neu, Neuralised
cytoplasmic zinc finger signaling protein - neurogenic - promotes or modulates the Notch neurogenic signal at the receptor/ligand level
Please see the JBrowse view of Dmel\neur 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 5.48
Gene model reviewed during 5.55
4.1, 3.7 (northern blot)
4.2, 4.0 (northern blot)
753 (aa)
754 (aa); 82 (kD predicted)
411 (aa)
last few amino acids differ from neur+P754
Click to get a list of regulatory features (enhancers, TFBS, etc.) and gene disruptions (point mutations, indels, etc.) within or overlapping Dmel\neur 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: anlage in statu nascendi
Comment: anlage in statu nascendi
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: 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: reference states 3-9 hr AEL
Comment: reference states 3-9 hr AEL
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
Comment: reference states 0-12 hr AEL
Expression pattern inferred from unspecified enhancer trap line.
neur expression is undetectable before late third instar, and is first observed in the sensory organ precursors of the wing disc.
The protein can be detected at the plasma membrane and in many intracellular vesicles in eye disc photoreceptors.
JBrowse - Visual display of RNA-Seq signals
View Dmel\neur in JBrowse





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.
neur overexpression in the mushroom bodies enhances long-term memory but not anaesthesia-resistant memory.
Expression is enriched in embryonic gonads.
neur is required for both germline stem cell maintenance and gonial cell viability.
dsRNA made from templates generated with primers directed against this gene tested in RNAi screen for effects on Kc167 and S2R+ cell morphology.
neur is required for the socket/shaft and neuron/sheath fate decisions and acts in the pIIb cell to specify the pIIa cell.
neur has a role in the reception of the lateral inhibitory signal during peripheral neurogenesis.
The RING finger domain of neur acts as an E3 ubiquitin ligase in vitro.
Mosaic analysis demonstrates that neur is required in a cell autonomous manner for the selection of the sensory organ precursor from the proneural cluster for the determination of the sensory organ precursor progeny cell fates.
Mutation in neur affects sensory organ precursor formation.
neur is required for PNS development in the embryo.
Comparison of D.melanogaster and D.virilis show that it is possible to identify key functional regions of the neur protein by interspecific comparison.
Molecular analysis of neur indicates a DNA binding function for the gene product.
The embryonic phenotype of neurogenic mutations was examined in most tissues using Ecol\lacZ enhancer trap lines. All alleles examined show defects in many organs from all three germ layers. At least for ectodermally and endodermally derived tissues, neurogenic gene function is primarily involved in interactions among cells that need to acquire or maintain an epithelial phenotype.
Ecol\lacZ reporter gene constructs demonstrate that neurogenic loci are required to restrict the number of competent cells that will become sensory mother cells, SMCs.
Neural hyperplasia, caused by mutations in neu, can be prevented by the presence of another neurogenic mutation.
neu mutants display no ventral cuticle and hypertrophy of the central nervous system.
Source for merge of: neur BEST:LD21494