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Thyrotropin-releasing hormone-stimulated thyrotropin expression involves islet-brain-1/c-Jun N-terminal kinase interacting protein-1.

作者信息

Abe Hiroshi, Murao Koji, Imachi Hitomi, Cao Wen M, Yu Xiao, Yoshida Kazuya, Wong Norman C W, Shupnik Margaret A, Haefliger Jacques-Antoine, Waeber Gérard, Ishida Toshihiko

机构信息

First Department of Internal Medicine, Faculty of Medicine, Kagawa University, Kagawa 761-0793, Japan.

出版信息

Endocrinology. 2004 Dec;145(12):5623-8. doi: 10.1210/en.2004-0635. Epub 2004 Sep 2.

Abstract

Islet-brain-1 (IB1)/c-Jun N-terminal kinase interacting protein 1 (JIP-1) is a scaffold protein that is expressed at high levels in neurons and the endocrine pancreas. IB1/JIP-1 interacts with the c-Jun N-terminal kinase and mediates the specific physiological stimuli (such as cytokines). However, the potential role of the protein in the pituitary has not been evaluated. Herein, we examined expression of the gene encoding IB1/JIP-1 and its translated product in the anterior pituitary gland and a pituitary cell line, GH3. We then examined the potential role of IB1/JIP-1 in controlling TSH-beta gene expression. Exposure of GH3 cells to TRH stimulated the expression of IB1/JIP-1 protein levels, mRNA, and transcription of the promoter. The increase of IB1/JIP-1 content by transient transfection study of a vector encoding IB1/JIP-1 or by the stimulation of TRH stimulates TSH-beta promoter activity. This effect is not found in the presence of a mutated nonfunctional (IB1S59N) IB1/JIP-1 protein. Together, these facts point to a central role of the IB1/JIP-1 protein in the control of TRH-mediated TSH-beta stimulation.

摘要

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