Identification of a novel human sterol-sensitive ATP-binding cassette transporter (ABCA7)

Biochemical and Biophysical Research Communications

Volumn 273, Issue 2, 2000, Pages 532-538

  Kaminski, Wolfgang E ^a   Orsó, Evelyn ^a   Diederich, Wendy ^a   Klucken, Jochen ^a   Drobnik, Wolfgang ^a   Schmitz, Gerd ^a  

^a UNIVERSITY OF REGENSBURG   (Germany)

Author keywords

[No Author keywords available]

Indexed keywords

ABC TRANSPORTER; CARRIER PROTEIN; COMPLEMENTARY DNA; HIGH DENSITY LIPOPROTEIN; LOW DENSITY LIPOPROTEIN; MESSENGER RNA;

AMINO ACID SEQUENCE; ARTICLE; BINDING SITE; BONE MARROW; CELL DIFFERENTIATION; CONTROLLED STUDY; GENE EXPRESSION; GENE INDUCTION; HUMAN; HUMAN CELL; LEUKOCYTE; LYMPHOID TISSUE; MACROPHAGE; MONOCYTE; NONHUMAN; NUCLEOTIDE SEQUENCE; OPEN READING FRAME; PRIORITY JOURNAL; SEQUENCE HOMOLOGY; SPLEEN; THYMUS; TISSUE DISTRIBUTION;

EID: 0033890964     PISSN: 0006291X     EISSN: None     Source Type: Journal    
DOI: 10.1006/bbrc.2000.2954     Document Type: Article

References (19)

1. Higgins C. F. ABC transporters: From microorganisms to man. Annu. Rev. Cell Biol. 8:1992;67-113.
2. Klein I., Sarkadi B., Varadi A. An inventory of the human ABC proteins. Biochim. Biophys. Acta. 1461:1999;237-262.
3. Dean M., Allikmets R. Evolution of ATP-binding cassette transporter genes. Curr. Opin. Genet. Dev. 5:1995;779-785.
4. Broccardo C., Luciani M., Chimini G. The ABCA subclass of mammalian transporters. Biochim. Biophys. Acta. 1461:1999;395-404.
5. Langmann T., Klucken J., Reil M., Liebisch G., Luciani M.-F., Chimini G., Kaminski W. E., Schmitz G. Molecular cloning of the human ATP-binding cassette transporter 1 (hABC1): Evidence for sterol-dependent regulation in macrophages. Biochem. Biophys. Res. Commun. 257:1999;29-33.
6. Klucken J., Büchler C., Orsó E., Kaminski W. E., Porsch-Özcürümez M., Liebisch G., Kapinsky M., Diederich W., Drobnik W., Dean M., Allikmets R., Schmitz G. ABCG1 (ABC8), the human homolog of the Drosophila white gene, is a regulator of macrophage cholesterol and phospholipid transport. Proc. Natl. Acad. Sci. USA. 97:2000;817-822.
7. Bodzioch M., Orsó E., Klucken J., Langmann T., Böttcher A., Diederich W., Drobnik W., Barlage S., Büchler C., Porsch-Özcürümez M., Kaminski W. E., Hahmann H. W., Oette K., Rothe G., Aslanidis C., Lackner K. J., Schmitz G. The gene encoding ATP-binding cassette transporter 1 is mutated in Tangier disease. Nat. Genet. 22:1999;347-351.
8. Brooks-Wilson A., Marcil M., Clee S. M., Zhang L. H., Roomp K., van Dam M., Yu L., Brewer C., Collins J. A., Molhuizen H. O., Loubser O., Ouelette B. F., Fichter K., Ashbourne-Excoffon K. J., Sensen C. W., Scherer S., Mott S., Denis M., Martindale D., Frohlich J., Morgan K., Koop B., Pimstone S., Kastelein J. J., Genest J., Hayden M. R. Mutations in ABC1 in Tangier disease and familial high-density lipoprotein deficiency. Nat. Genet. 22:1999;336-345.
9. Rust S., Rosier M., Funke H., Real J., Amoura Z., Piette J. C., Deleuze J. F., Brewer H. B., Duverger N., Denefle P., Assmann G. Tangier disease is caused by mutations in the gene encoding ATP-binding cassette transporter 1. Nat. Genet. 22:1999;352-355.
10. Orsó E., Broccardo C., Kaminski W. E., Böttcher A., Liebisch G., Drobnik W., Götz A., Chambenoit O., Diederich W., Langmann T., Spruss T., Luciani M.-F., Rothe G., Lackner K. J., Chimini G., Schmitz G. Transport of lipids from Golgi to plasma membrane is defective in Tangier disease patients and Abc1 deficient mice. Nat. Genet. 24:2000;192-196.
11. Allikmets R., Singh N., Sun H., Shroyer N. F., Hutchinson A., Chidambaram A., Gerrard B., Baird L., Stauffer D., Peiffer A., Rattner A., Smallwood P., Li Y., Anderson K. L., Lewis R. A., Nathans J., Leppert M., Dean M., Lupski J. R. A photoreceptor cell-specific ATP-binding transporter gene (ABCR) is mutated in recessive Stargardt macular dystrophy. Nat. Genet. 15:1997;236-246.
12. Allikmets R., Shroyer N. F., Singh N., Seddon J. M., Lewis R. A., Bernstein P. S., Peiffer A., Zabriskie N. A., Li Y., Hutchinson A., Dean M., Lupski J. R., Leppert M. Mutation of the Stargardt disease gene (ABCR) in age-related macular degeneration. Science. 277:1997;1805-1807.
13. Martinez-Mir A., Paloma E., Allikmets R., Ayuso C., del Rio T., Dean M., Vilageliu L., Gonzalez-Duarte R., Balcells S. Retinitis pigmentosa caused by a homozygous mutation in the Stargardt disease gene ABCR. Nat. Genet. 18:1998;11-12.
14. Langmann T., Becker A., Aslanidis C., Notka F., Ullrich H., Schwer H., Schmitz G. Structural organization and characterization of the promoter region of a human carboxylesterase gene. Biochim. Biophys. Acta. 1350:1997;65-74.
15. Basu S. K., Goldstein J. L., Brown M. S. Characterization of the low density lipoprotein receptor in membranes prepared from human fibroblasts. J. Biol. Chem. 253:1978;3852-3856.
16. Chirgwin J. M., Przybyla A. E., MacDonald R. J., Rutter W. J. Isolation of biologically active ribonucleic acid from sources enriched in ribonuclease. Biochemistry. 18:1979;5294-5299.
17. Broccardo, C., Luciani, M.-F., Jordan, B., and Chimini, G.1999The ABC-1 like subclass of mammalian ABC transporters. Diagnostic motifs and search for novel members. Poster session, Second FEBS Advanced Lecture Course, Gosau, Austria, Feb. 20-27.
18. Vente A., Korn B., Zehetner G., Poustka A., Lehrach H. Distribution and early development of microarray technology in Europe. Nat. Genet. 22:1999;22.
19. Jung T., Schauer U., Heusser C., Neumann C., Rieger C. Detection of intracellular cytokines by flow cytometry. J. Immunol. Methods. 159:1993;197-207.