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视黄酸苯甲酸类化合物与核视黄酸受体

Retinobenzoic acids and nuclear retinoic acid receptors.

作者信息

Hashimoto Y

机构信息

Institute of Applied Microbiology, University of Tokyo, Japan.

出版信息

Cell Struct Funct. 1991 Apr;16(2):113-23. doi: 10.1247/csf.16.113.

Abstract

Retinoids (retinoic acid and its analogs) are widely involved in the control of cell proliferation, cell differentiation and embryonic development. A series of potent and novel synthetic retinoids named retinobenzoic acids has been developed. Retinobenzoic acids have proven to be useful tools in the investigation of the molecular mechanisms of retinoidal actions. Retinoids elicit their biological effects by binding to and activating specific nuclear receptors for retinoids (RAR's) which belong to the steroid/thyroid nuclear receptor superfamily. Recent investigations concerning the structure and function of nuclear receptors, namely of RAR's, are reviewed. Three subtypes of RAR (RAR-alpha, RAR-beta and RAR-gamma) have been identified so far. Each RAR is considered to play particular roles in the retinoidal actions. The role of each RAR is discussed in relation to their features and to the structure-activity relationships of retinoids. RAR's act as retinoid-dependent transcription factors which bind to a specific site of the gene and control its expression. Recent progress in the investigation of the interaction of RAR's with the responsive genes and with nuclear co-factors is reviewed. The diversity of retinoidal actions are possibly explained by the diversity of RAR's in their structure and in their spatial and temporal distribution, by the diversity of base sequences which interact with RAR's, by the diversity of cell type-specifically determined hierarchy of gene expression, and by the diversity of the nuclear factors which interact with RAR's.

摘要

类视黄醇(视黄酸及其类似物)广泛参与细胞增殖、细胞分化和胚胎发育的调控。一系列名为视黄基苯甲酸的强效新型合成类视黄醇已被开发出来。视黄基苯甲酸已被证明是研究类视黄醇作用分子机制的有用工具。类视黄醇通过与属于类固醇/甲状腺核受体超家族的类视黄醇特异性核受体(RAR)结合并激活它们来发挥其生物学效应。本文综述了关于核受体,即RAR的结构和功能的最新研究。到目前为止,已鉴定出三种RAR亚型(RAR-α、RAR-β和RAR-γ)。每种RAR被认为在类视黄醇作用中发挥特定作用。结合它们的特点以及类视黄醇的构效关系讨论了每种RAR的作用。RAR作为类视黄醇依赖性转录因子,与基因的特定位点结合并控制其表达。本文综述了RAR与反应基因以及核辅助因子相互作用研究的最新进展。类视黄醇作用的多样性可能由RAR在结构、空间和时间分布上的多样性、与RAR相互作用的碱基序列的多样性、细胞类型特异性决定的基因表达层次的多样性以及与RAR相互作用的核因子的多样性来解释。

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