Chromosomal localization of three vacuolar-H+-ATPase 16 kDa subunit (ATP6V0C) genes in the murine genome

Cytogenetic and Genome Research

Volumn 97, Issue 1-2, 2002, Pages 111-115

  Simckes, A M ^a   Swanson, S K ^a   White, R A ^a  

^a CHILDREN S MERCY HOSPITAL   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

PROTON TRANSPORTING ADENOSINE TRIPHOSPHATASE; COMPLEMENTARY DNA; PROTEIN SUBUNIT; PROTON TRANSPORTING ADENOSINE TRIPHOSPHATE SYNTHASE;

ANIMAL TISSUE; ARTICLE; CHROMOSOMAL LOCALIZATION; CHROMOSOME MAP; CONTROLLED STUDY; GENE LOCUS; GENE STRUCTURE; GENOME ANALYSIS; HUMAN; MOLECULAR WEIGHT; MOUSE; NONHUMAN; NUCLEOTIDE SEQUENCE; PRIORITY JOURNAL; SEQUENCE HOMOLOGY; ANIMAL; C57BL MOUSE; CHEMISTRY; COMPARATIVE STUDY; GENETICS; GENOME; MURIDAE; SPECIES DIFFERENCE;

MURINAE;

ANIMALS; BASE SEQUENCE; CHROMOSOME MAPPING; DNA, COMPLEMENTARY; GENOME; HUMANS; MICE; MICE, INBRED C57BL; MOLECULAR WEIGHT; MURIDAE; PROTEIN SUBUNITS; SPECIES SPECIFICITY; VACUOLAR PROTON-TRANSLOCATING ATPASES;

EID: 0036050799     PISSN: 14248581     EISSN: None     Source Type: Journal    
DOI: 10.1159/000064065     Document Type: Article

References (41)

1. Arai H, Terres G, Pink S, Forgac M: Topography and subunit stochiometry of the coated vesicle proton pump. J biol Chem 263:8796-8802 (1988).
2. + ATPase: New Physiol Sci 16:145-151 (2001).
3. Brown D, Hirsch S, Gluck S: Localization of a proton-pumping ATPase in rat kidney. J clin Invest 82:2114-2126 (1988a).
4. +-ATPase in opposite plasma domains in kidney epithelial cell sub-populations. Nature 331:622-624 (1988b).
5. +-ATPase in cortical collecting tubules of a patient with Sjogren's syndrome and distal renal tubulal acidosis. J Am Soc Nephrol 3:261-274 (1991).
6. +-ATPase: a universal proton pump of eukaryotes. Biochem J 324:697-712 (1997).
7. Finbow ME, Harrison M, Jones P: Ductin - a proton pump component, a gap junction channel and a neurotransmitter release channel. Bioessays 17:247-255 (1995).
8. Forgac M: Structure and function of vacuolar class of ATP-driven proton pumps. Physiol Rev 69:765-796 (1989).
9. Forgac M: Structure, function and regulation of the vacuolar (H+)-ATPases. FEBS Lett 440:258-263 (1998).
10. Gillespie GA, Somlo S, Germino GG, Weinstat-Saslow D, Reeders S: CpG island in the region of an autosomal dominant polycystic kidney disease locus defines the 5′ end of a gene encoding a putative proton channel. Proc natl Acad Sci, USA 88:4289-4293 (1991).
11. +transport. J exp Biol 172:205-218 (1992).
12. +-ATPase from mouse cerebellum. Biochem biophys Res Comm 176:1062-1067 (1991).
13. +-ATPase genes: presence of four genes including pseudogenes for the 16-kDa proteolipid subunit in the human genome. Bioch biophys Res Comm 183:856-863 (1992).
14. Hayami K, Noumi T, Inoue H, Sun-Wada G, Yoshimizu T, Kanazawa H: The murine genome contains one functional gene and two pseudogenes coding for the 16 kDa proteolipid subunit of vacuolar H-Atpase. Gene 273:199-206 (2001).
15. +-ATPases with heterogeneous forms of Mr = 31,000 subunit have different membrane distributions in mammalian kidney. J biol Chem 267:9948-9957 (1992).
16. Hirsch S, Strauss A, Masood K, Lee S, Sukhatme V, Gluck S: Isolation and sequence of a cDNA clone encoding the 31-kDa subunit of bovine kidney vacuolar H(+)-ATPase. Proc natl Acad Sci, USA 85:3004-3008 (1988).
17. +-Atpase leads to early embryonic lethality. Biochim biophys Acta 1413:130-138 (1999).
18. Karet FE, Finberg KE, Nelson RD, Nayir A, Mocan H, Sanjed SA, Rodriguez-Soriano J, Santos F, Cremers CW, Di Pietro A, Hoffbrand BI, Winiarski J, Bakkaloglu A, Ozen S, Dusensel R, Goodyer P, Hulton SA, Wu DK, Skvorak AB, Morton CC, Cunningham MJ, Jha V, Lifton RP: Mutations in the gene encoding B1 subunit of H+-ATPase cause tubular acidosis with sensorineural deafness. Nature Genet 21:84-90 (1999).
19. Leiter EH, Chapman HD: Obesity-induced diabetes (diabesity) in C57BL/KsJ mice produces aberrant trans-regulation of sex steroid sulfotransferase genes. J clin Invest 93:2007-2013 (1994)
20. Li YP, Chen W, Liang Y, Li E, Stashenko P: Atp6i-deficient mice exhibit severe osteopetrosis due to loss of osteoclast-mediated extracellular acidification. Nature Genet 23:447-451 (1999).
21. Ludwig J, Kerscher S, Brandt U, Pfeiffer K, Getlawi F, Apps DK, Schagger H: Identification and characterization of a novel 9.2-kDa membrane sector-associated protein of vacuolar proton-ATPase from chromaffin granules. J biol Chem 273:10939-10947 (1998).
22. Nelson H, Mandiyan S, Noumi T, Moriyama Y, Miedel MC, Nelson N: Molecular cloning of cDNA encoding the C subunit of H+-ATPase from bovine chromaffin granules. J biol Chem 265:20390-20393 (1990).
23. Nelson N, Harvey WR: Vacuolar and plasma membrane proton-adenosine triphosphatases. Pysiol Rev 79:361-385 (1999).
24. +-ATPase 56-kilodalton subunit in renal intercalated cells. Proc natl Acad Sci, USA 89:3541-3545 (1992).
25. +-ATPases: organellar and tissue distribution of 16 kDa proteolipids. J Biochem 112:212-219 (1992).
26. Oka T, Yamamoto R, Futai M: Multiple genes for vacuolar-type ATPase proteolipid in Caenorhabditis elegans. J biol Chem 273:22570-22576 (1998).
27. Padgett RA, Grabowski PJ, Konarska MM, Seiler S, Sharp PA: Splicing of messenger RNA precursors. A Rev Biochem 55:1119-1150 (1986).
28. +-ATPase from Arabidopsis thaliana. Plant Mol Biol 29:227-244 (1995).
29. Pilz A, Glenister P, Povey S, Lyon M, Abbott C: The mouse homologue of the human tuberous sclerosis 2 (TSC2) gene maps to chromosome 17, but does not fall within the tw18 or th20 deletions. Genomics 26:420-421 (1995).
30. +-ATPase following acute unilateral obstruction in rats. Am J Physiol 261:F365-F376 (1991).
31. Roehm NW, Carbone A, Kushnir E, Taylor BA, Riblet RJ, Marrack P, Kappler JW: The major histocompatibility complex-restricted antigen receptor on T cells: the genetics of expression of an allotype. J Immunol 135:2176-2182 (1985).
32. Rowe LB, Nadeau JH, Turner R, Frankel WN, Letts VA, Eppig JT, Ko MSH, Thurston SJ, Birkenmeier EH: Maps from two interspecific backcross panels available as a community genetic mapping resource. Mammal Genome 5:253-274 (1994).
33. Smith AN, Finberg KE, Wagner CA, Lifton RP, Devonald MA, Su Y, Karet FE: Molecular cloning and characterization of Atp6n1b: a novel fourth murine vacuolar H+-ATPase a-subunit gene. J biol Chem 276:42382-42388 (2001).
34. Smith AN, Skaug J, Choate KA, Nayir A, Bakkaloglu A, Ozen S, Hulton SA, Sanjad SA, Al-Sabban EA, Li Scherer SW, Karet FE: Mutations in ATP6N1B, encoding a new kidney vacuolar proton pump 116-kDa subunit, cause recessive distal renal tubular acidosis with preserved hearing. Nature Genet 26:71-75 (2000).
35. Sun-Wada G, Murata Y, Yamamom A, Kanazawa H, Wada Y, Futai M: Acid endomembrane organelles are required for mouse post-implantation development. Dev Biol 228:315-325 (2000).
36. Suzuki Y, Tsutsumi Y, Nakagawa M, Suzuki H, Matsushita K, Beppu M, Aoki H, Ichikawa Y, Mizushima Y: Osteoclast-like cells in an in vitro model of bone destruction by rheumatoid synovium. Rheumatology 40:673-682 (2001).
37. Swank RT, Reddington M, Howlett O, Novak, EN: Platelet storage pool deficiency associated with inherited abnormalities of the inner ear in the mouse pigment mutants muted and mocha. Blood 78:2036-2044 (1991).
38. +-ATPase. Biochem biophys Res Comm 197:15-21 (1993).
39. +-ATPase: differential expression of two human subunit B isoforms. Biochem J 303:191-198 (1994).
40. van Hille, B, Richener, H, Green JR, Bilbe G: The ubiquitous VA68 isoform of subunit A of the vacuolar H(+)-ATPase is highly expressed in human osteoclasts. Biochem biophys Res Commun 214:1108-1113 (1995).
41. White RA, Peters LL, Adkison LR, Korsgren C, Cohen CM, Lux SE: The murine pallid mutation is a platelet storage pool disease associated with the protein 4.2 (pallidin) gene. Nature Genet 2:80-83 (1992).