Regulation of the steroidogenic acute regulatory protein gene expression: present and future perspectives

被引:243
作者
Manna, Pulak R. [1 ]
Dyson, Matthew T. [1 ]
Stocco, Douglas M. [1 ]
机构
[1] Texas Tech Univ, Hlth Sci Ctr, Dept Biochem & Cell Biol, Lubbock, TX 79430 USA
基金
美国国家卫生研究院;
关键词
StAR gene expression; cAMP signaling; AKAP; transcription; translation; LEYDIG TUMOR-CELLS; CCAAT/ENHANCER-BINDING-PROTEIN; HORMONE-SENSITIVE LIPASE; MESSENGER-RIBONUCLEIC-ACID; GROWTH-FACTOR-I; FOLLICLE-STIMULATING-HORMONE; LIPOID ADRENAL-HYPERPLASIA; RECEPTOR CLASS-B; CYCLIC-AMP; LUTEINIZING-HORMONE;
D O I
10.1093/molehr/gap025
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
Steroid hormones are synthesized in the adrenal gland, gonads, placenta and brain and are critical for normal reproductive function and bodily homeostasis. The steroidogenic acute regulatory (StAR) protein regulates the rate-limiting step in steroid biosynthesis, i.e. the delivery of cholesterol from the outer to the inner mitochondrial membrane. The expression of the StAR protein is predominantly regulated by cAMP-dependent mechanisms in the adrenal and gonads. Whereas StAR plays an indispensable role in the regulation of steroid biosynthesis, a complete understanding of the regulation of its expression and function in steroidogenesis is not available. It has become clear that the regulation of StAR gene expression is a complex process that involves the interaction of a diversity of hormones and multiple signaling pathways that coordinate the cooperation and interaction of transcriptional machinery, as well as a number of post-transcriptional mechanisms that govern mRNA and protein expression. However, information is lacking on how the StAR gene is regulated in vivo such that it is expressed at appropriate times during development and is confined to the steroidogenic cells. Thus, it is not surprising that the precise mechanism involved in the regulation of StAR gene has not yet been established, which is the key to understanding the regulation of steroidogenesis in the context of both male and female development and function.
引用
收藏
页码:321 / 333
页数:13
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