H4r
Please see the JBrowse view of Dmel\His4r 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
Annotated transcripts do not represent all supported alternative splices within 5' UTR.
Gene model reviewed during 5.55
Low-frequency RNA-Seq exon junction(s) not annotated.
The nucleosome is a histone octamer containing two molecules each of H2A, H2B, H3 and H4 assembled in one H3-H4 heterotetramer and two H2A-H2B heterodimers. The octamer wraps approximately 147 bp of DNA. Interacts with Nasp; the interaction is probably indirect, mediated by histone H3 (PubMed:36930688). Interacts with Parp1 (via C-terminus); the interaction is direct and regulates Parp1 enzymatic activity (PubMed:17827147, PubMed:24508391).
Acetylated on Lys-6 (H4K5ac) and Lys-13 (H4K12ac) during prophase I of meiosis. Phosphorylation of H2A 'Thr-119' is a prerequisite for H4 Lys-6 acetylation but not for H4 Lys-13 acetylation (PubMed:16230526, PubMed:18327897). Acetylated on Lys-6 and Lys-13 by the Ada2a-containing (ATAC) histone acetyltransferase complex (PubMed:22796493).
The N-terminal tail is essential for nucleosome dependent activation of Parp1.
Click to get a list of regulatory features (enhancers, TFBS, etc.) and gene disruptions (point mutations, indels, etc.) within or overlapping Dmel\His4r 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).
JBrowse - Visual display of RNA-Seq signals
View Dmel\His4r 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.
RNAi generated by PCR using primers directed to this gene causes a cell growth and viability phenotype when assayed in Kc167 and S2R+ cells.
Identification and characterisation of histone H4 replacement genes from D.melanogaster and D.hydei.
Source for merge of: His4r BcDNA:RH52884
Source for merge of His4r BcDNA:RH52884 was a shared cDNA ( date:030728 ).