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大鼠胰岛素1基因中生长激素反应性STAT5结合元件的鉴定。

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

作者信息

Galsgaard E D, Gouilleux F, Groner B, Serup P, Nielsen J H, Billestrup N

机构信息

Hagedom Research Institute, Gentofte, Denmark.

出版信息

Mol Endocrinol. 1996 Jun;10(6):652-60. doi: 10.1210/mend.10.6.8776725.

Abstract

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.

摘要

生长激素(GH)和催乳素(PRL)可刺激胰腺β细胞以及大鼠胰岛素瘤细胞系RIN - 5AH的增殖和胰岛素生成。我们在此报告,人GH通过生长激素受体和催乳素受体增加RIN - 5AH细胞中胰岛素mRNA水平。GH刺激大鼠胰岛素1启动子活性增加2倍,并且通过在位于大鼠胰岛素1增强子-330至-322位置、序列为5'-TTCTGGGAA-3'的γ-干扰素激活序列(GAS)样元件(GLE)中引入阻断突变,这种刺激作用被消除。这个元件,称为Ins - GLE,能够赋予异源启动子对GH的反应性。GH诱导两种蛋白质复合物与Ins - GLE结合。一种针对转录因子信号转导子和转录激活子5(STAT5)的抗体使GH诱导的复合物发生超迁移。此外,在瞬时转染了STAT5和GH受体cDNA的COS7细胞中,发现STAT5的表达对于GH诱导这两种DNA结合复合物是必需的。这些结果表明,GH通过诱导STAT5与Ins - GLE结合来刺激胰岛素1启动子活性。

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