ash-2
trithorax family member - component of the histone methyltransferase complex that specifically methylates lysine 4 of histone H3 - downregulating histone H1 hyperphosphorylation - depletion cause homeotic transformations and pattern-formation defects
Please see the JBrowse view of Dmel\ash2 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 5.44
Gene model reviewed during 5.49
2.0 (northern blot)
None of the polypeptides share 100% sequence identity.
94 (kD observed)
572 (aa); 64.8 (kD predicted)
Core component of several methyltransferase-containing complexes. Component of the SET1C/COMPASS complex, composed at least of the catalytic subunit Set1, wds/WDR5, Wdr82, Rbbp5, ash2, Cfp1/CXXC1, hcf and Dpy-30L1 (PubMed:21694722, PubMed:21875999). Component of the MLL3/4 (Histone-lysine N-methyltransferase/demethylase TRR) complex composed at least of the catalytic subunit trr, ash2, Rbbp5, Dpy-30L1, wds, hcf, ptip, Pa1, Utx, Lpt and Ncoa6 (PubMed:21875999). Interacts with hcf (PubMed:17466076). Interacts with trr (PubMed:23197473).
Click to get a list of regulatory features (enhancers, TFBS, etc.) and gene disruptions (point mutations, indels, etc.) within or overlapping Dmel\ash2 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
The ash2 transcript is present throughout development.
In Western blots, a 70 kD protein is detected in 2nd and 3rd instar larvae and a 53 kD protein is detected in pupae. The ash2 protein is detected in imaginal discs and in the nuclei of salivary gland and fat body cells.
JBrowse - Visual display of RNA-Seq signals
View Dmel\ash2 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.
polyclonal
DNA-protein interactions: genome-wide binding profile assayed for ash2 protein in Kc167 cells; see Chromatin_types_NKI collection report. Individual protein-binding experiments listed under "Samples" at GEO_GSE22069 (http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSE22069).
ash2 has a role in wing development.
Phenotypes of ash2 mutants that survive to the end of metamorphosis reveal that the ash2 gene product does not solely regulate homeotic selector genes. Pattern formation abnormalities are observed on mutant legs and wings. ash2 is a nuclear protein that is present in larval imaginal discs at a low level and at a much higher level in imaginal discs after puparium formation. The size of the ash2 protein changes dramatically at the end of the third larval instar suggesting that the protein has different functions in larvae than in pupae.
Mutations in ash2 give rise to homeotic transformations.
Genetic tests were used to confirm that ash1 and ash2 belong to a functionally related class of genes, mutations in which cause a wide variety of homeotic transformations that are similar to the transformations caused by trx. Double heterozygotes of ash2 alleles and Df(3R)red-P93 show a significant penetrance of homeotic transformations.
A member of the trithorax group of genes.
Most alleles homozygous lethal; stage of lethality variable. Surviving and pharate adults display transformations similar to those indicated for ash1. Homozygous lethal; labial and wing discs appear normal; eye-antenna, prothoracic, haltere, leg and genital discs homeotically transformed. Disc and cell autonomous.
Source for merge of: l(3)S112411 ash2
"ash2" mutations complement alleles of "aor".
Source for identity of: ash2 CG6677