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基质金属蛋白酶及其组织抑制剂的转录调控

Transcriptional control of matrix metalloproteinases and the tissue inhibitors of matrix metalloproteinases.

作者信息

Borden P, Heller R A

机构信息

Institute of Biochemistry and Cell Biology, Syntex Discovery Research, Palo Alto, CA 94304, USA.

出版信息

Crit Rev Eukaryot Gene Expr. 1997;7(1-2):159-78. doi: 10.1615/critreveukargeneexpr.v7.i1-2.90.

Abstract

Matrix metalloproteinases (MMPs) are enzymes with important roles in a variety of normal physiological processes; these same enzymes are also operative in a range of pathologies. The proteins known as the tissue inhibitors of matrix metalloproteinases (TIMPs) act to limit the enzymatic function of the MMPs. MMPs and TIMPs can be divided into two groups with respect to gene expression: the majority exhibit inducible expression and a small number are produced constitutively or are expressed at very low levels and are not inducible. Among the agents that induce MMP and TIMP production are the inflammatory cytokines TNF alpha and IL1 beta. A marked cell type specificity is a hallmark of both MMP and TIMP gene expression (i.e., a limited number of cell types can be induced to make these proteins). An analysis of the control elements in the promoter regions of these proteins reveals a correlation between the presence of both AP-1 and Ets binding sites and inducible expression. The chromosomal locations of most of the MMPs and TIMPs have been verified; these data will provide the basis for investigations into possible correlations between mutations in these genes and disease states.

摘要

基质金属蛋白酶(MMPs)是在多种正常生理过程中发挥重要作用的酶;这些酶同样也在一系列病理过程中起作用。被称为基质金属蛋白酶组织抑制剂(TIMPs)的蛋白质可限制MMPs的酶功能。就基因表达而言,MMPs和TIMPs可分为两组:大多数表现为诱导性表达,少数组成性产生或表达水平极低且不可诱导。诱导MMP和TIMP产生的因子包括炎性细胞因子肿瘤坏死因子α和白细胞介素1β。显著的细胞类型特异性是MMP和TIMP基因表达的一个标志(即只有有限数量的细胞类型可被诱导产生这些蛋白质)。对这些蛋白质启动子区域调控元件的分析揭示了AP-1和Ets结合位点的存在与诱导性表达之间的相关性。大多数MMPs和TIMPs的染色体定位已得到证实;这些数据将为研究这些基因的突变与疾病状态之间可能的相关性提供基础。

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