IDO2
Identifiers
AliasesIDO2, INDOL1, indoleamine 2,3-dioxygenase 2
External IDsOMIM: 612129 MGI: 2142489 HomoloGene: 48830 GeneCards: IDO2
Orthologs
SpeciesHumanMouse
Entrez

169355

209176

Ensembl

ENSG00000188676

ENSMUSG00000031549

UniProt

Q6ZQW0

Q8R0V5

RefSeq (mRNA)

NM_194294
NM_001395206

NM_145949

RefSeq (protein)

NP_919270

NP_666061

Location (UCSC)Chr 8: 39.93 – 40.02 MbChr 8: 25.02 – 25.07 Mb
PubMed search[3][4]
Wikidata
View/Edit HumanView/Edit Mouse

Indoleamine 2,3-dioxygenase 2 (IDO2) is a protein that in humans is encoded by the IDO2 gene.[5]

Function

IDO2 (indolamine-2,3-dioxygenase) is an enzyme with protein size of 420 amino acids (47 kDa) that is used for catabolism of tryptophan. In organisms, other enzymes participate in L-tryptophan cleavage, namely IDO1 and TDO. Despite of IDO1 and IDO2 are closely related enzymes originating by gene duplication and sharing high level (43%) of sequence homology,[6][7] they differentiate by their kinetics, function and expression pattern. Genes encoding IDO1 and IDO2 have similar genomic structure and are situated closely to each other on chromosome 8.[8] IDO2 is produced in a very limited type of tissues as kidney, liver or antigen presenting cells.[9] IDO2 is less active on substrates of IDO1, better catabolizing other Trp derivates as 5-methoxytryptophan. There are several isoforms in population that comes from alternative splicing.[10] As well as IDO1, IDO2 has been reported in Treg differentiation in vitro,[11] suggesting a role in tolerance maintenance. Its expression has been found in several cancers, gastric, colon or renal tumors.[12]

References

  1. 1 2 3 GRCh38: Ensembl release 89: ENSG00000188676 - Ensembl, May 2017
  2. 1 2 3 GRCm38: Ensembl release 89: ENSMUSG00000031549 - Ensembl, 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. "Entrez Gene: Indoleamine 2,3-dioxygenase 2".
  6. Yuasa HJ, Mizuno K, Ball HJ (July 2015). "Low efficiency IDO2 enzymes are conserved in lower vertebrates, whereas higher efficiency IDO1 enzymes are dispensable". The FEBS Journal. 282 (14): 2735–45. doi:10.1111/febs.13316. PMID 25950090. S2CID 25834690.
  7. Ball HJ, Sanchez-Perez A, Weiser S, Austin CJ, Astelbauer F, Miu J, McQuillan JA, Stocker R, Jermiin LS, Hunt NH (July 2007). "Characterization of an indoleamine 2,3-dioxygenase-like protein found in humans and mice". Gene. 396 (1): 203–13. doi:10.1016/j.gene.2007.04.010. PMID 17499941.
  8. Ball HJ, Sanchez-Perez A, Weiser S, Austin CJ, Astelbauer F, Miu J, McQuillan JA, Stocker R, Jermiin LS, Hunt NH (July 2007). "Characterization of an indoleamine 2,3-dioxygenase-like protein found in humans and mice". Gene. 396 (1): 203–13. doi:10.1016/j.gene.2007.04.010. PMID 17499941.
  9. Merlo LM, Mandik-Nayak L (2016). "IDO2: A Pathogenic Mediator of Inflammatory Autoimmunity". Clinical Medicine Insights. Pathology. 9 (Suppl 1): 21–28. doi:10.4137/CPath.S39930. PMC 5119657. PMID 27891058.
  10. Metz R, Duhadaway JB, Kamasani U, Laury-Kleintop L, Muller AJ, Prendergast GC (August 2007). "Novel tryptophan catabolic enzyme IDO2 is the preferred biochemical target of the antitumor indoleamine 2,3-dioxygenase inhibitory compound D-1-methyl-tryptophan". Cancer Research. 67 (15): 7082–7. doi:10.1158/0008-5472.CAN-07-1872. PMID 17671174.
  11. Metz R, Smith C, DuHadaway JB, Chandler P, Baban B, Merlo LM, Pigott E, Keough MP, Rust S, Mellor AL, Mandik-Nayak L, Muller AJ, Prendergast GC (July 2014). "IDO2 is critical for IDO1-mediated T-cell regulation and exerts a non-redundant function in inflammation". International Immunology. 26 (7): 357–67. doi:10.1093/intimm/dxt073. PMC 4432394. PMID 24402311.
  12. Löb S, Königsrainer A, Zieker D, Brücher BL, Rammensee HG, Opelz G, Terness P (January 2009). "IDO1 and IDO2 are expressed in human tumors: levo- but not dextro-1-methyl tryptophan inhibits tryptophan catabolism". Cancer Immunology, Immunotherapy. 58 (1): 153–7. doi:10.1007/s00262-008-0513-6. PMID 18418598. S2CID 6199515.

Further reading

This article incorporates text from the United States National Library of Medicine, which is in the public domain.


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