Structure of the human carboxypeptidase M gene. Identification of a proximal GC-rich promoter and a unique distal promoter that consists of repetitive elements

被引:12
作者
Li, JQ
Rehli, M
Timblin, B
Tan, FL
Krause, SW
Skidgel, RA
机构
[1] Univ Illinois, Coll Med, Dept Pharmacol, Chicago, IL 60612 USA
[2] Univ Regensburg, Dept Hematol & Oncol, D-93042 Regensburg, Germany
[3] Univ Illinois, Coll Med, Dept Anesthesiol, Chicago, IL 60612 USA
关键词
metallocarboxypeptidase; genomic structure; transcription start site; THP-1; cells; initiator; downstream promoter element;
D O I
10.1016/S0378-1119(01)00898-8
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
The human carboxypeptidase M (CPM) gene was found to encompass similar to112.6 kb of genomic sequence, containing 11 exons of which eight (exons 2-9) are common to all transcripts and contain the entire coding region. We have cloned several alternative variants of CPM transcripts that result from differential promoter usage and alternative splicing. Although CPM belongs to the same metallocarboxypeptidase subfamily as CPE, their intron/exon structures differ significantly. Multiple transcription start sites were found in the CPM gene that cluster in two regions separated by similar to30 kb and are flanked by two unique functional promoters. One ('proximal') is immediately upstream of the coding region and contains GC-rich sequences and a typical TATA box whereas the other ('distal') consists almost entirely of repetitive elements. Luciferase reporter assays with constructs of the promoter regions showed they were both quite active in several cell lines. However, the proximal promoter was much stronger than the distal one in two of the human cell lines tested (HepG2 and HEK293) whereas both promoters were highly and equally active in the human monocytic cell line THP-1, which has high constitutive expression of CPM, (C) 2002 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:189 / 202
页数:14
相关论文
共 35 条
  • [1] ANDREESEN R, 1986, BLOOD, V67, P1257
  • [2] ANDREESEN R, 1988, CELL TISSUE RES, V253, P271
  • [3] Type 2 diabetes locus on 12q15 - Further mapping and mutation screening of two candidate genes
    Bektas, A
    Hughes, JN
    Warram, JH
    Krolewski, AS
    Doria, A
    [J]. DIABETES, 2001, 50 (01) : 204 - 208
  • [4] Characterization of the gene encoding human TAFI (thrombin-activable fibrinolysis inhibitor; plasma procarboxypeptidase B)
    Boffa, MB
    Reid, TS
    Joo, E
    Nesheim, ME
    Koschinsky, ML
    [J]. BIOCHEMISTRY, 1999, 38 (20) : 6547 - 6558
  • [5] RNAs from all categories generate retrosequences that may be exapted as novel genes or regulatory elements
    Brosius, J
    [J]. GENE, 1999, 238 (01) : 115 - 134
  • [6] The downstream core promoter element, DPE, is conserved from Drosophila to humans and is recognized by TAF(II)60 of Drosophila
    Burke, TW
    Kadonaga, JT
    [J]. GENES & DEVELOPMENT, 1997, 11 (22) : 3020 - 3031
  • [7] CHEN HM, 1993, J BIOL CHEM, V268, P8230
  • [8] DESAINTVIS B, 1995, BLOOD, V86, P1098
  • [9] Murine macrophage mannose receptor promoter is regulated by the transcription factors PU.1 and SP1
    Eichbaum, Q
    Heney, D
    Raveh, D
    Chung, M
    Davidson, M
    Epstein, J
    Ezekowitz, RAB
    [J]. BLOOD, 1997, 90 (10) : 4135 - 4143
  • [10] RESTRICTION OF INTERFERON-GAMMA RESPONSIVENESS AND BASAL EXPRESSION OF THE MYELOID HUMAN FC-GAMMA-R1B GENE IS MEDIATED BY A FUNCTIONAL PU.1 SITE AND A TRANSCRIPTION INITIATOR CONSENSUS
    EICHBAUM, QG
    IYER, R
    RAVEH, DP
    MATHIEU, C
    EZEKOWITZ, RAB
    [J]. JOURNAL OF EXPERIMENTAL MEDICINE, 1994, 179 (06) : 1985 - 1996