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三碘甲状腺原氨酸抑制人生长激素启动子的转录。

Triiodothyronine inhibits transcription from the human growth hormone promoter.

作者信息

Morin A, Louette J, Voz M L, Tixier-Vidal A, Belayew A, Martial J A

机构信息

UAO 41115 CNRS, Laboratoire de Neuroendocrinologie Cellulaire, Collège de France, Paris.

出版信息

Mol Cell Endocrinol. 1990 Jul 9;71(3):261-7. doi: 10.1016/0303-7207(90)90031-3.

Abstract

Three DNA constructs, the natural human growth hormone gene (hGH-hGH) its 500 bp promoter linked to the chloramphenicol acetyl transferase reporter gene (hGH-CAT), and its structural part linked to the herpes virus thymidine kinase promoter (TK-hGH) were introduced into rat pituitary GC cells by DEAE-dextran transfection. Transient expression was followed as a function of triiodothyronine (T3) concentration. The hGH-CAT expression was specifically inhibited by T3 following a typical dose-response curve while hGH-GH gene expression was not significantly modified. The transient expression of TK-hGH increased as a function of T3 concentration. These results indicate that T3 exerts two opposite effects on hGH gene expression. First, it down-regulates expression by acting on the promoter; second, it up-regulates expression by acting on the structural part of the gene. These action could be due to regulation of transcription and mRNA stabilization, respectively.

摘要

通过DEAE-葡聚糖转染将三种DNA构建体导入大鼠垂体GC细胞,这三种构建体分别是天然人类生长激素基因(hGH-hGH)、其与氯霉素乙酰转移酶报告基因相连的500bp启动子(hGH-CAT)以及其与疱疹病毒胸苷激酶启动子相连的结构部分(TK-hGH)。以三碘甲状腺原氨酸(T3)浓度为函数跟踪瞬时表达情况。hGH-CAT表达受到T3的特异性抑制,呈现典型的剂量反应曲线,而hGH-GH基因表达没有明显改变。TK-hGH的瞬时表达随T3浓度升高而增加。这些结果表明,T3对hGH基因表达发挥两种相反的作用。首先,它通过作用于启动子下调表达;其次,它通过作用于基因的结构部分上调表达。这些作用可能分别归因于转录调控和mRNA稳定性调控。

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