Growth hormone suppression of insulin-like growth factor binding protein-1 promoter activity

被引:9
作者
Lu, XP
Shi, ZD
Murphy, LJ [1 ]
机构
[1] Univ Manitoba, Dept Physiol, Winnipeg, MB R3E 0W3, Canada
[2] Univ Manitoba, Dept Internal Med, Winnipeg, MB R3E 0W3, Canada
基金
英国医学研究理事会;
关键词
AP-1; complexes; rat hepatocytes; DNase-1; footprinting; growth hormone;
D O I
10.1016/S0303-7207(99)00007-6
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Hepatic transcription of insulin-like growth factor binding protein-1 (IGFBP-1) is rapidly downregulated by growth hormone (GH) which is also known to induce expression of c-fos and c-jun. Go-expression of c-fos or c-jun in rat hepatocytes, individually or together, suppresses IGFBP-1 promoter activity by approximate to 60%. When hepatic nuclear extracts from sham-operated, hypophysectomized (hypox) and GH-treated hyper rats were analyzed by DNase-l footprinting, differences in the protection pattern were identified in three regions of the IGFBP-1 promoter. F1 corresponding to - 660 to - 640 bp showed acute changes in response to GH administration. In additional regions, F2 and F3, representing - 758 to - 748 bp and - 477 to - 447 bp; respectively, differences were apparent between nuclear extracts from the hyper and sham-operated rats. When F1 and F2 were removed by deletion of the region from - 824 to - 557 bp, the GH response was lost but suppression by co-expression of c-fos and c-jun was preserved. A putative AP-1 binding site was present in the F3 footprint region, however removal of F3 did not affect the GH responsiveness. These data indicate that several distinct sequences, other than the putative AP-1 site are involved in mediating the GH effects on IGFBP-1 transcription. (C) 1999 Elsevier Science Ireland Ltd. All rights reserved.
引用
收藏
页码:19 / 28
页数:10
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