DIFFERENTIAL REGULATION OF RAT T-KININOGEN BY TUMOR-NECROSIS-FACTOR AND INTERLEUKIN-6

被引:15
作者
ANDERSON, KP [1 ]
LINGREL, JB [1 ]
机构
[1] UNIV CINCINNATI,DEPT MOLEC GENET BIOCHEM & MICROBIOL,CINCINNATI,OH 45267
关键词
D O I
10.1210/mend-4-4-543
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Rat T-kininogen (T-KG), a cysteine protease inhibitor, is an acute phase reactant which is induced to high levels in response to inflammation. Both hormones and cytokines participate in this regulation. To investigate the cis-acting elements responsible for the induction of gene expression, various 5′-fragments of the rat T-KG gene were fused to a chloramphenicol acetyltransferase marker gene. These constructs were transfected into a rat hepatoma cell line which was then treated with tumor necrosis factor or interleukin-6 or both cytokines. Expression of the chloramphenicol acetyltransferase gene was induced with interleukin-6 treatment, but suppressed by tumor necrosis factor. The 5′-region of the T-KG gene responsible for conferring both of these effects was localized between nucleotides -404 to -210 upstream of the transcription start site. Fragments containing this region were found to be effective in either orientation, and could also regulate a heterologous promoter. © 1990 by The Endocrine Society.
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收藏
页码:543 / 550
页数:8
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