Complete coding sequence, promoter region, and genomic structure of the human ABCA2 gene and evidence for sterol-dependent regulation in macrophages

Biochemical and Biophysical Research Communications

Volumn 281, Issue 1, 2001, Pages 249-258

  Kaminski, Wolfgang E ^a   Piehler, Armin ^a   Püllmann, Kerstin ^a   Porsch Özcürümez, Mustafa ^a   Duong, Chinh ^a   Bared, Guido Maa ^a   Büchler, Christa ^a   Schmitz, Gerd ^a  

^a UNIVERSITY OF REGENSBURG   (Germany)

Author keywords

[No Author keywords available]

Indexed keywords

ABC TRANSPORTER; ABC TRANSPORTER A2; MESSENGER RNA; UNCLASSIFIED DRUG;

ARTICLE; BINDING SITE; CELL CULTURE; DNA SEQUENCE; GENE AMPLIFICATION; GENE EXPRESSION; GENE STRUCTURE; HUMAN; HUMAN CELL; MACROPHAGE; NUCLEOTIDE SEQUENCE; PRIORITY JOURNAL; PROMOTER REGION; STEROL METABOLISM;

EID: 0034815432     PISSN: 0006291X     EISSN: None     Source Type: Journal    
DOI: 10.1006/bbrc.2001.4305     Document Type: Article

References (39)

1. ABC transporters: From microorganisms to man
2. Inventory and function of yeast ABC proteins: About sex, stress, pleiotropic drug and heavy metal resistance
3. An inventory of the human ABC proteins
4. MDR1 p-glycoprotein is a lipid translocase of broad specificity, while MDR3 p-glycoprotein specifically translocates phosphatidylcholine
5. ABCG1 (ABC8), the human homolog of the Drosophila white gene, is a regulator of macrophage cholesterol and phospholipid transport
6. ABC transporters in cellular lipid trafficking
7. The gene encoding ATP-binding cassette transporter 1 is mutated in Tangier disease
8. Mutations in ABC1 in Tangier disease and familial high-density lipoprotein deficiency
9. Tangier disease is caused by mutations in the gene encoding ATP-binding cassette transporter 1
10. Transport of lipids from Golgi to plasma membrane is defective in Tangier disease patients and Abc1 deficient mice
11. Cloning of two novel ABC transporters mapping on human chromosome 9
12. Cloning, characterization and tissue distribution of the rat ATP-binding cassette (ABC) transporter ABC2/ABCA2
13. Amplification of the ATP-binding cassette 2 transporter gene is functionally linked with enhanced efflux of estramustine in ovarian carcinoma cells
14. Complement and atherogenesis: Binding of CRP to degraded, nonoxidized LDL enhances complement activation
15. Identification of a novel human sterol-sensitive ATP-binding cassette transporter (ABCA7)
16. Isolation of human promoter regions by Alu repeat consensus-based polymerase chain reaction
17. Genomic organization of the human cholesterol-responsive ABC transporter ABCA7: Tandem linkage with the minor histocompatibility antigen HA-1 gene
18. Sequence identification of 2, 375 human brain genes
19. Prediction of the coding sequences of unidentified human genes. XIV. The complete sequences of 100 new cDNA clones from brain which code for large proteins in vitro
20. Molecular cloning of the human ATP-binding cassette transporter 1 (hABC1): Evidence for sterol-dependent regulation in macrophages
21. Human ATP-binding cassette transporter 1 (ABC1): Genomic organization and identification of the genetic defect in the original Tangier disease kindred
22. Organization and expression of eucaryotic split genes coding for proteins
23. Structure of the human MDR3 gene and physical mapping of the human MDR locus
24. Identification of the cystic fibrosis gene: Chromosome walking and jumping
25. Transcription factors, normal myeloid development, and leukemia
26. Developmental expression of Sp1 in the mouse
27. Expression patterns of the four nuclear factor I genes during mouse embryogenesis indicate a potential role in development
28. Identification of NFI-binding sites and cloning of NFI-cDNAs suggest a regulatory role for NFI transcription factors in olfactory neuron gene expression
29. The Wilms’ tumor gene product WT1 mediates the down-regulation of the rat epidermal growth factor receptor by nerve growth factor in PC12 cells
30. Molecular characterization of cDNA encoding a novel protein related to transcriptional enhancer factor-1 from neural precursor cells
31. Molecular cloning, sequencing, and mapping of EGR2, a human early growth response gene encoding a protein with "zinc-binding finger" structure
32. Disruption of Krox-20 results in alteration of rhombomeres 3 and 5 in the developing hindbrain
33. Mutations in the early growth response 2 (EGR2) gene are associated with hereditary myelinopathies
34. Novel missense mutation in the early growth response 2 gene associated with a Dejerine-Sottas syndrome phenotype
35. EGR3, a novel member of the Egr family of genes encoding immediate-early transcription factors
36. Sensory ataxia and muscle spindle agenesis in mice lacking the transcription factor Egr3
37. Complete genomic sequence of the human ABCA1 gene: Analysis of the human and mouse ATP-binding cassette A promoter
38. A photoreceptor cell-specific ATP-binding transporter gene (ABCR) is mutated in recessive Stargardt macular dystrophy
39. Organization of the AB CR gene: Analysis of promoter and splice junction sequences