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类固醇生成急性调节蛋白(StAR)与胆固醇的线粒体内转运

Steroidogenic acute regulatory protein (StAR) and the intramitochondrial translocation of cholesterol.

作者信息

Christenson L K, Strauss J F

机构信息

Center for Research on Reproduction and Women's Health, University of Pennsylvania Medical Center, 1355 BRB II/III, 421 Curie Blvd, Philadelphia, PA 19104, USA.

出版信息

Biochim Biophys Acta. 2000 Dec 15;1529(1-3):175-87. doi: 10.1016/s1388-1981(00)00147-5.

Abstract

The steroidogenic acute regulatory (StAR) protein regulates the rate limiting step in steroidogenesis, the transport of cholesterol from the outer to the inner mitochondrial membrane. Insight into the structure and function of StAR was attained through molecular genetic studies of congenital lipoid adrenal hyperplasia, a rare disease caused by mutations in the StAR gene. Subsequent functional analysis defined two major domains within the StAR protein, the N-terminal mitochondrial targeting sequence and the C-terminus, which promotes the translocation of cholesterol between the two mitochondrial membranes. Two models of StAR's mechanism of action, (1) stimulation of cholesterol desorption from the outer mitochondrial membrane and (2) an intermembrane shuttle hypothesis, are discussed with respect to the known biochemical and biophysical events associated with the process of steroidogenesis and the structure of StAR. StAR gene expression is regulated primarily at the transcriptional level, and the roles of transcription factors that govern basal and cAMP-dependent StAR expression including SF-1, C/EBP beta, Sp1 and GATA-4 are reviewed.

摘要

类固醇生成急性调节(StAR)蛋白调节类固醇生成中的限速步骤,即胆固醇从线粒体外膜向内膜的转运。通过对先天性类脂性肾上腺增生症的分子遗传学研究,人们深入了解了StAR的结构和功能,该病是由StAR基因突变引起的一种罕见疾病。随后的功能分析确定了StAR蛋白内的两个主要结构域,即N端线粒体靶向序列和C端,后者促进胆固醇在线粒体内外膜之间的转运。结合与类固醇生成过程相关的已知生化和生物物理事件以及StAR的结构,讨论了StAR作用机制的两种模型:(1)刺激胆固醇从线粒体外膜解吸;(2)膜间穿梭假说。StAR基因表达主要在转录水平受到调控,本文综述了包括SF-1、C/EBPβ、Sp1和GATA-4在内的调控基础和cAMP依赖性StAR表达的转录因子的作用。

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