Nucleoporin 62

NUP62
Available structures PDB Ortholog search: PDBe RCSB List of PDB id codes 5IJN, 5IJO
Identifiers
Aliases	NUP62, IBSN, SNDI, p62, nucleoporin 62kDa, nucleoporin 62
External IDs	OMIM: 605815 MGI: 1351500 HomoloGene: 68773 GeneCards: NUP62
Gene location (Human) Chr. Chromosome 19 (human)[1] Band No data available Start 49,906,825 bp[1] End 49,929,763 bp[1]
Gene location (Mouse) Chr. Chromosome 7 (mouse)[2] Band No data available Start 44,816,088 bp[2] End 44,830,812 bp[2]
Gene ontology Molecular function • Hsp90 protein binding • SH2 domain binding • chromatin binding • thyroid hormone receptor binding • PTB domain binding • Hsp70 protein binding • protein binding • ubiquitin binding • kinesin binding • receptor signaling complex scaffold activity • structural constituent of nuclear pore • phospholipid binding • nucleocytoplasmic transporter activity Cellular component • nuclear membrane • intracellular membrane-bounded organelle • Flemming body • nuclear pore • intracellular ribonucleoprotein complex • protein complex • annulate lamellae • cytoskeleton • nucleus • nuclear pore central transport channel • spindle pole • cytoplasm • centrosome • mitotic spindle • nuclear envelope • microtubule organizing center • host cell Biological process • mRNA transport • negative regulation of epidermal growth factor receptor signaling pathway • viral transcription • regulation of Ras protein signal transduction • cell death • negative regulation of apoptotic process • protein sumoylation • transcription, DNA-templated • negative regulation of Ras protein signal transduction • positive regulation of transcription, DNA-templated • cell aging • cell surface receptor signaling pathway • mitotic nuclear envelope disassembly • regulation of signal transduction • negative regulation of MAP kinase activity • spermatogenesis • regulation of protein import into nucleus • hormone-mediated signaling pathway • regulation of cellular response to heat • positive regulation of I-kappaB kinase/NF-kappaB signaling • protein transport • negative regulation of programmed cell death • nuclear transport • protein heterotrimerization • viral process • positive regulation of epidermal growth factor receptor signaling pathway • negative regulation of cell proliferation • intracellular transport of virus • ribonucleoprotein complex export from nucleus • protein import into nucleus • tRNA export from nucleus • mRNA export from nucleus • mitotic metaphase plate congression • mitotic centrosome separation • positive regulation of mitotic nuclear division • positive regulation of centriole replication • regulation of mitotic spindle organization • centriole assembly • positive regulation of mitotic cytokinetic process • positive regulation of protein localization to centrosome • centrosome cycle • mitotic cell cycle • regulation of gene silencing by miRNA • regulation of glycolytic process • transport Sources:Amigo / QuickGO
Orthologs
Species	Human	Mouse
Entrez	23636	18226
Ensembl	ENSG00000213024	ENSMUSG00000109511
UniProt	P37198	Q63850
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 Mb	Chr 19: 44.82 – 44.83 Mb
PubMed search	[3]	[4]
Wikidata
View/Edit Human View/Edit Mouse

Nucleoporin p62 (p62) is a protein complex associated with the nuclear envelope. The p62 protein remains associated with the nuclear pore complex-lamina fraction. p62 is synthesized as a soluble cytoplasmic precursor of 61 kDa^[5] followed by modification that involve addition of N-acetylglucosamine residues,^[6] followed by association with other complex proteins.

The nuclear pore complex is a massive structure that extends across the nuclear envelope, forming a gateway that regulates the flow of macromolecules between the nucleus and the cytoplasm. Nucleoporins are the main components of the nuclear pore complex in eukaryotic cells. The protein encoded by this gene is a member of 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. Glycosylation 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.^[15] Karyopherin beta2 (transportin), a riboprotein transporter also interacts with p62.^[16] P62 also interacts with 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

Antibodies to p62 complex are involved in one or more autoimmune diseases. P62 glycosylation is increased in diabetes^[19] and may influence its association with other diseases. p62 is also more frequent in Stage IV primary biliary cirrhosis and is prognostic for severe disease.^[20]

Interactions

Nucleoporin 62 has been shown to interact with:

• HSF2,^[21]
• KPNB1,^[15][22]
• NUTF2,^[23][24]
• TRAF3,^[25] and
• XPO1,^[26][27]
• Nup93.^[17]

References

Further reading