[{"@context":"http:\/\/schema.org\/","@type":"BlogPosting","@id":"https:\/\/wiki.edu.vn\/en\/wiki24\/carbonic-anhydrase-12-wikipedia\/#BlogPosting","mainEntityOfPage":"https:\/\/wiki.edu.vn\/en\/wiki24\/carbonic-anhydrase-12-wikipedia\/","headline":"Carbonic anhydrase 12 – Wikipedia","name":"Carbonic anhydrase 12 – Wikipedia","description":"before-content-x4 From Wikipedia, the free encyclopedia after-content-x4 Protein-coding gene in the species Homo sapiens This article is about the enzyme.","datePublished":"2016-09-26","dateModified":"2016-09-26","author":{"@type":"Person","@id":"https:\/\/wiki.edu.vn\/en\/wiki24\/author\/lordneo\/#Person","name":"lordneo","url":"https:\/\/wiki.edu.vn\/en\/wiki24\/author\/lordneo\/","image":{"@type":"ImageObject","@id":"https:\/\/secure.gravatar.com\/avatar\/c9645c498c9701c88b89b8537773dd7c?s=96&d=mm&r=g","url":"https:\/\/secure.gravatar.com\/avatar\/c9645c498c9701c88b89b8537773dd7c?s=96&d=mm&r=g","height":96,"width":96}},"publisher":{"@type":"Organization","name":"Enzyklop\u00e4die","logo":{"@type":"ImageObject","@id":"https:\/\/wiki.edu.vn\/wiki4\/wp-content\/uploads\/2023\/08\/download.jpg","url":"https:\/\/wiki.edu.vn\/wiki4\/wp-content\/uploads\/2023\/08\/download.jpg","width":600,"height":60}},"image":{"@type":"ImageObject","@id":"https:\/\/upload.wikimedia.org\/wikipedia\/commons\/thumb\/6\/63\/Journal_Icon.svg\/20px-Journal_Icon.svg.png","url":"https:\/\/upload.wikimedia.org\/wikipedia\/commons\/thumb\/6\/63\/Journal_Icon.svg\/20px-Journal_Icon.svg.png","height":"18","width":"20"},"url":"https:\/\/wiki.edu.vn\/en\/wiki24\/carbonic-anhydrase-12-wikipedia\/","about":["Wiki"],"wordCount":10235,"articleBody":"     (adsbygoogle = window.adsbygoogle || []).push({});before-content-x4From Wikipedia, the free encyclopedia       (adsbygoogle = window.adsbygoogle || []).push({});after-content-x4Protein-coding gene in the species Homo sapiensThis article is about the enzyme. For other uses, see CA-12.Carbonic anhydrase 12 is an enzyme that in humans is encoded by the CA12 gene.[5][6]       (adsbygoogle = window.adsbygoogle || []).push({});after-content-x4Table of ContentsFunction[edit]Pathology[edit]Molecular Basis of Cystic Fibrosis-like Syndrome[edit]High Impact Information on CAXII[edit]Analytical, Diagnostic, and Therapeutic Context of CAXII[edit]References[edit]External links[edit]Further reading[edit]Function[edit]Carbonic anhydrases (CAs) are a large family of zinc metalloenzymes that catalyze the reversible hydration of carbon dioxide. They participate in a variety of biological processes, including respiration, calcification, acid-base balance, bone resorption, and the formation of aqueous humor, cerebrospinal fluid, saliva, and gastric acid. This gene product is a type I membrane protein that is highly expressed in normal tissues, such as kidney, colon and pancreas, and has been found to be overexpressed in 10% of clear cell renal carcinomas. Two transcript variants encoding different isoforms have been identified for this gene.[6]Pathology[edit]Loss of function mutations in the CAXII gene result in defects in fluids and carbonate secretions in the following diseases:       (adsbygoogle = window.adsbygoogle || []).push({});after-content-x41) Cystic fibrosis-like syndrome with normal cystic fibrosis transmembrane conductance regulator (CFTR) protein levels [7][8][9][10][11][12]2) Pancreatitis[13][14]3) Sj\u00f6gren’s syndrome[14][15]4) Xerostomia or dry mouth syndrome[9][10][11]Molecular Basis of Cystic Fibrosis-like Syndrome[edit]CAXII, with either the His121Gln or Glu143Lys mutation, localizes to basolateral membranes of polarized MDCK cells similar to the wild type enzyme, indicating no deleterious effect on subcellular location.[14]The Glu143Lys (E143K) loss-of-function variant of the CAXII gene is associated with a rare autosomal recessive condition named isolated hyperchlorhidrosis (carbonic anhydrase XII deficiency). Typically, this variant results in excessive sodium chloride loss, usually through sweating, and presents pathologically as episodic hyponatremic dehydration with bouts of vomiting and\/or diarrhoea.Generally, CAXII mutant enzymes show reduced activity. These observations make it difficult to explain the mechanism for the autosomal recessive disorder of hyponatremia, causing salt wasting in sweat due to mutant CAXII.[7][8]In a separate study, researchers observed that mutant enzyme activity is completely reduced at physiological concentrations of sodium chloride.[14] Thus, loss of the function of CAXII in sweat glands and lungs is the molecular basis for cystic fibrosis patients with normal CFTR levels.[14]High Impact Information on CAXII[edit]Differential modulation of the active site environment of CAXII by cationic quantum dots and polylysine helps design CAXII specific activators and inhibitors of the enzyme.[16] CAXII specific inhibition provides a tool to interfere with cell proliferation, resulting in cell apoptosis in T-cell lymphomas.[17]Analytical, Diagnostic, and Therapeutic Context of CAXII[edit]Serum CAXII levels should be applicable as a sero-diagnostic marker for lung cancer.[18]References[edit]^ a b c GRCh38: Ensembl release 89: ENSG00000074410 – Ensembl, May 2017^ a b c GRCm38: Ensembl release 89: ENSMUSG00000032373 – Ensembl, May 2017^ “Human PubMed Reference:”. National Center for Biotechnology Information, U.S. National Library of Medicine.^ “Mouse PubMed Reference:”. National Center for Biotechnology Information, U.S. National Library of Medicine.^ T\u00fcreci O, Sahin U, Vollmar E, Siemer S, G\u00f6ttert E, Seitz G, Parkkila AK, Shah GN, Grubb JH, Pfreundschuh M, Sly WS (Aug 1998). “Human carbonic anhydrase XII: cDNA cloning, expression, and chromosomal localization of a carbonic anhydrase gene that is overexpressed in some renal cell cancers”. Proc Natl Acad Sci U S A. 95 (13): 7608\u20137613. Bibcode:1998PNAS…95.7608T. doi:10.1073\/pnas.95.13.7608. PMC\u00a022698. PMID\u00a09636197.^ a b “Entrez Gene: CA12 carbonic anhydrase XII”.^ a b Feldshtein, M; Elkrinawi, S; Yerushalmi, B; Marcus, B; Vullo, D; Romi, H; Ofir, R; Landau, D; Sivan, S; Supuran, CT; Birk, OS (12 November 2010). “Hyperchlorhidrosis caused by homozygous mutation in CA12, encoding carbonic anhydrase XII”. American Journal of Human Genetics. 87 (5): 713\u201320. doi:10.1016\/j.ajhg.2010.10.008. PMC\u00a02978943. PMID\u00a021035102.^ a b Muhammad, E; Leventhal, N; Parvari, G; Hanukoglu, A; Hanukoglu, I; Chalifa-Caspi, V; Feinstein, Y; Weinbrand, J; Jacoby, H; Manor, E; Nagar, T; Beck, JC; Sheffield, VC; Hershkovitz, E; Parvari, R (April 2011). “Autosomal recessive hyponatremia due to isolated salt wasting in sweat associated with a mutation in the active site of Carbonic Anhydrase 12”. Human Genetics. 129 (4): 397\u2013405. doi:10.1007\/s00439-010-0930-4. PMID\u00a021184099. S2CID\u00a011034371.^ a b Hong, JH; Muhammad, E; Zheng, C; Hershkovitz, E; Alkrinawi, S; Loewenthal, N; Parvari, R; Muallem, S (15 December 2015). “Essential role of carbonic anhydrase XII in secretory gland fluid and HCO3 (-) secretion revealed by disease causing human mutation”. The Journal of Physiology. 593 (24): 5299\u2013312. doi:10.1113\/jp271378. PMC\u00a04704518. PMID\u00a026486891.^ a b Lee, M; Vecchio-Pag\u00e1n, B; Sharma, N; Waheed, A; Li, X; Raraigh, KS; Robbins, S; Han, ST; Franca, AL; Pellicore, MJ; Evans, TA; Arcara, KM; Nguyen, H; Luan, S; Belchis, D; Hertecant, J; Zabner, J; Sly, WS; Cutting, GR (23 February 2016). “Loss of carbonic anhydrase XII function in individuals with elevated sweat chloride concentration and pulmonary airway disease”. Human Molecular Genetics. 25 (10): 1923\u20131933. doi:10.1093\/hmg\/ddw065. PMC\u00a05062583. PMID\u00a026911677.^ a b Purkerson, JM; Schwartz, GJ (January 2007). “The role of carbonic anhydrases in renal physiology”. Kidney International. 71 (2): 103\u201315. doi:10.1038\/sj.ki.5002020. PMID\u00a017164835.^ Quinton, PM (December 2010). “Role of epithelial HCO3\u2212 transport in mucin secretion: lessons from cystic fibrosis”. American Journal of Physiology. Cell Physiology. 299 (6): C1222\u201333. doi:10.1152\/ajpcell.00362.2010. PMC\u00a03006319. PMID\u00a020926781.^ Kivel\u00e4, AJ; Parkkila, S; Saarnio, J; Karttunen, TJ; Kivel\u00e4, J; Parkkila, AK; Pastorekov\u00e1, S; Pastorek, J; Waheed, A; Sly, WS; Rajaniemi, H (September 2000). “Expression of transmembrane carbonic anhydrase isoenzymes IX and XII in normal human pancreas and pancreatic tumours”. Histochemistry and Cell Biology. 114 (3): 197\u2013204. doi:10.1007\/s004180000181. PMID\u00a011083462. S2CID\u00a022170460.^ a b c d e Lee, MG; Ohana, E; Park, HW; Yang, D; Muallem, S (January 2012). “Molecular mechanism of pancreatic and salivary gland fluid and HCO3 secretion”. Physiological Reviews. 92 (1): 39\u201374. doi:10.1152\/physrev.00011.2011. PMC\u00a03667394. PMID\u00a022298651.^ Almst\u00e5hl, A; Wikstr\u00f6m, M (May 2003). “Electrolytes in stimulated whole saliva in individuals with hyposalivation of different origins”. Archives of Oral Biology. 48 (5): 337\u201344. doi:10.1016\/s0003-9969(02)00200-5. PMID\u00a012711377.^ Manokaran, S; Zhang, X; Chen, W; Srivastava, DK (June 2010). “Differential modulation of the active site environment of human carbonic anhydrase XII by cationic quantum dots and polylysine”. Biochimica et Biophysica Acta (BBA) – Proteins and Proteomics. 1804 (6): 1376\u201384. doi:10.1016\/j.bbapap.2010.02.014. PMC\u00a03181075. PMID\u00a020215053.^ Lounnas, N; Rosilio, C; Nebout, M; Mary, D; Griessinger, E; Neffati, Z; Chiche, J; Spits, H; Hagenbeek, TJ; Asnafi, V; Poulsen, SA; Supuran, CT; Peyron, JF; Imbert, V (1 June 2013). “Pharmacological inhibition of carbonic anhydrase XII interferes with cell proliferation and induces cell apoptosis in T-cell lymphomas”. Cancer Letters. 333 (1): 76\u201388. doi:10.1016\/j.canlet.2013.01.020. PMID\u00a023348702.^ Kobayashi, M; Matsumoto, T; Ryuge, S; Yanagita, K; Nagashio, R; Kawakami, Y; Goshima, N; Jiang, SX; Saegusa, M; Iyoda, A; Satoh, Y; Masuda, N; Sato, Y (2012). “CAXII Is a sero-diagnostic marker for lung cancer”. PLOS ONE. 7 (3): e33952. Bibcode:2012PLoSO…733952K. doi:10.1371\/journal.pone.0033952. PMC\u00a03306309. PMID\u00a022439015.External links[edit]Further reading[edit]Sahin U, T\u00fcreci O, Schmitt H, Cochlovius B, Johannes T, Schmits R, Stenner F, Luo G, Schobert I, Pfreundschuh M (1996). “Human neoplasms elicit multiple specific immune responses in the autologous host”. Proc. Natl. Acad. Sci. U.S.A. 92 (25): 11810\u201311813. Bibcode:1995PNAS…9211810S. doi:10.1073\/pnas.92.25.11810. PMC\u00a040492. PMID\u00a08524854.Ivanov SV, Kuzmin I, Wei MH, Pack S, Geil L, Johnson BE, Stanbridge EJ, Lerman MI (1998). “Down-regulation of transmembrane carbonic anhydrases in renal cell carcinoma cell lines by wild-type von Hippel-Lindau transgenes”. Proc. Natl. Acad. Sci. U.S.A. 95 (21): 12596\u201312601. Bibcode:1998PNAS…9512596I. doi:10.1073\/pnas.95.21.12596. PMC\u00a022876. PMID\u00a09770531.Fujikawa-Adachi K, Nishimori I, Taguchi T, Onishi S (1999). “Human carbonic anhydrase XIV (CA14): cDNA cloning, mRNA expression, and mapping to chromosome 1”. Genomics. 61 (1): 74\u201381. doi:10.1006\/geno.1999.5938. PMID\u00a010512682.Karhumaa P, Parkkila S, T\u00fcreci O, Waheed A, Grubb JH, Shah G, Parkkila A, Kaunisto K, Tapanainen J, Sly WS, Rajaniemi H (2000). “Identification of carbonic anhydrase XII as the membrane isozyme expressed in the normal human endometrial epithelium”. Mol. Hum. Reprod. 6 (1): 68\u201374. doi:10.1093\/molehr\/6.1.68. PMID\u00a010611263.Kivel\u00e4 A, Parkkila S, Saarnio J, Karttunen TJ, Kivel\u00e4 J, Parkkila AK, Waheed A, Sly WS, Grubb JH, Shah G, T\u00fcreci O, Rajaniemi H (2000). “Expression of a novel transmembrane carbonic anhydrase isozyme XII in normal human gut and colorectal tumors”. Am. J. Pathol. 156 (2): 577\u201384. doi:10.1016\/S0002-9440(10)64762-1. PMC\u00a01850052. PMID\u00a010666387.Kivel\u00e4 AJ, Parkkila S, Saarnio J, Karttunen TJ, Kivel\u00e4 J, Parkkila AK, Pastorekov\u00e1 S, Pastorek J, Waheed A, Sly WS, Rajaniemi H (2001). “Expression of transmembrane carbonic anhydrase isoenzymes IX and XII in normal human pancreas and pancreatic tumours”. Histochem. Cell Biol. 114 (3): 197\u2013204. doi:10.1007\/s004180000181. PMID\u00a011083462. S2CID\u00a022170460.Parkkila S, Parkkila AK, Saarnio J, Kivel\u00e4 J, Karttunen TJ, Kaunisto K, Waheed A, Sly WS, T\u00fcreci O, Virtanen I, Rajaniemi H (2001). “Expression of the membrane-associated carbonic anhydrase isozyme XII in the human kidney and renal tumors”. J. Histochem. Cytochem. 48 (12): 1601\u20138. doi:10.1177\/002215540004801203. PMID\u00a011101628.Wykoff CC, Beasley N, Watson PH, Campo L, Chia SK, English R, Pastorek J, Sly WS, Ratcliffe P, Harris AL (2001). “Expression of the hypoxia-inducible and tumor-associated carbonic anhydrases in ductal carcinoma in situ of the breast”. Am. J. Pathol. 158 (3): 1011\u20139. doi:10.1016\/S0002-9440(10)64048-5. PMC\u00a01850356. PMID\u00a011238049.Karhumaa P, Kaunisto K, Parkkila S, Waheed A, Pastorekov\u00e1 S, Pastorek J, Sly WS, Rajaniemi H (2001). “Expression of the transmembrane carbonic anhydrases, CA IX and CA XII, in the human male excurrent ducts”. Mol. Hum. Reprod. 7 (7): 611\u2013616. doi:10.1093\/molehr\/7.7.611. PMID\u00a011420383.Whittington DA, Waheed A, Ulmasov B, Shah GN, Grubb JH, Sly WS, Christianson DW (2001). “Crystal structure of the dimeric extracellular domain of human carbonic anhydrase XII, a bitopic membrane protein overexpressed in certain cancer tumor cells”. Proc. Natl. Acad. Sci. U.S.A. 98 (17): 9545\u20139550. Bibcode:2001PNAS…98.9545W. doi:10.1073\/pnas.161301298. PMC\u00a055489. PMID\u00a011493685.Kivela AJ, Saarnio J, Karttunen TJ, Kivel\u00e4 J, Parkkila AK, Pastorekova S, Pastorek J, Waheed A, Sly WS, Parkkila TS, Rajaniemi H (2001). “Differential expression of cytoplasmic carbonic anhydrases, CA I and II, and membrane-associated isozymes, CA IX and XII, in normal mucosa of large intestine and in colorectal tumors”. Dig. Dis. Sci. 46 (10): 2179\u20132186. doi:10.1023\/A:1011910931210. PMID\u00a011680594. S2CID\u00a040928937.Liao SY, Ivanov S, Ivanova A, Ghosh S, Cote MA, Keefe K, Coca-Prados M, Stanbridge EJ, Lerman MI (2003). “Expression of cell surface transmembrane carbonic anhydrase genes CA9 and CA12 in the human eye: overexpression of CA12 (CAXII) in glaucoma”. J. Med. Genet. 40 (4): 257\u2013261. doi:10.1136\/jmg.40.4.257. PMC\u00a01735430. PMID\u00a012676895.Leppilampi M, Saarnio J, Karttunen TJ, Kivel\u00e4 J, Pastorekov\u00e1 S, Pastorek J, Waheed A, Sly WS, Parkkila S (2003). “Carbonic anhydrase isozymes IX and XII in gastric tumors”. World J. Gastroenterol. 9 (7): 1398\u2013403. doi:10.3748\/wjg.v9.i7.1398. PMC\u00a04615471. PMID\u00a012854129.Kyll\u00f6nen MS, Parkkila S, Rajaniemi H, Waheed A, Grubb JH, Shah GN, Sly WS, Kaunisto K (2003). “Localization of carbonic anhydrase XII to the basolateral membrane of H+-secreting cells of mouse and rat kidney”. J. Histochem. Cytochem. 51 (9): 1217\u201324. doi:10.1177\/002215540305100912. PMID\u00a012923247.Tarun AS, Bryant B, Zhai W, Solomon C, Shusterman D (2004). “Gene expression for carbonic anhydrase isoenzymes in human nasal mucosa”. Chem. Senses. 28 (7): 621\u2013629. doi:10.1093\/chemse\/bjg054. PMID\u00a014578124.Kivela AJ, Parkkila S, Saarnio J, Karttunen TJ, Kivela J, Parkkila AK, Bartosova M, Mucha V, Novak M, Waheed A, Sly WS, Rajaniemi H, Pastorekova S, Pastorek J (2005). “Expression of von Hippel-Lindau tumor suppressor and tumor-associated carbonic anhydrases IX and XII in normal and neoplastic colorectal mucosa”. World J. Gastroenterol. 11 (17): 2616\u201325. doi:10.3748\/wjg.v11.i17.2616. PMC\u00a04305753. PMID\u00a015849821.PDB gallery1jcz: CRYSTAL STRUCTURE OF THE EXTRACELLULAR DOMAIN OF HUMAN CARBONIC ANHYDRASE XII1jd0: CRYSTAL STRUCTURE OF THE EXTRACELLULAR DOMAIN OF HUMAN CARBONIC ANHYDRASE XII COMPLEXED WITH ACETAZOLAMIDE       (adsbygoogle = window.adsbygoogle || []).push({});after-content-x4"},{"@context":"http:\/\/schema.org\/","@type":"BreadcrumbList","itemListElement":[{"@type":"ListItem","position":1,"item":{"@id":"https:\/\/wiki.edu.vn\/en\/wiki24\/#breadcrumbitem","name":"Enzyklop\u00e4die"}},{"@type":"ListItem","position":2,"item":{"@id":"https:\/\/wiki.edu.vn\/en\/wiki24\/carbonic-anhydrase-12-wikipedia\/#breadcrumbitem","name":"Carbonic anhydrase 12 – Wikipedia"}}]}]