Ewing sarcoma breakpoint region 1

Last updated
EWSR1
Protein EWSR1 PDB 2cpe.png
Available structures
PDB Human UniProt search: PDBe RCSB
Identifiers
Aliases EWSR1 , EWS, bK984G1.4, EWS-FLI1, Ewing sarcoma breakpoint region 1, EWS RNA binding protein 1
External IDs OMIM: 133450 HomoloGene: 136069 GeneCards: EWSR1
Gene location (Human)
Ideogram human chromosome 22.svg
Chr. Chromosome 22 (human) [1]
Human chromosome 22 ideogram.svg
HSR 1996 II 3.5e.svg
Red rectangle 2x18.png
Band 22q12.2Start29,268,009 bp [1]
End29,300,525 bp [1]
RNA expression pattern
PBB GE EWSR1 210012 s at fs.png
More reference expression data
Orthologs
SpeciesHumanMouse
Entrez
Ensembl
UniProt
RefSeq (mRNA)

NM_001163285
NM_001163286
NM_001163287
NM_005243
NM_013986

Contents

n/a

RefSeq (protein)

NP_001156757
NP_001156758
NP_001156759
NP_005234
NP_053733

n/a

Location (UCSC) Chr 22: 29.27 – 29.3 Mb n/a
PubMed search [2] n/a
Wikidata
View/Edit Human

RNA-binding protein EWS is a protein that in humans is encoded by the EWSR1 gene on human chromosome 22, specifically 22q12.2. [3] [4] This region of chromosome 22 encodes the N-terminal transactivation domain of the EWS protein and that region may become joined to one of several other chromosomes which encode various transcription factors, see [5] The expression of a chimeric protein with the EWS transactivation domain fused to the DNA binding region of a transcription factor generates a powerful oncogenic protein causing Ewing sarcoma and other members of the Ewing family of tumors. These translocations can occur due to chromoplexy, a burst of complex chromosomal rearrangements seen in cancer cells. [6] The normal EWS gene encodes a RNA binding protein closely related to FUS (gene) and TAF15, all of which have been associated to amyotrophic lateral sclerosis. [7]

Interactions

The EWS protein has been shown to interact with:

Related Research Articles

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Fusion gene the result of gene fusion

A fusion gene is a hybrid gene formed from two previously independent genes. It can occur as a result of translocation, interstitial deletion, or chromosomal inversion. Fusion genes have been found to be prevalent in all main types of human neoplasia. The identification of these fusion genes play a prominent role in being a diagnostic and prognostic marker.

PAX3 protein-coding gene in the species Homo sapiens

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Ewings sarcoma bone cancer that has material basis in neural crest cells derives from undeveloped, undifferentiated neuroectoderm

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Neuron-derived orphan receptor 1 protein-coding gene in the species Homo sapiens

The neuron-derived orphan receptor 1 (NOR1) also known as NR4A3 is a protein that in humans is encoded by the NR4A3 gene. NOR1 is a member of the nuclear receptor family of intracellular transcription factors.

NFATC2 protein-coding gene in the species Homo sapiens

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FLI1 protein-coding gene in the species Homo sapiens

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ATF1 protein-coding gene in the species Homo sapiens

Cyclic AMP-dependent transcription factor ATF-1 is a protein that in humans is encoded by the ATF1 gene.

ETV4 protein-coding gene in the species Homo sapiens

ETS translocation variant 4 (ETV4), also known as polyoma enhancer activator 3 (PEA3), is a member of the PEA3 subfamily of Ets transcription factors.

DEK (gene) protein-coding gene in the species Homo sapiens

The human DEKgene encodes the DEK protein.

<i>ERG</i> (gene) protein-coding gene in the species Homo sapiens

ERG is an oncogene. ERG is a member of the ETS family of transcription factors. The ERG gene encodes for a protein, also called ERG, that functions as a transcriptional regulator. Genes in the ETS family regulate embryonic development, cell proliferation, differentiation, angiogenesis, inflammation, and apoptosis.

FUS (gene) protein-coding gene in the species Homo sapiens

RNA-binding protein FUS/TLS is a protein that in humans is encoded by the FUS gene.

SSX2 mammalian protein found in Homo sapiens

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SS18 protein-coding gene in the species Homo sapiens

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TAF15 protein-coding gene in the species Homo sapiens

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ETS transcription factor family protein family

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Myxoid liposarcoma Human disease

A myxoid liposarcoma is a malignant adipose tissue neoplasm of myxoid appearance histologically.

Extraskeletal myxoid chondrosarcoma (EMC) is a rare low-grade malignant mesenchymal neoplasm of the soft tissues, that differs from other sarcomas by unique histology and characteristic chromosomal translocation. There is an uncertain differentiation and neuroendocrine differentiation is even possible.

CREB3L1 protein-coding gene in the species Homo sapiens

CAMP responsive element binding protein 3 like 1 is a responsive element binding protein that in humans is encoded by the CREB3L1 gene.

EWS/FLI1 is an oncogenic protein that is pathognomonic for Ewing sarcoma. It is found in approximately 90% of all Ewing sarcoma tumors with the remaining 10% of fusions substituting one fusion partner with a closely related family member.

References

  1. 1 2 3 GRCh38: Ensembl release 89: ENSG00000182944 - Ensembl, May 2017
  2. "Human PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
  3. Delattre O, Zucman J, Plougastel B, Desmaze C, Melot T, Peter M, Kovar H, Joubert I, de Jong P, Rouleau G (October 1992). "Gene fusion with an ETS DNA-binding domain caused by chromosome translocation in human tumours". Nature. 359 (6391): 162–5. Bibcode:1992Natur.359..162D. doi:10.1038/359162a0. PMID   1522903.
  4. "Entrez Gene: EWSR1 Ewing sarcoma breakpoint region 1".
  5. "EWS family fusion genes - OMIM".
  6. Anderson ND, de Borja R, Young MD, Fuligni F, Rosic A, Roberts ND, Hajjar S, Layeghifard M, Novokmet A, Kowalski PE, Anaka M (August 2018). "Rearrangement bursts generate canonical gene fusions in bone and soft tissue tumors". Science. 361 (6405): eaam8419. doi:10.1126/science.aam8419. PMC   6176908 . PMID   30166462.
  7. Couthouis J, Hart MP, Erion R, King OD, Diaz Z, Nakaya T, Ibrahim F, Kim HJ, Mojsilovic-Petrovic J, Panossian S, Kim CE, Frackelton EC, Solski JA, Williams KL, Clay-Falcone D, Elman L, McCluskey L, Greene R, Hakonarson H, Kalb RG, Lee VM, Trojanowski JQ, Nicholson GA, Blair IP, Bonini NM, Van Deerlin VM, Mourelatos Z, Shorter J, Gitler AD (2012). "Evaluating the role of the FUS/TLS-related gene EWSR1 in amyotrophic lateral sclerosis". Hum. Mol. Genet. 21 (13): 2899–911. doi:10.1093/hmg/dds116. PMC   3373238 . PMID   22454397.
  8. Fujimura Y, Ohno T, Siddique H, Lee L, Rao VN, Reddy ES (January 1996). "The EWS-ATF-1 gene involved in malignant melanoma of soft parts with t(12;22) chromosome translocation, encodes a constitutive transcriptional activator". Oncogene. 12 (1): 159–67. PMID   8552387.
  9. Spahn L, Petermann R, Siligan C, Schmid JA, Aryee DN, Kovar H (August 2002). "Interaction of the EWS NH2 terminus with BARD1 links the Ewing's sarcoma gene to a common tumor suppressor pathway". Cancer Res. 62 (16): 4583–7. PMID   12183411.
  10. Ohno T, Ouchida M, Lee L, Gatalica Z, Rao VN, Reddy ES (Oct 1994). "The EWS gene, involved in Ewing family of tumors, malignant melanoma of soft parts and desmoplastic small round cell tumors, codes for an RNA binding protein with novel regulatory domains". Oncogene. 9 (10): 3087–97. PMID   8084618.
  11. Thomas GR, Latchman DS (2002). "The pro-oncoprotein EWS (Ewing's Sarcoma protein) interacts with the Brn-3a POU transcription factor and inhibits its ability to activate transcription". Cancer Biol. Ther. 1 (4): 428–32. doi: 10.4161/cbt.1.4.23 . PMID   12432261.
  12. Felsch JS, Lane WS, Peralta EG (May 1999). "Tyrosine kinase Pyk2 mediates G-protein-coupled receptor regulation of the Ewing sarcoma RNA-binding protein EWS". Curr. Biol. 9 (9): 485–8. doi:10.1016/s0960-9822(99)80214-0. PMID   10322114.
  13. Zhang D, Paley AJ, Childs G (July 1998). "The transcriptional repressor ZFM1 interacts with and modulates the ability of EWS to activate transcription". J. Biol. Chem. 273 (29): 18086–91. doi: 10.1074/jbc.273.29.18086 . PMID   9660765.
  14. Knoop LL, Baker SJ (August 2000). "The splicing factor U1C represses EWS/FLI-mediated transactivation". J. Biol. Chem. 275 (32): 24865–71. doi: 10.1074/jbc.M001661200 . PMID   10827180.
  15. Rual JF, Venkatesan K, Hao T, Hirozane-Kishikawa T, Dricot A, Li N, Berriz GF, Gibbons FD, Dreze M, Ayivi-Guedehoussou N, Klitgord N, Simon C, Boxem M, Milstein S, Rosenberg J, Goldberg DS, Zhang LV, Wong SL, Franklin G, Li S, Albala JS, Lim J, Fraughton C, Llamosas E, Cevik S, Bex C, Lamesch P, Sikorski RS, Vandenhaute J, Zoghbi HY, Smolyar A, Bosak S, Sequerra R, Doucette-Stamm L, Cusick ME, Hill DE, Roth FP, Vidal M (October 2005). "Towards a proteome-scale map of the human protein-protein interaction network". Nature. 437 (7062): 1173–8. Bibcode:2005Natur.437.1173R. doi:10.1038/nature04209. PMID   16189514.

Further reading