Statements in which the resource exists as a subject.
PredicateObject
rdf:type
biopax3:comment
FUNCTION: Core component of nucleosome. Nucleosomes wrap and compact DNA into chromatin, limiting DNA accessibility to the cellular machineries which require DNA as a template. Histones thereby play a central role in transcription regulation, DNA repair, DNA replication and chromosomal stability. DNA accessibility is regulated via a complex set of post-translational modifications of histones, also called histone code, and nucleosome remodeling. SUBUNIT: 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. SUBCELLULAR LOCATION: Nucleus. Chromosome. DEVELOPMENTAL STAGE: Expressed during S phase, then expression strongly decreases as cell division slows down during the process of differentiation. PTM: Acetylation is generally linked to gene activation. Acetylation on Lys-10 (H3K9ac) impairs methylation at Arg-9 (H3R8me2s). Acetylation on Lys-19 (H3K18ac) and Lys-24 (H3K24ac) favors methylation at Arg-18 (H3R17me). PTM: Citrullination at Arg-9 (H3R8ci) and/or Arg-18 (H3R17ci) by PADI4 impairs methylation and represses transcription. PTM: Asymmetric dimethylation at Arg-18 (H3R17me2a) by CARM1 is linked to gene activation. Symmetric dimethylation at Arg-9 (H3R8me2s) by PRMT5 is linked to gene repression. Asymmetric dimethylation at Arg-3 (H3R2me2a) by PRMT6 is linked to gene repression and is mutually exclusive with H3 Lys-5 methylation (H3K4me2 and H3K4me3). H3R2me2a is present at the 3' of genes regardless of their transcription state and is enriched on inactive promoters, while it is absent on active promoters. PTM: Methylation at Lys-5 (H3K4me), Lys-37 (H3K36me) and Lys-80 (H3K79me) are linked to gene activation. Methylation at Lys-5 (H3K4me) facilitates subsequent acetylation of H3 and H4. Methylation at Lys-80 (H3K79me) is associated with DNA double- strand break (DSB) responses and is a specific target for TP53BP1. Methylation at Lys-10 (H3K9me) and Lys-28 (H3K27me) are linked to gene repression. Methylation at Lys-10 (H3K9me) is a specific target for HP1 proteins (CBX1, CBX3 and CBX5) and prevents subsequent phosphorylation at Ser-11 (H3S10ph) and acetylation of H3 and H4. Methylation at Lys-5 (H3K4me) and Lys-80 (H3K79me) require preliminary monoubiquitination of H2B at 'Lys-120'. Methylation at Lys-10 (H3K9me) and Lys-28 (H3K27me) are enriched in inactive X chromosome chromatin. Monomethylation at Lys-57 (H3K56me1) by EHMT2/G9A in G1 phase promotes interaction with PCNA and is required for DNA replication. PTM: Phosphorylated at Thr-4 (H3T3ph) by GSG2/haspin during prophase and dephosphorylated during anaphase. Phosphorylation at Ser-11 (H3S10ph) by AURKB is crucial for chromosome condensation and cell-cycle progression during mitosis and meiosis. In addition phosphorylation at Ser-11 (H3S10ph) by RPS6KA4 and RPS6KA5 is important during interphase because it enables the transcription of genes following external stimulation, like mitogens, stress, growth factors or UV irradiation and result in the activation of genes, such as c-fos and c-jun. Phosphorylation at Ser-11 (H3S10ph), which is linked to gene activation, prevents methylation at Lys-10 (H3K9me) but facilitates acetylation of H3 and H4. Phosphorylation at Ser-11 (H3S10ph) by AURKB mediates the dissociation of HP1 proteins (CBX1, CBX3 and CBX5) from heterochromatin. Phosphorylation at Ser-11 (H3S10ph) is also an essential regulatory mechanism for neoplastic cell transformation. Phosphorylated at Ser-29 (H3S28ph) by MLTK isoform 1, RPS6KA5 or AURKB during mitosis or upon ultraviolet B irradiation. Phosphorylation at Thr-7 (H3T6ph) by PRKCB is a specific tag for epigenetic transcriptional activation that prevents demethylation of Lys-5 (H3K4me) by LSD1/KDM1A. At centromeres, specifically phosphorylated at Thr-12 (H3T11ph) from prophase to early anaphase, by DAPK3 and PKN1. Phosphorylation at Thr-12 (H3T11ph) by PKN1 is a specific tag for epigenetic transcriptional activation that promotes demethylation of Lys-10 (H3K9me) by KDM4C/JMJD2C. Phosphorylation at Thr-12 (H3T11ph) by chromatin- associated CHEK1 regulates the transcription of cell cycle regulatory genes by modulating acetylation of Lys-10 (H3K9ac). Phosphorylation at Tyr-42 (H3Y41ph) by JAK2 promotes exclusion of CBX5 (HP1 alpha) from chromatin. PTM: Monoubiquitinated by RAG1 in lymphoid cells, monoubiquitination is required for V(D)J recombination (By similarity). Ubiquitinated by the CUL4-DDB-RBX1 complex in response to ultraviolet irradiation. This may weaken the interaction between histones and DNA and facilitate DNA accessibility to repair proteins. PTM: Lysine deamination at Lys-5 (H3K4all) to form allysine is mediated by LOXL2. Allysine formation by LOXL2 only takes place on H3K4me3 and results in gene repression (PubMed:22483618). MISCELLANEOUS: This histone is only present in mammals and is enriched in acetylation of Lys-15 and dimethylation of Lys-10 (H3K9me2). SIMILARITY: Belongs to the histone H3 family. GENE SYNONYMS:HIST1H3A H3FA H3FL H3FC H3FB H3FD H3FI H3FH H3FK H3FF H3FJ. COPYRIGHT: Protein annotation is derived from the UniProt Consortium (http://www.uniprot.org/). Distributed under the Creative Commons Attribution-NoDerivs License., SEQUENCE 136 AA; 15404 MW; 9B89008EA50A0EF6 CRC64;
biopax3:xref
urn:biopax:RelationshipXref:HGNC_HGNC:4766, urn:biopax:RelationshipXref:HGNC_HGNC:4767, urn:biopax:RelationshipXref:HGNC_HGNC:4768, urn:biopax:RelationshipXref:HGNC_HGNC:4769, urn:biopax:RelationshipXref:HGNC_HGNC:4771, urn:biopax:RelationshipXref:HGNC_HGNC:4772, urn:biopax:RelationshipXref:HGNC_HGNC:4773, urn:biopax:RelationshipXref:HGNC_HGNC:4774, urn:biopax:RelationshipXref:HGNC_HGNC:4775, urn:biopax:RelationshipXref:HGNC_HGNC:4776, urn:biopax:RelationshipXref:NCBI GENE_8350, urn:biopax:RelationshipXref:NCBI GENE_8351, urn:biopax:RelationshipXref:NCBI GENE_8352, urn:biopax:RelationshipXref:NCBI GENE_8353, urn:biopax:RelationshipXref:NCBI GENE_8354, urn:biopax:RelationshipXref:NCBI GENE_8355, urn:biopax:RelationshipXref:NCBI GENE_8356, urn:biopax:RelationshipXref:NCBI GENE_8357, urn:biopax:RelationshipXref:NCBI GENE_8358, urn:biopax:RelationshipXref:NCBI GENE_8968, urn:biopax:RelationshipXref:REFSEQ_NP_003520, urn:biopax:RelationshipXref:REFSEQ_NP_003521, urn:biopax:RelationshipXref:REFSEQ_NP_003522, urn:biopax:RelationshipXref:REFSEQ_NP_003523, urn:biopax:RelationshipXref:REFSEQ_NP_003524, urn:biopax:RelationshipXref:REFSEQ_NP_003525, urn:biopax:RelationshipXref:REFSEQ_NP_003526, urn:biopax:RelationshipXref:REFSEQ_NP_003527, urn:biopax:RelationshipXref:REFSEQ_NP_003528, urn:biopax:RelationshipXref:REFSEQ_NP_066298, urn:biopax:UnificationXref:UNIPROT_A0PJT7, urn:biopax:UnificationXref:UNIPROT_A5PLR1, urn:biopax:UnificationXref:UNIPROT_P02295, urn:biopax:UnificationXref:UNIPROT_P02296, urn:biopax:UnificationXref:UNIPROT_P16106, urn:biopax:UnificationXref:UNIPROT_P68431, urn:biopax:UnificationXref:UNIPROT_Q6ISV8, urn:biopax:UnificationXref:UNIPROT_Q6NWP8, urn:biopax:UnificationXref:UNIPROT_Q6NWP9, urn:biopax:UnificationXref:UNIPROT_Q6NXU4, urn:biopax:UnificationXref:UNIPROT_Q71DJ3, urn:biopax:UnificationXref:UNIPROT_Q93081
biopax3:displayName
H31_HUMAN
biopax3:name
HIST1H3A, Histone H3/a, Histone H3/b, Histone H3/c, Histone H3/d, Histone H3/f, Histone H3/h, Histone H3/i, Histone H3/j, Histone H3/k, Histone H3/l
biopax3:entityFeature
urn:biopax:ModificationFeature:H31_HUMAN_37, urn:biopax:ModificationFeature:H31_HUMAN_3, urn:biopax:ModificationFeature:H31_HUMAN_40, urn:biopax:ModificationFeature:H31_HUMAN_36, urn:biopax:ModificationFeature:H31_HUMAN_20, urn:biopax:ModificationFeature:H31_HUMAN_22, urn:biopax:ModificationFeature:H31_HUMAN_28, urn:biopax:ModificationFeature:H31_HUMAN_6, urn:biopax:ModificationFeature:H31_HUMAN_44, urn:biopax:ModificationFeature:H31_HUMAN_26, urn:biopax:ModificationFeature:H31_HUMAN_8, urn:biopax:ModificationFeature:H31_HUMAN_29, urn:biopax:ModificationFeature:H31_HUMAN_15, urn:biopax:ModificationFeature:H31_HUMAN_12, urn:biopax:ModificationFeature:H31_HUMAN_9, urn:biopax:ModificationFeature:H31_HUMAN_24, urn:biopax:ModificationFeature:H31_HUMAN_34, urn:biopax:ModificationFeature:H31_HUMAN_14, urn:biopax:ModificationFeature:H31_HUMAN_11, urn:biopax:ModificationFeature:H31_HUMAN_10, urn:biopax:ModificationFeature:H31_HUMAN_21, urn:biopax:ModificationFeature:H31_HUMAN_2, urn:biopax:ModificationFeature:H31_HUMAN_19, urn:biopax:ModificationFeature:H31_HUMAN_38, urn:biopax:ModificationFeature:H31_HUMAN_45, urn:biopax:ModificationFeature:H31_HUMAN_7, urn:biopax:ModificationFeature:H31_HUMAN_31, urn:biopax:ModificationFeature:H31_HUMAN_33, urn:biopax:ModificationFeature:H31_HUMAN_32, urn:biopax:ModificationFeature:H31_HUMAN_1, urn:biopax:ModificationFeature:H31_HUMAN_39, urn:biopax:ModificationFeature:H31_HUMAN_18, urn:biopax:ModificationFeature:H31_HUMAN_42, urn:biopax:ModificationFeature:H31_HUMAN_13, urn:biopax:ModificationFeature:H31_HUMAN_5, urn:biopax:ModificationFeature:H31_HUMAN_35, urn:biopax:ModificationFeature:H31_HUMAN_30, urn:biopax:ModificationFeature:H31_HUMAN_25, urn:biopax:ModificationFeature:H31_HUMAN_17, urn:biopax:ModificationFeature:H31_HUMAN_16, urn:biopax:ModificationFeature:H31_HUMAN_4, urn:biopax:ModificationFeature:H31_HUMAN_43, urn:biopax:ModificationFeature:H31_HUMAN_41
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