Department of Medical Genetics, University of British Columbia, Centre for Molecular Medicine and Therapeutics, and Child & Family Research Institute, Vancouver, BC, Canada.
Mol Cell Endocrinol. 2011 Mar 1;334(1-2):49-55. doi: 10.1016/j.mce.2010.04.021. Epub 2010 May 10.
Nuclear hormone receptors (NHRs) are proteins that regulate gene expression in response to developmental, environmental, and nutritional signals. The activity of some NHRs is selectively and reversibly modulated by small molecular weight compounds. However, for others - termed "orphan" receptors - no such ligands have (yet) been identified, and at least some NHRs may lack natural ligands. NHRs exhibit a stereotyped architecture, with conserved N-terminal DNA-binding domains (DBDs) and more variable C-terminal ligand-binding domains (LBDs). NHRs control the transcription of remarkably diverse and specific gene networks, apparently by integrating multiple regulatory inputs that interact with distinct receptor surfaces; these inputs include small molecule ligands, transcriptional coregulators, and response elements, the genomic sites to which the receptors bind. NHRs comprise an ancient superfamily found in all metazoans, and recent findings have revealed NHR-like regulatory factors in fungi. Here, we consider NHR function and evolution in nematodes, roundworms that inhabit terrestrial, marine, and freshwater habitats; we focus in particular on the well-established experimental organism Caenorhabditis elegans. Interestingly, the C. elegans genome encodes a massively expanded NHR family; we speculate that some of the multiple physiological activities governed by individual mammalian NHRs may be distributed among multiple members of the C. elegans family, potentially focusing and simplifying functional analyses. Accordingly, investigations of relevant NHR cofactors, ligands, and response elements might also prove to be simpler; moreover, the abbreviated intergenic regions of the C. elegans genome will facilitate the assignment of response elements to target genes. Finally, the growing interest in medically relevant nematodes is providing novel insights into the function and evolution of NHRs.
核激素受体(NHRs)是一类蛋白质,它们能够响应发育、环境和营养信号来调节基因表达。一些 NHRs 的活性可以被小分子化合物选择性和可逆地调节。然而,对于其他被称为“孤儿”受体的 NHRs 来说,尚未发现其配体,而且至少一些 NHRs 可能缺乏天然配体。NHRs 具有一种典型的结构,包含保守的 N 端 DNA 结合结构域(DBDs)和更可变的 C 端配体结合结构域(LBDs)。NHRs 控制着多样性和特异性基因网络的转录,这显然是通过整合与不同受体表面相互作用的多种调节输入来实现的;这些输入包括小分子配体、转录共激活因子和反应元件,即受体结合的基因组位点。NHRs 构成了一个在所有后生动物中都存在的古老超家族,最近的研究结果揭示了真菌中存在 NHR 样调节因子。在这里,我们考虑了线虫(一种生活在陆地、海洋和淡水中的圆形蠕虫)中的 NHR 功能和进化;我们特别关注已经确立的实验生物秀丽隐杆线虫。有趣的是,秀丽隐杆线虫的基因组编码了一个大规模扩展的 NHR 家族;我们推测,一些由单个哺乳动物 NHRs 控制的多种生理活性可能分布在秀丽隐杆线虫家族的多个成员中,这可能会使功能分析更加集中和简化。因此,对相关 NHR 共因子、配体和反应元件的研究也可能会变得更加简单;此外,秀丽隐杆线虫基因组中较短的基因间区将有助于将反应元件分配给靶基因。最后,对具有医学相关性的线虫的日益关注,为 NHR 的功能和进化提供了新的见解。