Far upstream element–binding protein 1

Protein-coding gene in the species Homo sapiens From Wikipedia, the free encyclopedia

Far upstream element-binding protein 1 is a protein that in humans is encoded by the FUBP1 gene.[5][6]

PDBOrtholog search: PDBe RCSB
AliasesFUBP1, FBP, FUBP, hDH V, far upstream element binding protein 1
Quick facts FUBP1, Available structures ...
FUBP1
Available structures
PDBOrtholog search: PDBe RCSB
Identifiers
AliasesFUBP1, FBP, FUBP, hDH V, far upstream element binding protein 1
External IDsOMIM: 603444; MGI: 1196294; HomoloGene: 48253; GeneCards: FUBP1; OMA:FUBP1 - orthologs
Orthologs
SpeciesHumanMouse
Entrez
Ensembl
UniProt
RefSeq (mRNA)

NM_001303433
NM_003902
NM_001376055
NM_001376056
NM_001376057

RefSeq (protein)

NP_001290362
NP_003893
NP_001362984
NP_001362985
NP_001362986

Location (UCSC)Chr 1: 77.94 – 77.98 MbChr 3: 151.92 – 151.94 Mb
PubMed search[3][4]
Wikidata
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This gene encodes a ssDNA binding protein that activates the far upstream element (FUSE) of c-myc and stimulates expression of c-myc in undifferentiated cells. Regulation of FUSE by FUBP occurs through single-strand binding of FUBP to the non-coding strand. This protein has been shown to function as an ATP-dependent DNA helicase.[6]

Interactions

Far upstream element-binding protein 1 has been shown to interact with MAPK14[7] and SMN1.[8]

Clinical Significance

FUBP1 gene deletion forms part of the 1p/19q codeletion mutation seen in oligodendroglioma, a form of primary brain tumour.[9] CIC gene is also lost in the 1p/19q codeletion mutation.

References

Further reading

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