Characterization of human γ-tryptases, novel members of the chromosome 16p mast cell tryptase and prostasin gene families

被引:96
作者
Caughey, GH
Raymond, WW
Blount, JL
Hau, LWT
Pallaoro, M
Wolters, PJ
Verghese, GM
机构
[1] Univ Calif San Francisco, Inst Cardiovasc Res, San Francisco, CA 94143 USA
[2] Univ Calif San Francisco, Dept Med, San Francisco, CA 94143 USA
关键词
D O I
10.4049/jimmunol.164.12.6566
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Previously, this laboratory identified clusters of alpha-, beta-, and mast cell protease-7-like tryptase genes on human chromosome 16p13.3. The present work characterizes adjacent genes encoding novel serine proteases, termed gamma-tryptases, and generates a refined map of the multitryptase locus, Each gamma gene lies between an alpha 1H Ca2+ channel gene (CACNA1H) and a beta II- or beta III-tryptase gene and is similar to 30 kb from polymorphic minisatellite MS205, The tryptase locus also contains at least four tryptase-like pseudogenes, including mastin, a gene expressed in dogs but not in humans. Genomic DNA blotting results suggest that gamma I- and gamma II-tryptases are alleles at the same site, beta II- and beta III-tryptases appear to be alleles at a neighboring site, and alpha II- and beta I-tryptases appear to be alleles at a third site. gamma-Tryptases are transcribed in lung, intestine, and in several other tissues and in a mast cell line (HMC-1) that also expresses gamma-tryptase protein. Immunohistochemical analysis suggests that gamma-tryptase is expressed by airway mast cells. gamma-Tryptase catalytic domains are similar to 48% identical with those of known mast cell tryptases and possess mouse homologues. We predict that gamma-tryptases are glycosylated oligomers with tryptic substrate specificity and a distinct mode of activation. A feature not found in described tryptases is a C-terminal hydrophobic domain, which may be a membrane anchor, Although the catalytic domains contain tryptase-like features, the hydrophobic segment and intron exon organization are more closely related to another recently described protease, prostasin, In summary, this work describes gamma-tryptases, which are novel members of chromosome 16p tryptase/prostasin gene families. Their unique features suggest possibly novel functions.
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页码:6566 / 6575
页数:10
相关论文
共 47 条
  • [21] ISOLATION, CHARACTERIZATION, AND TRANSCRIPTION OF THE GENE ENCODING MOUSE MAST-CELL PROTEASE-7
    MCNEIL, HP
    REYNOLDS, DS
    SCHILLER, V
    GHILDYAL, N
    GURLEY, DS
    AUSTEN, KF
    STEVENS, RL
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1992, 89 (23) : 11174 - 11178
  • [22] CLONING AND CHARACTERIZATION OF A 2ND COMPLEMENTARY-DNA FOR HUMAN TRYPTASE
    MILLER, JS
    MOXLEY, G
    SCHWARTZ, LB
    [J]. JOURNAL OF CLINICAL INVESTIGATION, 1990, 86 (03) : 864 - 870
  • [23] CLONING AND CHARACTERIZATION OF COMPLEMENTARY-DNA FOR HUMAN TRYPTASE
    MILLER, JS
    WESTIN, EH
    SCHWARTZ, LB
    [J]. JOURNAL OF CLINICAL INVESTIGATION, 1989, 84 (04) : 1188 - 1195
  • [24] Characterization of genes encoding known and novel human mast cell tryptases on chromosome 16p13.3
    Pallaoro, M
    Fejzo, MS
    Shayesteh, L
    Blount, JL
    Caughey, GH
    [J]. JOURNAL OF BIOLOGICAL CHEMISTRY, 1999, 274 (06) : 3355 - 3362
  • [26] Human β-tryptase is a ring-like tetramer with active sites facing a central pore
    Pereira, PJB
    Bergner, A
    Macedo-Ribeiro, S
    Huber, R
    Matschiner, G
    Fritz, H
    Sommerhoff, CP
    Bode, W
    [J]. NATURE, 1998, 392 (6673) : 306 - 311
  • [27] RACK KA, 1993, AM J HUM GENET, V52, P987
  • [28] PURIFICATION AND CHARACTERIZATION OF DOG MAST-CELL PROTEASE-3, AN OLIGOMERIC RELATIVE OF TRYPTASES
    RAYMOND, WW
    TAM, EK
    BLOUNT, JL
    CAUGHEY, GH
    [J]. JOURNAL OF BIOLOGICAL CHEMISTRY, 1995, 270 (22) : 13164 - 13170
  • [29] REYNOLDS DS, 1991, J BIOL CHEM, V266, P3847
  • [30] MAST-CELL TRYPTASE IS A MITOGEN FOR CULTURED FIBROBLASTS
    RUOSS, SJ
    HARTMANN, T
    CAUGHEY, GH
    [J]. JOURNAL OF CLINICAL INVESTIGATION, 1991, 88 (02) : 493 - 499