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I型胶原蛋白基因调控与肝硬化的分子发病机制

Type I collagen gene regulation and the molecular pathogenesis of cirrhosis.

作者信息

Brenner D A, Westwick J, Breindl M

机构信息

Department of Medicine, University of California, La Jolla.

出版信息

Am J Physiol. 1993 Apr;264(4 Pt 1):G589-95. doi: 10.1152/ajpgi.1993.264.4.G589.

Abstract

Cirrhosis is characterized by an increased deposition of extracellular matrix proteins, including type I collagen. Type I collagen is a product of two genes, alpha 1(I) and alpha 2(I), which are generally coordinately regulated. Since expression of type I collagen genes is increased during cirrhosis, understanding the structure and function of the regulatory components of the type I collagen genes should provide insight into the molecular pathogenesis of cirrhosis. This review will analyze the collagen alpha 1(I) gene with respect to chromatin structure, DNA methylation, regulation by agonists, and DNA-protein interactions.

摘要

肝硬化的特征是细胞外基质蛋白沉积增加,包括I型胶原。I型胶原是由两个基因α1(I)和α2(I)产生的产物,这两个基因通常受到协同调控。由于I型胶原基因的表达在肝硬化期间增加,了解I型胶原基因调控成分的结构和功能应该有助于深入了解肝硬化的分子发病机制。本综述将从染色质结构、DNA甲基化、激动剂调控以及DNA-蛋白质相互作用等方面分析胶原α1(I)基因。

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