Key result
Growth hormone stimulated rat insulin 1 promoter activity 2-fold by inducing the binding of STAT5 to a gamma-interferon-activated sequence-like element (Ins-GLE).
Growth hormone stimulates insulin 1 promoter activity by inducing the binding of the transcription factor STAT5 to a specific element (Ins-GLE) in the rat insulin 1 gene.
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May link GH to insulin transcription via STAT5; leaves open relevance to human islets or glucose homeostasis.
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 RIN-5AH 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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Galsgaard et al. (1996) studied this question. Growth hormone (GH) was evaluated on Rat insulin 1 promoter activity (2-fold increase). Growth hormone stimulated rat insulin 1 promoter activity 2-fold by inducing the binding of STAT5 to a gamma-interferon-activated sequence-like element (Ins-GLE).
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