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PABPN1

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

Polyadenylate-binding protein 2 (PABP-2) also known as polyadenylate-binding nuclear protein 1 (PABPN1) is a protein that in humans is encoded by the PABPN1 gene.[5][6] PABPN1 is a member of a larger family of poly(A)-binding proteins in the human genome.

AliasesPABPN1, OPMD, PAB2, PABII, PABP-2, PABP2, poly(A) binding protein nuclear 1
PDBOrtholog search: PDBe RCSB
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PABPN1
Identifiers
AliasesPABPN1, OPMD, PAB2, PABII, PABP-2, PABP2, poly(A) binding protein nuclear 1
External IDsOMIM: 602279; MGI: 1859158; GeneCards: PABPN1
Available structures
PDBOrtholog search: PDBe RCSB
Orthologs
DatabasesNCBI: entry; OMA: entry
SpeciesHumanMouse
Entrez
Ensembl
UniProt
RefSeq (mRNA)

NM_004643
NM_001360551
NM_001360552

NM_019402

RefSeq (protein)

NP_004634
NP_001347480
NP_001347481

NP_062275

Location (UCSC)Chr 14: 23.32 – 23.33 MbChr 14: 55.13 – 55.14 Mb
PubMed search[3][4]
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Function

This gene encodes an abundant nuclear protein that binds with high affinity to nascent poly(A) tails. The protein is required for progressive and efficient polymerization of poly(A) tails on the 3' ends of eukaryotic genes and controls the size of the poly(A) tail to about 250 nt. At steady-state, this protein is localized in the nucleus whereas a different poly(A) binding protein is localized in the cytoplasm. An expansion of the trinucleotide (GCN) repeat from normal 10 to 11–17 at the 5' end of the coding region of this gene leads to autosomal dominant oculopharyngeal muscular dystrophy (OPMD) disease.[7] Multiple splice variants have been described but their full-length nature is not known. One splice variant includes introns 1 and 6 but no protein is formed.[6]

Interactions

PABPN1 has been shown to interact with SNW1.[8]

References

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