Transmembrane protein 222 is a protein that in humans is encoded by the TMEM222gene.[5][6] One notable feature of the protein encoded by this gene is the presence of three predicted transmembrane domains.[7] The TMEM222 protein is predicted to most likely localize to the secretory vesicles.[8]
TMEM222 has a domain of unknown function (DUF778).[9] Aliases of this gene include DKFZP564D0478, RP11-4K3__A.4, C1orf160, and MGC111002.[10] Accession NM_032125.2, the longest coding sequence (1629 bp), encodes a protein of 208 amino acid residues (23230 daltons), which is considered the consensus coding sequence (CCDS297.2).[11] There are two isoforms of the protein encoded by this gene. They are similar except the second (Q9H0R3-2) is lacking the first 96 amino acid residues that are present in the first (Q9H0R3-1).[12]
Gene Expression
ACEVIEW has labeled TMEM222 as highly expressed with 3.8 times more expression than the average gene in the database.[13] There is expression evidence from 166 tissues including brain, lung, colon, kidney, and placenta.[13]
Homology
Orthologs and distant homologs of the human TMEM222 have been identified throughout Eukaryota especially in plants and animals.[14] No paralogs of this gene have been found in the human genome.[15]
A distant homolog of TMEM222,[14] RTH (RTE1-Homolog),[16] is a homolog of RTE1 (Reversion-to-Ethylene Perception 1), which is known to induce conformational changes in ETR1 (Ethylene receptor 1) that result in negative regulation corresponding with loss of ethylene perception.[17]
Protein Interactions
Evidence from yeast two-hybrid screening exists for two protein interactions with this gene. One is a serine protease (PRSS23)[18] that has been identified to be involved in mouse ovulation and is excreted into the extracellular matrix.[19] The other protein is an ab-hydrolase (HLA-B associated transcript 5)[20] that is integral to the membrane, and its corresponding gene is located in the genome near Tumor Necrosis Factor (TNF)-alpha and TNF-beta.[21]
↑ Stelzl U, Worm U, Lalowski M, Haenig C, Brembeck FH, Goehler H, Stroedicke M, Zenkner M, Schoenherr A, Koeppen S, Timm J, Mintzlaff S, Abraham C, Bock N, Kietzmann S, Goedde A, Toksöz E, Droege A, Krobitsch S, Korn B, Birchmeier W, Lehrach H, Wanker EE (September 2005). "A human protein-protein interaction network: a resource for annotating the proteome". Cell. 122 (6): 957–68. doi:10.1016/j.cell.2005.08.029. hdl:11858/00-001M-0000-0010-8592-0. PMID16169070. S2CID8235923.
↑ Lehner B, Semple JI, Brown SE, Counsell D, Campbell RD, Sanderson CM (January 2004). "Analysis of a high-throughput yeast two-hybrid system and its use to predict the function of intracellular proteins encoded within the human MHC class III region". Genomics. 83 (1): 153–67. doi:10.1016/S0888-7543(03)00235-0. PMID14667819.
Maruyama K, Sugano S (1994). "Oligo-capping: a simple method to replace the cap structure of eukaryotic mRNAs with oligoribonucleotides". Gene. 138 (1–2): 171–4. doi:10.1016/0378-1119(94)90802-8. PMID8125298.
Suzuki Y, Yoshitomo-Nakagawa K, Maruyama K, etal. (1997). "Construction and characterization of a full length-enriched and a 5'-end-enriched cDNA library". Gene. 200 (1–2): 149–56. doi:10.1016/S0378-1119(97)00411-3. PMID9373149.
Lehner B, Semple JI, Brown SE, etal. (2004). "Analysis of a high-throughput yeast two-hybrid system and its use to predict the function of intracellular proteins encoded within the human MHC class III region". Genomics. 83 (1): 153–67. doi:10.1016/S0888-7543(03)00235-0. PMID14667819.
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