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RTP3 (gene)

From Wikipedia, the free encyclopedia

RTP3 (receptor transporter protein 3) is a gene located on chromosome 3 in humans that encodes the RTP3 protein.[1] Its expression is liver-restricted.[2]

Gene

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Aliases for RTP3 in Homo sapiens include LTM1, TMEM7, and Z3CXXC3.[1] It is located at locus 3p21.31 and contains two exons. It spans a total of 2,974 base pairs, between bases 46497976 and 46500950 on chromosome 3.[citation needed]

Protein

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There is only one known protein isoform in humans, which is 232 amino acids long and has a predicted molecular weight of 26.9 kDa.[3] It has a predicted isoelectric point of 9.[4] The protein contains a transmembrane domain near the C-terminus. The protein is rich in cysteine and tryptophan and is poor in aspartic acid.[5]

Gene regulation

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Regulation of the RTP3 gene appears to be tissue-specific, as it is expressed almost exclusively in the liver, with low levels of expression in the testes, thyroid, kidney, and adrenal gland.[1][6]

There are some poorly-conserved binding sites for miRNA molecules in the 3' untranslated region of the gene.[7] One of these is miRNA-29, which has been found to affect progression of liver tumors in mouse models.[8]

Homologs

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Orthologs

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Many animal species contain orthologs of the RTP3 gene, including various species of mammals, rodents, and birds.[9]

Paralogs

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RTP3 has several paralogs in humans, including other members of the RTP family.[9]

Interacting proteins

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While there is experimental evidence RTP3 may potentially be able to interact with proteins involved in olfactory signaling, as it contains shared homology with other members of the RTP family that do so, it is unlikely that it contributes greatly to olfactory signaling pathways due to its expression being almost exclusive to the liver.[10][11]

Clinical significance

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The RTP3 gene has been found to be downregulated in liver carcinomas.[12] In cell lines that do not contain p53, a tumor suppressor protein, RTP3 has found to be more highly expressed than in cell lines that do contain the protein.[13]

Single-nucleotide polymorphisms in the promoter and intron of the RTP3 gene have been associated with increased risk of hip fracture, suggesting possible involvement of the gene in the TGF-β signaling pathway.[11]

References

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  1. ^ a b c "RTP3 receptor transporter protein 3 [Homo sapiens (human)] - Gene - NCBI".
  2. ^ Fagerberg L, Hallström BM, Oksvold P, Kampf C, Djureinovic D, Odeberg J, Habuka M, Tahmasebpoor S, Danielsson A, Edlund K, Asplund A, Sjöstedt E, Lundberg E, Szigyarto CA, Skogs M, Takanen JO, Berling H, Tegel H, Mulder J, Nilsson P, Schwenk JM, Lindskog C, Danielsson F, Mardinoglu A, Sivertsson A, von Feilitzen K, Forsberg M, Zwahlen M, Olsson I, Navani S, Huss M, Nielsen J, Ponten F, Uhlén M (February 2014). "Analysis of the human tissue-specific expression by genome-wide integration of transcriptomics and antibody-based proteomics". Mol Cell Proteomics. 13 (2): 397–406. doi:10.1074/mcp.M113.035600. PMC 3916642. PMID 24309898.
  3. ^ "receptor-transporting protein 3 [Homo sapiens (human)] - Protein - NCBI".
  4. ^ "ExPASy - Compute pI/Mw tool".
  5. ^ Madeira F, Park YM, Lee J, Buso N, Gur T, Madhusoodanan N, Basutkar P, Tivey AR, Potter SC, Finn RD, Lopez R (July 2019). "The EMBL-EBI search and sequence analysis tools APIs in 2019". Nucleic Acids Res. 47 (W1): W636–W641. doi:10.1093/nar/gkz268. PMC 6602479. PMID 30976793.
  6. ^ She X, Rohl CA, Castle JC, Kulkarni AV, Johnson JM, Chen R (June 2009). "Definition, conservation and epigenetics of housekeeping and tissue-enriched genes". BMC Genomics. 10: 269. doi:10.1186/1471-2164-10-269. PMC 2706266. PMID 19534766.
  7. ^ Agarwal V, Bell GW, Nam JW, Bartel DP (August 2015). "Predicting effective microRNA target sites in mammalian mRNAs". eLife. 4. doi:10.7554/eLife.05005. PMC 4532895. PMID 26267216.
  8. ^ Tao J, Ji J, Li X, Ding N, Wu H, Liu Y, Wang XW, Calvisi DF, Song G, Chen X (March 2015). "Distinct anti-oncogenic effect of various microRNAs in different mouse models of liver cancer". Oncotarget. 6 (9): 6977–88. doi:10.18632/oncotarget.3166. PMC 4466663. PMID 25762642.
  9. ^ a b Yates AD, Achuthan P, Akanni W, Allen J, Allen J, Alvarez-Jarreta J, Amode MR, Armean IM, Azov AG, Bennett R, Bhai J, Billis K, Boddu S, Marugán JC, Cummins C, Davidson C, Dodiya K, Fatima R, Gall A, Giron CG, Gil L, Grego T, Haggerty L, Haskell E, Hourlier T, Izuogu OG, Janacek SH, Juettemann T, Kay M, Lavidas I, Le T, Lemos D, Martinez JG, Maurel T, McDowall M, McMahon A, Mohanan S, Moore B, Nuhn M, Oheh DN, Parker A, Parton A, Patricio M, Sakthivel MP, Abdul Salam AI, Schmitt BM, Schuilenburg H, Sheppard D, Sycheva M, Szuba M, Taylor K, Thormann A, Threadgold G, Vullo A, Walts B, Winterbottom A, Zadissa A, Chakiachvili M, Flint B, Frankish A, Hunt SE, IIsley G, Kostadima M, Langridge N, Loveland JE, Martin FJ, Morales J, Mudge JM, Muffato M, Perry E, Ruffier M, Trevanion SJ, Cunningham F, Howe KL, Zerbino DR, Flicek P (January 2020). "Ensembl 2020". Nucleic Acids Res. 48 (D1): D682–D688. doi:10.1093/nar/gkz966. PMC 7145704. PMID 31691826.
  10. ^ Behrens M, Bartelt J, Reichling C, Winnig M, Kuhn C, Meyerhof W (July 2006). "Members of RTP and REEP gene families influence functional bitter taste receptor expression". J Biol Chem. 281 (29): 20650–9. doi:10.1074/jbc.M513637200. PMID 16720576. S2CID 45020418.
  11. ^ a b Zhao LJ, Liu XG, Liu YZ, Liu YJ, Papasian CJ, Sha BY, Pan F, Guo YF, Wang L, Yan H, Xiong DH, Tang ZH, Yang TL, Chen XD, Guo Y, Li J, Shen H, Zhang F, Lei SF, Recker RR, Deng HW (February 2010). "Genome-wide association study for femoral neck bone geometry". J Bone Miner Res. 25 (2): 320–9. doi:10.1359/jbmr.090726. PMC 3153387. PMID 20175129.
  12. ^ Zhou X, Popescu NC, Klein G, Imreh S (August 2007). "The interferon-alpha responsive gene TMEM7 suppresses cell proliferation and is downregulated in human hepatocellular carcinoma". Cancer Genet Cytogenet. 177 (1): 6–15. doi:10.1016/j.cancergencyto.2007.04.007. PMC 2034301. PMID 17693185.
  13. ^ Lee YH, Andersen JB, Song HT, Judge AD, Seo D, Ishikawa T, Marquardt JU, Kitade M, Durkin ME, Raggi C, Woo HG, Conner EA, Avital I, Maclachlan I, Factor VM, Thorgeirsson SS (November 2010). "Definition of ubiquitination modulator COP1 as a novel therapeutic target in human hepatocellular carcinoma". Cancer Res. 70 (21): 8264–9. doi:10.1158/0008-5472.CAN-10-0749. PMC 2970744. PMID 20959491.
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