Patatin-like phospholipase domain-containing protein 3 (PNPLA3), also known as adiponutrin (ADPN), acylglycerol O-acyltransferase or calcium-independent phospholipase A2-epsilon (iPLA2-epsilon) is an enzyme that in humans is encoded by the PNPLA3 gene.[5][6][7]

PNPLA3
Identifiers
AliasesPNPLA3, ADPN, C22orf20, iPLA(2)epsilon, patatin like phospholipase domain containing 3
External IDsOMIM: 609567; MGI: 2151796; HomoloGene: 11883; GeneCards: PNPLA3; OMA:PNPLA3 - orthologs
Orthologs
SpeciesHumanMouse
Entrez
Ensembl
UniProt
RefSeq (mRNA)

NM_025225

NM_054088

RefSeq (protein)

NP_079501

NP_473429
NP_001395268
NP_001395269
NP_001395270
NP_001395271

Location (UCSC)Chr 22: 43.92 – 43.96 MbChr 15: 84.05 – 84.07 Mb
PubMed search[3][4]
Wikidata
View/Edit HumanView/Edit Mouse

Function

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Adiponutrin is a triacylglycerol lipase that mediates triacylglycerol hydrolysis in adipocytes. The encoded protein, which appears to be membrane bound, may be involved in the balance of energy usage/storage in adipocytes.[7]

Genomics

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The gene is located on the long arm of chromosome 22 at band 13.31 (22q13.31). It lies on the Watson (plus) strand and is 40,750 bases in length.

Upstream of the gene, putative binding sites for several transcription factors have been identified. These include PPAR-gamma, POU2F1, and POU2F2. It is not known at present whether any of these transcriptions factors are actually involved in the regulation of this gene.

Biochemistry

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The recommended name for the gene product is patatin-like phospholipase domain-containing protein 3. It is a single-pass type II membrane protein and is a multifunctional enzyme with both triacylglycerol lipase and acylglycerol O-acyltransferase activities. It is involved in the triacylglycerol hydrolysis in adipocytes and may play a role in energy metabolism.

The mature protein is 481 amino acids in length and the predicted molecular weight is 52.865 kilodaltons (kDa). Two of the isoforms have been described, but the functional significance (if any) of these forms is not known.

Clinical relevance

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An association between alcoholic liver disease in caucasians and variations in this gene has been confirmed.[8] A mutation of isoleucine to methionine (I[ATC]>M[ATG]) SNP rs738409 has been confirmed to increase susceptibility to non-alcoholic liver disease and also to have effects in diabetes.[9]

References

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  1. ^ Jump up to: a b c GRCh38: Ensembl release 89: ENSG00000100344Ensembl, May 2017
  2. ^ Jump up to: a b c GRCm38: Ensembl release 89: ENSMUSG00000041653Ensembl, 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. ^ Wilson PA, Gardner SD, Lambie NM, Commans SA, Crowther DJ (September 2006). "Characterization of the human patatin-like phospholipase family". Journal of Lipid Research. 47 (9): 1940–9. doi:10.1194/jlr.M600185-JLR200. PMID 16799181.
  6. ^ Kienesberger PC, Oberer M, Lass A, Zechner R (April 2009). "Mammalian patatin domain containing proteins: a family with diverse lipolytic activities involved in multiple biological functions". Journal of Lipid Research. 50 Suppl (Suppl): S63-8. doi:10.1194/jlr.R800082-JLR200. PMC 2674697. PMID 19029121.
  7. ^ Jump up to: a b "Entrez Gene: PNPLA3 patatin-like phospholipase domain containing 3".
  8. ^ Stickel F, Hampe J (January 2012). "Genetic determinants of alcoholic liver disease". Gut. 61 (1): 150–9. doi:10.1136/gutjnl-2011-301239. PMID 22110053. S2CID 22559086.
  9. ^ Pingitore P, Romeo S (June 2019). "The role of PNPLA3 in health and disease". Biochimica et Biophysica Acta (BBA) - Molecular and Cell Biology of Lipids. 1864 (6): 900–906. doi:10.1016/j.bbalip.2018.06.018. PMID 29935383. S2CID 49392249.

Further reading

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