", for ring) based on the ring-shaped distribution of the protein in dividing cells.