Promoter activity of carbonic anhydrase II regulatory regions in cultured renal proximal, tubular cells

被引:10
作者
Lai, LW
Erickson, RP
Venta, PJ
Tashian, RE
Lien, YHH
机构
[1] Univ Arizona, Hlth Sci Ctr, Dept Med, Nephrol Sect, Tucson, AZ 85724 USA
[2] Univ Arizona, Hlth Sci Ctr, Dept Pediat, Tucson, AZ 85724 USA
[3] Michigan State Univ, Dept Small Anim Clin Sci, E Lansing, MI 48224 USA
[4] Univ Michigan, Sch Med, Dept Human Genet, Ann Arbor, MI 48109 USA
关键词
carbonic anhydrase; promoter activity; renal cells;
D O I
10.1016/S0024-3205(98)00247-1
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Carbonic anhydrase II (CAII) plays an important role in the acid-base homeostasis of the body and its deficiency results in renal tubular acidosis. In order to identify the regulatory regions in the CATI gene for the future development of kidney-targeted gene therapy, we investigated the 5' region of the gene for its promoter activity. Deletion constructs with various lengths of the 5' flanking region of the human CAII promoter were ligated to the CAT reporter gene and lipofected in primary cultures of mouse proximal renal tubular cells and in cells of the established porcine proximal tubular cell line, LLC-PK1. The CAT activity was measured 48 hours after gene transfection. The -12000/CAT and -1300/CAT constructs expressed the highest CAT activity in both types of renal tubular cells (143- and 180-fold increase, respectively, in mouse proximal tubular cells; 50- and 70-fold increase, respectively, in LLC-PK, cells) but not the -420/CAT, -270/CAT, or -180/CAT constructs (9, 12, and 9% of that of -1300/CAT construct, respectively, in mouse proximal tubular cells and, 23, 9, and 8%, respectively, in LLC-PK1 cells, all p < 0.01 vs. -1300/CAT construct). No cytotoxicity was detected in the transfected cells. A computer search identified multiple putative transcription factor binding elements including Ap1 and Ap2 binding elements, which are present in the -1300/CAT construct but not in the shorter constructs. In conclusion, we demonstrate that the human CAII 5' sequence of proximal 1.3 kb contains strong promoter sequence(s) for renal tubular cells.
引用
收藏
页码:121 / 126
页数:6
相关论文
共 21 条
[1]   Depletion of intercalated cells from collecting ducts of carbonic anhydrase II-deficient (CAR2 null) mice [J].
Breton, S ;
Alper, SL ;
Gluck, SL ;
Sly, WS ;
Barker, JE ;
Brown, D .
AMERICAN JOURNAL OF PHYSIOLOGY-RENAL FLUID AND ELECTROLYTE PHYSIOLOGY, 1995, 269 (06) :F761-F774
[2]   FOS AND JUN - THE AP-1 CONNECTION [J].
CURRAN, T ;
FRANZA, BR .
CELL, 1988, 55 (03) :395-397
[3]  
Davenport HW, 1941, P SOC EXP BIOL MED, V48, P53
[4]   VARIATION IN ENZYMATIC TRANSIENT GENE-EXPRESSION ASSAYS [J].
HOLLON, T ;
YOSHIMURA, FK .
ANALYTICAL BIOCHEMISTRY, 1989, 182 (02) :411-418
[5]  
HULL RN, 1976, IN VITRO CELL DEV B, V12, P670, DOI 10.1007/BF02797469
[6]   PREPROENKEPHALIN PROMOTER YIELDS REGION-SPECIFIC AND LONG-TERM EXPRESSION IN ADULT BRAIN AFTER DIRECT IN-VIVO GENE-TRANSFER VIA A DEFECTIVE HERPES-SIMPLEX VIRAL VECTOR [J].
KAPLITT, MG ;
KWONG, AD ;
KLEOPOULOS, SP ;
MOBBS, CV ;
RABKIN, SD ;
PFAFF, DW .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1994, 91 (19) :8979-8983
[7]   HEPATIC GENE-THERAPY - PERSISTENT EXPRESSION OF HUMAN ALPHA-1-ANTITRYPSIN IN MICE AFTER DIRECT GENE DELIVERY INVIVO [J].
KAY, MA ;
LI, QT ;
LIU, TJ ;
LELAND, F ;
TOMAN, C ;
FINEGOLD, M ;
WOO, SLC .
HUMAN GENE THERAPY, 1992, 3 (06) :641-647
[8]   Kidney-targeted liposome-mediated gene transfer in mice [J].
Lai, LW ;
Moeckel, GW ;
Lien, YHH .
GENE THERAPY, 1997, 4 (05) :426-431
[9]   N-ETHYL-N-NITROSOUREA INDUCED NULL MUTATION AT THE MOUSE CAR-2 LOCUS - AN ANIMAL-MODEL FOR HUMAN CARBONIC ANHYDRASE-II DEFICIENCY SYNDROME [J].
LEWIS, SE ;
ERICKSON, RP ;
BARNETT, LB ;
VENTA, PJ ;
TASHIAN, RE .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1988, 85 (06) :1962-1966
[10]  
LIEN YH, 1997, KIDNEY INT S61, V52, pS85