ming, l(3)neo33
transcription factor - zinc finger - temporal network regulator the development of late CNS sublineages - a genetic cascade involving klumpfuss, nab and castor specifies the abdominal leucokinergic neurons in the Drosophila CNS - Pdm and Castor close successive temporal identity windows in the NB3-1 lineage - triggers genes in a specific lineage that act to sub-divide the broader Cas window
Please see the JBrowse view of Dmel\cas for information on other features
To submit a correction to a gene model please use the Contact FlyBase form
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 5.47
Gene model reviewed during 5.49
3.3 (northern blot)
3.7 (northern blot)
None of the polypeptides share 100% sequence identity.
799 (aa); 88 (kD)
Click to get a list of regulatory features (enhancers, TFBS, etc.) and gene disruptions (point mutations, indels, etc.) within or overlapping Dmel\cas 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: anlage in statu nascendi
Comment: anlage in statu nascendi
Comment: reported as procephalic ectoderm anlage
Comment: reported as procephalic ectoderm anlage
Comment: reported as procephalic ectoderm anlage
Comment: reported as procephalic ectoderm anlage
Comment: reported as ventral nerve cord anlage
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
cas transcripts are first detected at stage 9 in a subset of midline cells. Slightly later, one neuroblast in every hemisegment expresses cas. By late stage 11, cas transcripts are expressed in 17 identified neuroblasts in every hemisegment of the CNS. Transcript levels decrease by stage 14 and are undetectable by stage 16. Transcripts are detected only in midline cells, ganglion mother cells and neuroblasts and not in the neurogenic ectoderm or neurons.
The highest levels of cas mRNA expression coincide with embryonic CNS development but low levels can be detected in third instar larvae and adults. Expression occurs in a restricted set of neuroblasts and glia in the cephalic regions and the ventral nerve cord. Expression is seen in both the lateral CNS and the midline and the midline expression shows an anterior to posterior gradient.
Comment: in 10-50% of examined hemisegments
Comment: in 10-50% of examined hemisegments
Comment: in 10-50% of examined hemisegments
Comment: in 10-50% of examined hemisegments
cas protein is expressed in follicle stem cells, interfollicle (stalk) cells, and polar follicle cells, but not oocyte associated (main body) follicle cells.
cas protein is expressed during oogenesis in prefollicle cells, and in interfollicle (stalk) cells, and polar follicle cells.
Neuroblast NB3-3 produces a series of interneurons, including a cluster of 11 eve-positive interneurons (the Eve-lateral or EL neurons). Kr is expressed at the first division of NB3-3 and specifies an eve-negative interneuron, followed by production of the 11 EL neurons, six of which are at least partially specified by cas.
cas is expressed in the NB5-6 lineage in thoracic and abdominal segments and in all more anterior segments in a late temporal window.
cas is seen to be expressed in two waves in the thoracic neuroblast NB3-3, not being detected in late embryonic stage 13 to late embryonic stage 14. However, in the abdominal neuroblast NB3-3 the first wave ends earlier (end of stage 12), and the second wave both begins and ends earlier (late stage 13 to early stage 14).
Expression assayed at stages 9, 11, 13, and 17. Expression may be continuous between assayed stages in some tissues.
Expression in procephalic neuroblasts stage 9-11: tritocerebrum - d2, d4, v4; deuterocerebrum - d1, d2, d4-7,v3, v6-8; protocerebrum - ad5, ad6, ad8-11, ad13, ad16-18, av1, cd2-4, cd6-8, cd10-21, cv1-4, cv6-9, pd1-14, pd17-19, pv1, pv3
In larvae, cas is expressed in disseminated cells on the ventral side of the VNC. On the dorsal side of the third instar larval brain, cas is expressed in five linearly organised cell clusters on both sides of the interhemispheric junction. Expression of cas gradually disappears from the CNS during pupation, and no clear signal is seen in adult brain.
Comment: late stage 11
Comment: late stage 11
Comment: late stage 11
Comment: late stage 11
Comment: late stage 11
Comment: late stage 11
Comment: late stage 11
Comment: late stage 11
Comment: late stage 11
JBrowse - Visual display of RNA-Seq signals
View Dmel\cas in JBrowse3-47.5
3-44.1
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.
polyclonal
cas is involved in post-embryonic brain development.
The embryonic CNS contains sequentially generated neuroblast sublineages that can be distinguished by their expression of either hb, nub or cas. hb and cas may directly silence nub expression in early and late developing sublineages, given that nub cis-regulatory DNA contains approximately 32 hb/cas-binding sites and its enhancer(s) are ectopically activated in cas- neuroblasts. Targeted misexpression of cas in all neuronal lineages reduces nub expression without altering hb expression. By ensuring correct POU gene expression boundaries hb and cas maintain temporal subdivisions in the cell-identity circuitry controlling CNS development.
cas, eve, unpg and ac are expressed in specific neuroblast sublineages. Expression studies using pbl and stg mutants suggest that neuroblasts have an intrinsic gene regulatory hierarchy controlling unpg and ac expression but that cell cycle- or cytokinesis-dependent mechanisms are required for cas and eve CNS expression.
cas was identified by an enhancer trap insertion expressed in a subset of neuroblasts at reproducible points in their cell lineage, and is proposed to control cell fate within neuroblast cell lineages. cas is required for the correct CNS expression of engrailed, and loss of cas function results in precise alterations in CNS gene expression, defects in axonogenesis and embryonic lethality.
Expression analysed in CNS study of neuroblasts and ganglion mother cells, using an enhancer trap to reveal the expression pattern.
cas encodes a putative transcription factor whose expression is required for normal development of a subset of neuronal precursors.
castor mutations cause loss of axonal density & aberrant engrailed expression late in CNS development.
Source for merge of: cas l(3)neo33
Source for merge of: cas CG2102
"ming" means "fate" in Chinese.
"plx" ("pollux") and "cas" ("castor") are named after the Greek mythological brothers due to their close apposition.