Genomic structure, chromosomal localization, start of transcription, and tissue expression of the human p40-phox, a new component of the nicotinamide adenine dinucleotide phosphate-oxidase complex

被引:62
作者
Zhan, SX
Vazquez, N
Zhan, SL
Wientjes, FB
Budarf, ML
Schrock, E
Ried, T
Green, ED
Chanock, SJ
机构
[1] NCI, PEDIAT BRANCH, NATL CTR HUMAN GENOME RES, NIH, BETHESDA, MD 20892 USA
[2] UCL, DIV MOL MED, LONDON, ENGLAND
[3] CHILDRENS HOSP PHILADELPHIA, DIV HUMAN GENET & MOL BIOL, PHILADELPHIA, PA 19104 USA
关键词
D O I
10.1182/blood.V88.7.2714.bloodjournal8872714
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
p40-phox is a newly isolated cytosolic component of the nicotinamide adenine dinucleotide phosphate (NADPH)-oxidase that copurifies with p87-phox, Although its function is not well defined, preliminary evidence indicates that it is a component of the cytosolic complex. We report the characterization of the human p40-phox gene, which is single copy and spans approximately 18 kb with 10 exons. Based on fluorescent in situ hybridization (FISH) studies and analysis of somatic hybrid cell lines, the chromosomal location of p40-phox is human chromosome 22q13.1. The start of transcription has been mapped to bp -156. The expression of p40-phox message is restricted to hematopoietic cells. In addition to identifying the mRNA transcript on Northern blot analysis in cells known to express components of the NADPH-oxidase, polymorphonuclear leukocytes, monocytes, B lymphoblastoid cell lines, and eosinophils, p40-phox is also expressed in two other cell types of white cell lineage, mast cells, and basophils. In addition, the mRNA for p40-phox is expressed in megakaryocytic cells, but not in erythroid cells. (C) 1996 by The American Society of Hematology.
引用
收藏
页码:2714 / 2721
页数:8
相关论文
共 57 条
  • [1] ABO A, 1992, J BIOL CHEM, V267, P16767
  • [2] ACTIVATION OF THE NADPH OXIDASE INVOLVES THE SMALL GTP-BINDING PROTEIN P21RAC1
    ABO, A
    PICK, E
    HALL, A
    TOTTY, N
    TEAHAN, CG
    SEGAL, AW
    [J]. NATURE, 1991, 353 (6345) : 668 - 670
  • [3] ARNOLD N, 1992, TECHNIQUES METHODS M, P324
  • [4] ACTIVATION OF NEUTROPHIL LEUKOCYTES - CHEMOATTRACTANT RECEPTORS AND RESPIRATORY BURST
    BAGGIOLINI, M
    BOULAY, F
    BADWEY, JA
    CURNUTTE, JT
    [J]. FASEB JOURNAL, 1993, 7 (11) : 1004 - 1010
  • [5] PHYSICAL LOCATION OF THE HUMAN-IMMUNOGLOBULIN LAMBDA-LIKE GENES, 14.1, 16.1, AND 16.2
    BAUER, TR
    MCDERMID, HE
    BUDARF, ML
    VANKEUREN, ML
    BLOMBERG, BB
    [J]. IMMUNOGENETICS, 1993, 38 (06) : 387 - 399
  • [6] BELL CJ, 1995, HUM MOL GENET, V4, P59
  • [7] BLOM T, 1992, EUR J IMMUNOL, V37, P203
  • [8] BUDARF M, 1989, AM J HUM GENET, V45, P128
  • [9] ESTABLISHMENT OF AN IMMATURE MAST-CELL LINE FROM A PATIENT WITH MAST-CELL LEUKEMIA
    BUTTERFIELD, JH
    WEILER, D
    DEWALD, G
    GLEICH, GJ
    [J]. LEUKEMIA RESEARCH, 1988, 12 (04) : 345 - 355
  • [10] AUTOSOMAL RECESSIVE CHRONIC GRANULOMATOUS-DISEASE CAUSED BY DELETION AT A DINUCLEOTIDE REPEAT
    CASIMIR, CM
    BUGHANIM, HN
    RODAWAY, ARF
    BENTLEY, DL
    ROWE, P
    SEGAL, AW
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1991, 88 (07) : 2753 - 2757