Molecular cloning and expression of rat kallistatin gene

被引:8
作者
Chai, KX
Chen, VC
Ni, AG
Lindpaintner, K
Rubattu, S
Chao, L
Chao, J
机构
[1] MED UNIV S CAROLINA,DEPT BIOCHEM & MOL BIOL,CHARLESTON,SC 29425
[2] HARVARD UNIV,CHILDRENS HOSP,SCH MED,BOSTON,MA 02115
[3] BRIGHAM & WOMENS HOSP,DEPT MED,DIV CARDIOVASC,BOSTON,MA 02115
[4] BRIGHAM & WOMENS HOSP,DEPT CARDIOL,BOSTON,MA 02115
来源
BIOCHIMICA ET BIOPHYSICA ACTA-GENE STRUCTURE AND EXPRESSION | 1997年 / 1353卷 / 03期
关键词
kallistatin; kallikrein-binding protein; serpin; gene cloning; promoter activity; recombinant protein; (rat);
D O I
10.1016/S0167-4781(97)00100-0
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
We have previously purified and cloned human kallistatin and rat kallikrein-binding protein (RKBP), which are tissue kallikrein inhibitors belonging to the serine proteinase inhibitor superfamily. In this study, we have cloned and sequenced the gene encoding rat kallistatin with Phe-Phe-Ser-Ala-Gln at positions P2-P3', which is identical to the reactive center of human kallistatin. Rat kallistatin is highly similar to human kallistatin, sharing 68% and 57% sequence identity at the cDNA and the amino acid levels. The rat kallistatin gene exists in a single copy and is located on chromosome 6. An SphI RFLP is found between SHR and WKY rats at or near the rat kallistatin gene locus. Two amino acid polymorphisms of the rat kallistatin gene between these two strains were found by sequence analysis. A candidate promoter in the 5'-flanking region (109 bp) of the rat kallistatin gene has been identified by reporter assays. The expression of rat kallistatin in the liver is growth-dependent and down-regulated during acute phase inflammation. Recombinant rat kallistatin produced in E. coli is able to bind to tissue kallikrein, and the interaction is inhibited by heparin. These characteristics define rat kallistatin as the counterpart of human kallistatin. (C) 1997 Elsevier Science B.V.
引用
收藏
页码:277 / 286
页数:10
相关论文
共 28 条
  • [1] BHOOLA KD, 1992, PHARMACOL REV, V44, P1
  • [2] THE SERPINS - EVOLUTION AND ADAPTATION IN A FAMILY OF PROTEASE INHIBITORS
    CARRELL, RW
    PEMBERTON, PA
    BOSWELL, DR
    [J]. COLD SPRING HARBOR SYMPOSIA ON QUANTITATIVE BIOLOGY, 1987, 52 : 527 - 535
  • [3] SUBSTRATE SPECIFICITIES OF TISSUE KALLIKREIN AND T-KININOGENASE - THEIR POSSIBLE ROLE IN KININOGEN PROCESSING
    CHAGAS, JR
    HIRATA, IY
    JULIANO, MA
    XIONG, W
    WANG, C
    CHAO, J
    JULIANO, L
    PRADO, ES
    [J]. BIOCHEMISTRY, 1992, 31 (21) : 4969 - 4974
  • [4] DETERMINANTS OF THE UNUSUAL CLEAVAGE SPECIFICITY OF LYSYL-BRADYKININ-RELEASING KALLIKREINS
    CHAGAS, JR
    PORTARO, FCV
    HIRATA, IY
    ALMEIDA, PC
    JULIANO, MA
    JULIANO, L
    PRADO, ES
    [J]. BIOCHEMICAL JOURNAL, 1995, 306 : 63 - 69
  • [5] CHAI KX, 1993, J BIOL CHEM, V268, P24498
  • [6] Genomic DNA sequence, expression, and chromosomal localization of the human B1 bradykinin receptor gene BDKRB1
    Chai, KX
    Ni, A
    Wang, DZ
    Ward, DC
    Chao, J
    Chao, L
    [J]. GENOMICS, 1996, 31 (01) : 51 - 57
  • [7] CHAI KX, 1991, J BIOL CHEM, V266, P16029
  • [8] MOLECULAR-CLONING, SEQUENCE-ANALYSIS, AND CHROMOSOMAL LOCALIZATION OF THE HUMAN PROTEASE INHIBITOR-4 (KALLISTATIN) GENE (PI4)
    CHAI, KX
    WARD, DC
    CHAO, J
    CHAO, L
    [J]. GENOMICS, 1994, 23 (02) : 370 - 378
  • [9] CHAO J, 1990, J BIOL CHEM, V265, P16394
  • [10] Chao J, 1992, Agents Actions Suppl, V38 ( Pt 1), P174