Identification of a growth hormone-responsive STAT5-binding element in the rat insulin 1 gene

被引:80
作者
Galsgaard, ED
Gouilleux, F
Groner, B
Serup, P
Nielsen, JH
Billestrup, N
机构
[1] HAGEDORN RES LAB, DK-2820 GENTOFTE, DENMARK
[2] TUMOR BIOL CTR, INST EXPTL CANC RES, D-79106 FREIBURG, GERMANY
关键词
D O I
10.1210/me.10.6.652
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
GH and PRL stimulate both proliferation and insulin production in pancreatic beta-cells as well as in the rat insulinoma cell line RIN-5AH. We report here that human GH increases insulin mRNA levels in FIN-5AN cells via both somatogenic and lactogenic receptors. GH stimulated the rat insulin 1 promoter activity 2-fold, and this stimulation was abolished by introduction of a block mutation in a gamma-interferon-activated sequence (GAS)-like element (GLE) with the sequence 5'-TTCTGGGAA-3' located in the rat insulin 1 enhancer at position -330 to -322. This element, termed Ins-GLE, was able to confer GH responsiveness to a heterologous promoter. GH induced the binding of two protein complexes to the Ins-GLE. An antibody directed against the transcription factor STAT5 (signal transducer and activator of transcription) supershifted the GH-induced complexes. Furthermore, in COS7 cells transiently transfected with STAT5 and GH receptor cDNAs, it was found that expression of STAT5 was necessary for GH induction of these two DNA-binding complexes. These results suggest that GH stimulates insulin 1 promoter activity by inducing the binding of STAT5 to Ins-GLE.
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页码:652 / 660
页数:9
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