Lee Yong-Soo, Chanda Dipanjan, Sim Jeonggu, Park Yun-Yong, Choi Hueng-Sik
Hormone Research Center, School of Biological Sciences and Technology, Chonnam National University, Gwangju 500-757, Korea.
Int Rev Cytol. 2007;261:117-58. doi: 10.1016/S0074-7696(07)61003-1.
The small heterodimer partner (SHP; NROB2) is a member of the nuclear receptor superfamily and is classified as an "orphan" subgroup, as its ligand has not yet been identified. SHP lacks the classical DNA-binding domain found in most nuclear receptors and functions as a transcriptional coregulator by directly interacting with nuclear receptors and other transcription factors. SHP regulates the transcription of a variety of target genes and controls a variety of physiological functions. For the past 10 years, great progress has been made in our understanding of the mechanism of action of SHP and the regulation of SHP gene expression. Many of the results imply that SHP has a variety of roles in the regulation of metabolic homeostasis. In this review, we discuss the current state of understanding of the structure, expression, and function of the orphan nuclear receptor, SHP.
小异二聚体伴侣蛋白(SHP;核受体辅抑制因子2)是核受体超家族的成员,由于其配体尚未确定,被归类为“孤儿”亚组。SHP缺乏大多数核受体中发现的经典DNA结合结构域,通过直接与核受体和其他转录因子相互作用而作为转录共调节因子发挥作用。SHP调节多种靶基因的转录并控制多种生理功能。在过去十年中,我们对SHP的作用机制和SHP基因表达调控的理解取得了很大进展。许多结果表明,SHP在代谢稳态调节中具有多种作用。在本综述中,我们讨论了对孤儿核受体SHP的结构、表达和功能的当前理解状态。