Involvement of nuclear factor-I (NF1) binding motif in the regucalcin gene expression of rat kidney cortex: The expression is suppressed by cisplatin administration

被引:15
作者
Misawa, H [1 ]
Yamaguchi, M [1 ]
机构
[1] Univ Shizuoka, Grad Sch Nutr Sci, Lab Endocrinol & Mol Metab, Shizuoka 4228526, Japan
关键词
regucalcin; nuclear factor 1 (NF1); gene expression; cisplatin; rat kidney;
D O I
10.1023/A:1011040805597
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
The binding of nuclear factor on the promoter region of the regucalcin gene and the expression of regucalcin in the kidney cortex of rats was investigated. Nuclear extracts from kidney cortex were used for oligonucleotide competition gel mobility shift assay. An oligonucleotide between position -523 and -506 in the 5'-flanking region of the rat regucalcin gene, which contains a nuclear factor I (NF1) consensus motif TTGGC(N)(6)CC, competed with the probe for the binding of the nuclear protein from kidney cortex. The mutation of TTGGC in the consensus sequence caused an inhibition of the binding of nuclear factors. The binding of nuclear factor on the 5'-flanking region was clearly reduced in the kidney cortex obtained at 1, 2, and 3 days after a single intraperitoneal administration of cisplatin (1.0 mg/100 g body wt) to rats. Moreover, cisplatin administration caused a remarkable decrease in regucalcin mRNA levels and regucalcin concentration in the kidney cortex. Also, serum regucalcin concentration was significantly decreased by cisplatin administration. Meanwhile, serum urea nitrogen concentration was markedly elevated by cisplatin administration. The present study demonstrates that the specific nuclear factor binds to the NF1-like sequence in the promotor region of regucalcin gene in the kidney cortex of rats, and that the nuclear factor binding and regucalcin expression are suppressed by cisplatin administration.
引用
收藏
页码:29 / 37
页数:9
相关论文
共 38 条
[1]  
AGUS ZS, 1997, AM J PHYSIOL, V232, P545
[2]  
BRADFORD MM, 1976, ANAL BIOCHEM, V72, P248, DOI 10.1016/0003-2697(76)90527-3
[3]  
Cheung W. Y., 1984, SCIENCE, V202, P19
[4]   ACCURATE TRANSCRIPTION INITIATION BY RNA POLYMERASE-II IN A SOLUBLE EXTRACT FROM ISOLATED MAMMALIAN NUCLEI [J].
DIGNAM, JD ;
LEBOVITZ, RM ;
ROEDER, RG .
NUCLEIC ACIDS RESEARCH, 1983, 11 (05) :1475-1489
[6]   Expanding the TRANSFAC database towards an expert system of regulatory molecular mechanisms [J].
Heinemeyer, T ;
Chen, X ;
Karas, H ;
Kel, AE ;
Kel, OV ;
Liebich, I ;
Meinhardt, T ;
Reuter, I ;
Schacherer, F ;
Wingender, E .
NUCLEIC ACIDS RESEARCH, 1999, 27 (01) :318-322
[7]   INTRACELLULAR CALCIUM-BINDING PROTEINS - MORE SITES THAN INSIGHTS [J].
HEIZMANN, CW ;
HUNZIKER, W .
TRENDS IN BIOCHEMICAL SCIENCES, 1991, 16 (03) :98-103
[8]   The role of intracellular Ca2+ in the regulation of gluconeogenesis [J].
KrausFriedmann, N ;
Feng, L .
METABOLISM-CLINICAL AND EXPERIMENTAL, 1996, 45 (03) :389-403
[9]   Glial fibrillary acidic protein transcription responses to transforming growth factor-β1 and interleukin-1β are mediated by a nuclear factor-1-like site in the near-upstream promoter [J].
Krohn, K ;
Rozovsky, I ;
Wals, P ;
Teter, B ;
Anderson, CP ;
Finch, CE .
JOURNAL OF NEUROCHEMISTRY, 1999, 72 (04) :1353-1361
[10]   SUPPRESSED EXPRESSION OF CALCIUM-BINDING PROTEIN REGUCALCIN MESSENGER-RNA IN THE RENAL-CORTEX OF RATS WITH CHEMICALLY-INDUCED KIDNEY DAMAGE [J].
KUROTA, H ;
YAMAGUCHI, M .
MOLECULAR AND CELLULAR BIOCHEMISTRY, 1995, 151 (01) :55-60