Comparative analysis of the ontogeny of a sodium-dependent bile acid transporter in rat kidney and ileum

被引:83
作者
Christie, DM
Dawson, PA
Thevananther, S
Schneider, BL
机构
[1] YALE UNIV, DEPT PEDIAT, SCH MED, DIV PEDIAT GASTROENTEROL HEPATOL, NEW HAVEN, CT 06520 USA
[2] WAKE FOREST UNIV, BOWMAN GRAY SCH MED, DEPT INTERNAL MED GASTROENTEROL, WINSTON SALEM, NC 27157 USA
来源
AMERICAN JOURNAL OF PHYSIOLOGY-GASTROINTESTINAL AND LIVER PHYSIOLOGY | 1996年 / 271卷 / 02期
关键词
apical; development; membrane protein; nuclear run-on; transport; messenger ribonucleic acid stability;
D O I
10.1152/ajpgi.1996.271.2.G377
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
An apical sodium-dependent bile acid transporter (ASBT) has recently been cloned and characterized in the rat ileum. Northern and Western blotting revealed both the ASBT mRNA and protein in rat kidney. The coding sequence of the kidney transcript was found to be identical to the previously cloned ileal ASBT. Indirect immunofluorescence studies localized the ASBT protein to the apical membrane of the renal proximal convoluted tubule. Kinetic analysis of sodium-dependent taurocholate uptake using membrane vesicles revealed a similar Michaelis-Menten constant value for taurocholate in the kidney and intestine. ASBT protein and function were present in the kidney but not the ileum from 7-day-old rats. On postnatal day 7, there was a sevenfold increase in ASBT steady-state mRNA levels in the kidney relative to the ileum, yet nuclear run-on assays revealed that the nascent transcription rates at this age were virtually the same. This suggests that the difference in the neonatal expression of the ASBT gene in the kidney and ileum may be in part due to differences in mRNA stability.
引用
收藏
页码:G377 / G385
页数:9
相关论文
共 30 条
[1]   ATP-DEPENDENT TAUROCHOLATE TRANSPORT BY RAT-LIVER CANALICULAR MEMBRANE-VESICLES [J].
ADACHI, Y ;
KOBAYASHI, H ;
KURUMI, Y ;
SHOUJI, M ;
KITANO, M ;
YAMAMOTO, T .
HEPATOLOGY, 1991, 14 (04) :655-659
[2]   ONTOGENESIS OF TAUROCHOLATE TRANSPORT BY RAT ILEAL BRUSH-BORDER MEMBRANE-VESICLES [J].
BARNARD, JA ;
GHISHAN, FK ;
WILSON, FA .
JOURNAL OF CLINICAL INVESTIGATION, 1985, 75 (03) :869-873
[3]  
Booth A G, 1974, Biochem J, V142, P575
[4]  
BRADFORD MM, 1976, ANAL BIOCHEM, V72, P248, DOI 10.1016/0003-2697(76)90527-3
[5]   SELECTIVE DEGRADATION OF EARLY-RESPONSE-GENE MESSENGER-RNAS - FUNCTIONAL ANALYSES OF SEQUENCE FEATURES OF THE AU-RICH ELEMENTS [J].
CHEN, CYA ;
SHYU, AB .
MOLECULAR AND CELLULAR BIOLOGY, 1994, 14 (12) :8471-8482
[6]   ISOLATION OF BIOLOGICALLY-ACTIVE RIBONUCLEIC-ACID FROM SOURCES ENRICHED IN RIBONUCLEASE [J].
CHIRGWIN, JM ;
PRZYBYLA, AE ;
MACDONALD, RJ ;
RUTTER, WJ .
BIOCHEMISTRY, 1979, 18 (24) :5294-5299
[7]  
CONNELL C, 1987, BIOTECHNIQUES, V5, P342
[8]  
DARNELL JE, 1982, NATURE, V297, P283
[9]   MECHANISMS OF MESSENGER-RNA DEGRADATION IN EUKARYOTES [J].
DECKER, CJ ;
PARKER, R .
TRENDS IN BIOCHEMICAL SCIENCES, 1994, 19 (08) :336-340
[10]   REGULATION OF GROWTH-HORMONE MESSENGER-RNA SYNTHESIS BY DEXAMETHASONE AND TRIIODOTHYRONINE - TRANSCRIPTIONAL RATE AND MESSENGER-RNA STABILITY CHANGES IN PITUITARY-TUMOR CELLS [J].
DIAMOND, DJ ;
GOODMAN, HM .
JOURNAL OF MOLECULAR BIOLOGY, 1985, 181 (01) :41-62