Gene expression and activity of enzymes in the arginine biosynthetic pathway in porcine fetal small intestine

被引:24
作者
Dekaney, CM [1 ]
Wu, GY [1 ]
Jaeger, LA [1 ]
机构
[1] Coll Vet Med, College Stn, TX 77843 USA
关键词
D O I
10.1203/01.PDR.0000047518.24941.76
中图分类号
R72 [儿科学];
学科分类号
100202 ;
摘要
We recently reported the presence of ornithine aminotransferase (OAT) enzymatic activity and mRNA expression in the intestine of fetal pigs from 30 to 110 d of gestation. Here we describe the activities and mRNA expression patterns of other key enzymes in the arginine biosynthetic pathway, specifically carbamoyl phosphate synthase I (CPS-I), ornithine carbamoyl transferase (OCT), and pyrroline-5-carboxylate reductase (P5CR), in the fetal porcine small intestine from 30 to 110 d of gestation. The activities of all three enzymes increased from d 30 to d 110 of gestation, and in situ hybridization demonstrates that 1) CPS-I and OCT genes are expressed in distinct patterns and are confined to the mucosal epithelium and 2) P5CR mRNA is present in mucosal epithelium and lamina propria of the fetal porcine small intestine from d 30 to d 110 of gestation. The presence of CPS-I and OCT in conjunction with the presence of OAT suggests that the fetal porcine small intestine is capable of synthesizing citrulline from P5C. In addition, the presence of P5CR suggests that the fetal porcine small intestine is able to synthesize proline from ornithine via OAT. This ability of the fetal small intestine to synthesize amino acids may be important for development and metabolic activity of the intestine during somatic gowth of the fetus.
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页码:274 / 280
页数:7
相关论文
共 32 条
[1]   PARTICIPATION OF ORNITHINE AMINOTRANSFERASE IN THE SYNTHESIS AND CATABOLISM OF ORNITHINE IN MICE - STUDIES USING GABACULINE AND ARGININE DEPRIVATION [J].
ALONSO, E ;
RUBIO, V .
BIOCHEMICAL JOURNAL, 1989, 259 (01) :131-138
[2]  
[Anonymous], [No title captured]
[3]   Intestinal brush-border membrane enzyme activities and transport functions during prenatal development of pigs [J].
Buddington, RK ;
Malo, C .
JOURNAL OF PEDIATRIC GASTROENTEROLOGY AND NUTRITION, 1996, 23 (01) :51-64
[4]   NG-hydroxy-L-arginine and nitric oxide inhibit Caco-2 tumor cell proliferation by distinct mechanisms [J].
Buga, GM ;
Wei, LH ;
Bauer, PM ;
Fukuto, JM ;
Ignarro, LJ .
AMERICAN JOURNAL OF PHYSIOLOGY-REGULATORY INTEGRATIVE AND COMPARATIVE PHYSIOLOGY, 1998, 275 (04) :R1256-R1264
[5]   Mucin gene expression in human embryonic and fetal intestine [J].
Buisine, MP ;
Devisme, L ;
Savidge, TC ;
Gespach, C ;
Gosselin, B ;
Porchet, N ;
Aubert, JP .
GUT, 1998, 43 (04) :519-524
[6]  
CARLSTEDT I, 1993, J BIOL CHEM, V268, P18771
[7]   Compartmentation and kinetics of urea cycle enzymes in porcine enterocytes [J].
Davis, PK ;
Wu, GY .
COMPARATIVE BIOCHEMISTRY AND PHYSIOLOGY B-BIOCHEMISTRY & MOLECULAR BIOLOGY, 1998, 119 (03) :527-537
[8]   Inhibition of laminin alpha 1-chain expression leads to alteration of basement membrane assembly and cell differentiation [J].
De Arcangelis, A ;
Neuville, P ;
Boukamel, R ;
Lefebvre, O ;
Kedinger, M ;
SimonAssmann, P .
JOURNAL OF CELL BIOLOGY, 1996, 133 (02) :417-430
[9]   Arginine-metabolizing enzymes in the developing rat small intestine [J].
De Jonge, WJ ;
Dingemanse, MA ;
De Boer, PAJ ;
Lamers, WH ;
Moorman, AFM .
PEDIATRIC RESEARCH, 1998, 43 (04) :442-451
[10]  
Dekaney CM, 1997, ANAT RECORD, V249, P517