Cloning of the TMPRSS2 gene, which encodes a novel serine protease with transmembrane, LDLRA, and SRCR domains and maps to 21q22.3

被引:194
作者
PaoloniGiacobino, A
Chen, HM
Peitsch, MC
Rossier, C
Antonarakis, SE
机构
[1] UNIV GENEVA,SCH MED,DEPT GENET & MICROBIOL,LAB HUMAN MOL GENET,CH-1211 GENEVA,SWITZERLAND
[2] GLAXO INST MOL BIOL SA,CH-1211 GENEVA,SWITZERLAND
[3] HOP CANTONAL GENEVA,DIV MED GENET,CH-1211 GENEVA,SWITZERLAND
关键词
D O I
10.1006/geno.1997.4845
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
To contribute to the development of the transcription map of human chromosome 21 (HC21), we have used exon trapping from pools of HC21-specific cosmids. Using selected trapped exons, we have identified a novel gene (named TMPRSS2) that encodes a multimeric protein with a serine protease domain. The TMPRSS2 3.8-kb mRNA is expressed strongly in small intestine and weakly in several other tissues. The full-length cDNA encodes a predicted protein of 492 amino acids that contains the following domains: (i) A serine protease domain (aa 255-492) of the S1 family that probably cleaves at Arg or Lys residues. (ii) An SRCR (scavenger receptor cysteine-rich) domain (aa 149-242) of group A (6 conserved Cys). This type of domain is involved in the binding to other cell surface or extracellular molecules. (iii) An LDLRA (LDL receptor class A) domain (aa 113-148). This type of domain forms a binding site for calcium. (iv) A predicted transmembrane domain (aa 84-106). No typical signal peptide was recognized. The gene was mapped to 21q22.3 between markers ERG and D21S56 in the same P1 as MX1. The physiological role of TMPRSS2 and its involve ment in trisomy 21 phenotypes or monogenic disorders that map to HC21 are unknown. (C) 1997 Academic Press.
引用
收藏
页码:309 / 320
页数:12
相关论文
共 43 条
  • [1] AN AUTOSOMAL LOCUS CAUSING AUTOIMMUNE-DISEASE - AUTOIMMUNE POLYGLANDULAR DISEASE TYPE-I ASSIGNED TO CHROMOSOME-21
    AALTONEN, J
    BJORSES, P
    SANDKUIJL, L
    PERHEENTUPA, J
    PELTONEN, L
    [J]. NATURE GENETICS, 1994, 8 (01) : 83 - 87
  • [2] ALTSCHUL SF, 1990, J MOL BIOL, V215, P403, DOI 10.1006/jmbi.1990.9999
  • [3] HUMAN CHROMOSOME-21 - GENOME MAPPING AND EXPLORATION, CIRCA 1993
    ANTONARAKIS, SE
    [J]. TRENDS IN GENETICS, 1993, 9 (04) : 142 - 148
  • [4] BonneTamir B, 1996, AM J HUM GENET, V58, P1254
  • [5] EXON AMPLIFICATION - A STRATEGY TO ISOLATE MAMMALIAN GENES BASED ON RNA SPLICING
    BUCKLER, AJ
    CHANG, DD
    GRAW, SL
    BROOK, JD
    HABER, DA
    SHARP, PA
    HOUSMAN, DE
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1991, 88 (09) : 4005 - 4009
  • [6] Cloning of 559 potential exons of genes of human chromosome 21 by exon trapping
    Chen, H
    Chrast, R
    Rossier, C
    Morris, MA
    Lalioti, MD
    Antonarakis, SE
    [J]. GENOME RESEARCH, 1996, 6 (08): : 747 - 760
  • [7] ISOLATION AND MAPPING OF HUMAN-CHROMOSOME-21 CDNA - PROGRESS IN CONSTRUCTING A CHROMOSOME-21 EXPRESSION MAP
    CHENG, JF
    BOYARTCHUK, V
    ZHU, YW
    [J]. GENOMICS, 1994, 23 (01) : 75 - 84
  • [8] CONTINUUM OF OVERLAPPING CLONES SPANNING THE ENTIRE HUMAN CHROMOSOME-21Q
    CHUMAKOV, I
    RIGAULT, P
    GUILLOU, S
    OUGEN, P
    BILLAUT, A
    GUASCONI, G
    GERVY, P
    LEGALL, I
    SOULARUE, P
    GRINAS, L
    BOUGUELERET, L
    BELLANNECHANTELOT, C
    LACROIX, B
    BARILLOT, E
    GESNOUIN, P
    POOK, S
    VAYSSEIX, G
    FRELAT, G
    SCHMITZ, A
    SAMBUCY, JL
    BOSCH, A
    ESTIVILL, X
    WEISSENBACH, J
    VIGNAL, A
    RIETHMAN, H
    COX, D
    PATTERSON, D
    GARDINER, K
    HATTORI, M
    SAKAKI, Y
    ICHIKAWA, H
    OHKI, M
    LEPASLIER, D
    HEILIG, R
    ANTONARAKIS, S
    COHEN, D
    [J]. NATURE, 1992, 359 (6394) : 380 - 387
  • [9] ISOLATION OF GENES FROM COMPLEX SOURCES OF MAMMALIAN GENOMIC DNA USING EXON AMPLIFICATION
    CHURCH, DM
    STOTLER, CJ
    RUTTER, JL
    MURRELL, JR
    TROFATTER, JA
    BUCKLER, AJ
    [J]. NATURE GENETICS, 1994, 6 (01) : 98 - 105
  • [10] DALY NL, 1995, P NATL ACAD SCI USA, V92, P63334