Death-associated protein 6

DAXX
Available structures PDB Ortholog search: PDBe RCSB List of PDB id codes 4HGA, 2KQS, 2KZS, 2KZU, 4H9N, 4H9O, 4H9P, 4H9Q, 4H9R, 4H9S
Identifiers
Aliases	DAXX, BING2, DAP6, EAP1, death-domain associated protein, death domain associated protein, SMIM40
External IDs	OMIM: 603186; MGI: 1197015; HomoloGene: 1033; GeneCards: DAXX; OMA:DAXX - orthologs
Gene location (Human) Chr. Chromosome 6 (human)[1] Band 6p21.32 Start 33,318,558 bp[1] End 33,323,016 bp[1]
Gene location (Mouse) Chr. Chromosome 17 (mouse)[2] Band 17 B1|17 17.98 cM Start 34,128,388 bp[2] End 34,134,564 bp[2]
RNA expression pattern Bgee Human Mouse (ortholog) Top expressed in granulocyte lymph node appendix spleen ventricular zone stromal cell of endometrium blood left testis left adrenal gland left uterine tube Top expressed in spermatocyte spermatid genital tubercle seminiferous tubule granulocyte zygote tail of embryo internal carotid artery secondary oocyte thymus More reference expression data BioGPS More reference expression data
Gene ontology Molecular function heat shock protein binding protein homodimerization activity protein N-terminus binding histone binding p53 binding protein kinase activator activity protein binding enzyme binding ubiquitin protein ligase binding transcription factor binding androgen receptor binding protein kinase binding transcription coactivator activity transcription corepressor activity SUMO binding protein heterodimerization activity Cellular component cytosol PML body SWI/SNF superfamily-type complex chromosome nucleolus chromosome, centromeric region nucleoplasm nucleus cytoplasm nuclear body Biological process androgen receptor signaling pathway chromatin remodeling nucleosome assembly positive regulation of protein phosphorylation regulation of transcription, DNA-templated regulation of protein ubiquitination positive regulation of neuron death transcription, DNA-templated viral process negative regulation of transcription, DNA-templated extrinsic apoptotic signaling pathway via death domain receptors positive regulation of protein kinase activity apoptotic process cellular response to heat Unfolded Protein Response cellular response to cadmium ion cellular response to copper ion cellular response to diamide cellular response to sodium arsenite chromatin organization positive regulation of nucleic acid-templated transcription regulation of apoptotic process Sources:Amigo / QuickGO
Orthologs Species Human Mouse Entrez 1616 13163 Ensembl ENSG00000231617 ENSG00000206206 ENSG00000227046 ENSG00000206279 ENSG00000204209 ENSG00000229396 ENSMUSG00000002307 UniProt Q9UER7 Q4VX54 O35613 RefSeq (mRNA) NM_001141969 NM_001141970 NM_001254717 NM_001350 NM_001199733 NM_007829 NM_001355704 RefSeq (protein) NP_001135441 NP_001135442 NP_001241646 NP_001341 NP_001186662 NP_031855 NP_001342633 Location (UCSC) Chr 6: 33.32 – 33.32 Mb Chr 17: 34.13 – 34.13 Mb PubMed search [3] [4]
Wikidata
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Death-associated protein 6 also known as Daxx is a protein that in humans is encoded by the DAXX gene.^[5][6]

Daxx, a Death domain-associated protein, was first discovered through its cytoplasmic interaction with the classical death receptor Fas. It has been associated with heterochromatin and PML-NBs (Promyelocytic Leukaemia nuclear bodies) and has been implicated in many nuclear processes including transcription and cell cycle regulation.

This gene encodes a multifunctional protein that resides in multiple locations in the nucleus and the cytoplasm. Daxx serves as an H3.3 specific histone chaperone, interacting with an H3.3/H4 dimer.^[7] It interacts with a wide variety of proteins, such as apoptosis antigen Fas, centromere protein C, and transcription factor erythroblastosis virus E26 oncogene homolog 1 (ETS1). In the nucleus, the encoded protein functions as a potent transcription repressor that binds to sumoylated transcription factors. Its repression can be relieved by the sequestration of this protein into promyelocytic leukemia nuclear bodies or nucleoli. This protein also associates with centromeres in the G2 phase. In the cytoplasm, the encoded protein may function to regulate apoptosis. The subcellular localization and function of this protein are modulated by post-translational modifications, including sumoylation, phosphorylation and polyubiquitination.^[8]

Daxx is uniformly expressed throughout the body, except in the testes and thymus, which have especially high expression of the protein. At the level of the cell, Daxx is found in the cytoplasm, interacting with Fas-receptor or other cytoplasmic molecules, as well as in the nucleus, where it interacts with some subnuclear structures. Several additional interacting proteins are known, but not always is there an understanding of the specific function and relevance of this interaction.

When the PML-NB is absent or disrupted, Daxx is delocalized and apoptosis does not occur. This interaction was demonstrated when PML-NB disrupted cells were treated and Daxx relocalized with the PML-NB. ATRX, a centromeric heterochromatin component co-localizes with Daxx. This partnership is found mainly in the S-phase of the cell cycle. No expression of Daxx leads to malfunction of S phase and cells with two nuclei are formed. Another centromeric component, CENP-C, associates with Daxx during interphase. While at first Daxx was said to be a "death protein", it is suggested that associating with centromeric components leads to another function of Daxx.

Fas-receptor stimulation causes Daxx to translocate out of the nucleus and into the cytoplasm. The breakdown of glucose produces reactive oxygen species (ROS). These induce extracellular Daxx to translocalize into the cytoplasm following an association with ASK1 (Apoptosis signal-regulating kinase1). Another mechanism for exogenous Daxx import involves CRM1. This transport mechanism is phosphorylation dependent. Nevertheless, it is not known whether the Fas-receptor stimuli or the ASK1 overexpression are caused by ROS or CRM1 mediated export.

After Fas stimulation, Daxx is activated and plays its role of pro-apoptotic protein in activating the c-JUN-N-Terminal Kinase (JNK) pathway. This pathway normally regulates stress-induced cell death. It is also essential for development of nerval system by programmed cell death. The real apoptotic process starts after activating this pathway. Daxx does not activate JNK itself but rather the upstream JNK kinase kinase ASK1. Some kind of positive feedback system was also discovered; JNK activates HIPK2, which stands for the translocation of nuclear Daxx to the cytoplasm. In turn, Daxx activates ASK1.

TGF-β regulates a variety of different cellular developmental processes including growth, differentiation, proliferation, and cell death. Daxx interacts with the TGF-β type II receptor by binding of C-terminal domain of the protein. When the cell is treated with TGF-β, HIPK2, a nuclear kinase, phosphorylates Daxx and the activated Daxx in turn activates the JNK pathway (see "The Daxx Pathway" figure).

Glucose breakdown produces ROS, which leads to Daxx production and relocalization, activating JNK pathway in turn. Another inducer of Daxx production is the exposure to UV-radiation. ASK1 will be transported to the nucleus when UV-irradiation is used to treat the cell. It is still unknown as to whether ASK1 binds Daxx, due to UV-irradiation. Another important cell death-property of Daxx is the association with PML-NB. It was shown that Daxx associates with Pml only when exposed to high oxidative stress or UV-irradiation. Another study showed loss of Daxx pro-apoptotic function in case of a mutant without Pml.

A rather surprising property of Daxx is its anti-apoptotic function. When Daxx was not expressed or disrupted during embryonic development, it resulted in an early stage lethality. Other studies showed that lack of Daxx gene caused a higher apoptotic rate in embryonic stem cells. Only when Daxx was bound to Pml were apoptosis rates higher, suggesting that associated cytoplasmic Daxx has the role of an anti-apoptotic molecule.

The omnipresence of Daxx in the cell nucleus suggests that the protein may also function as a transcription factor. Although it contains no known DNA-binding domains, Daxx can interact and suppress several transcription factors, such as p53, p73, and NF-κB. Proteins other than transcription factors are also blocked or inhibited by Daxx, such as the TGF-β pathway regulator, Smad4, conferring upon Daxx a major role in TGF-β signaling.

• DAXX+protein,+human at the U.S. National Library of Medicine Medical Subject Headings (MeSH)
• PDBe-KB provides an overview of all the structure information available in the PDB for Human Death domain-associated protein 6

This article incorporates text from the United States National Library of Medicine, which is in the public domain.