Nuclear pore glycoprotein p62

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(Redirected from
Nucleoporin 62
)
NUP62
Gene ontology
Molecular function
Cellular component
Biological process
Sources:Amigo / QuickGO
Ensembl
UniProt
RefSeq (mRNA)

NM_153719
NM_001193357
NM_012346
NM_016553
NM_153718

NM_053074

RefSeq (protein)

NP_001180286
NP_036478
NP_057637
NP_714940
NP_714941

NP_444304

Location (UCSC)Chr 19: 49.91 – 49.93 MbChr 7: 44.47 – 44.48 Mb
PubMed search[3][4]
Wikidata
View/Edit HumanView/Edit Mouse

Nuclear pore glycoprotein p62 is a protein complex associated with the

cytoplasmic precursor of 61 kDa[5] followed by modification that involve addition of N-acetylglucosamine residues,[6]
followed by association with other complex proteins. In humans it is encoded by the NUP62 gene.

The

FG repeat containing nucleoporins and is localized to the nuclear pore central plug. This protein associates with the importin alpha/beta complex which is involved in the import of proteins containing nuclear localization signals. Multiple transcript variants of this gene encode a single protein isoform.[7]

Structure

P62 is a serine/threonine rich protein of ~520 amino acids, with tetrapeptide repeats on the amino terminus and a series of alpha-helical regions with hydrophobic heptad repeats[8] forming beta-propeller domain. P62 assembles into a complex containing 3 addition proteins, p60, p54 and p45 [9][10] forming the p62 complex of ~235 kDa. O-GlcNAcylation appears to be involved in the assembly and disassembly of p62 into higher order complexes, and a serine/threonine rich linker region between Ser270 to Thr294 appear to be regulatory.[11] The p62 complex is localized to both the nucleoplasmic and cytoplasmic sides of the pore complex and the relative diameter of p62 complex relative to the nuclear pore complex suggests it interacts in pore gating.[12]

Function

P62 appears to interact with mRNA during transport out of the nucleus.[13] P62 also interacts with a nuclear transport factor (NTF2) protein that is involved in trafficking proteins between cytoplasm and nucleus.[14] Another protein, importin (beta) binds to the helical rod section of p62, which also binds NTF2 suggesting the formation of a higher order gating complex.

Nup93,[17] and when Nup98 is depleted p62 fails to assemble with nuclear pore complexes.[18]
Mutant pores could not dock/transport proteins with nuclear localization signals or M9 import signals.

Pathology

primary biliary cirrhosis and is prognostic for severe disease.[20]

Interactions

Nucleoporin 62 has been shown to

interact
with:

References

  1. ^ a b c GRCh38: Ensembl release 89: ENSG00000213024Ensembl, May 2017
  2. ^ a b c GRCm38: Ensembl release 89: ENSMUSG00000109511Ensembl, May 2017
  3. ^ "Human PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
  4. ^ "Mouse PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
  5. S2CID 22170880
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  7. ^ "Entrez Gene: NUP62 nucleoporin 62kDa".
  8. PMID 2190987
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Further reading