Laboratory of Endocrinology and Receptor Biology, NIDDK, National Institutes of Health, Bethesda, MD, United States.
Laboratory of Endocrinology and Receptor Biology, NIDDK, National Institutes of Health, Bethesda, MD, United States.
Curr Top Dev Biol. 2017;125:227-255. doi: 10.1016/bs.ctdb.2016.11.009. Epub 2016 Dec 27.
The ability to generate neuronal diversity is central to the function of the nervous system. Here we discuss the key neurodevelopmental roles of retinoid-related orphan receptor β (RORβ) encoded by the Rorb (Nr1f2) gene. Recent studies have reported loss of function of the human RORB gene in cases of familial epilepsy and intellectual disability. Principal sites of expression of the Rorb gene in model species include sensory organs, the spinal cord, and brain regions that process sensory and circadian information. Genetic analyses in mice have indicated functions in circadian behavior, vision, and, at the cellular level, the differentiation of specific neuronal cell types. Studies in the retina and sensory areas of the cerebral cortex suggest that this orphan nuclear receptor acts at decisive steps in transcriptional hierarchies that determine neuronal diversity.
产生神经元多样性的能力是神经系统功能的核心。在这里,我们讨论了由 Rorb(Nr1f2)基因编码的视黄酸相关孤儿受体 β(RORβ)的关键神经发育作用。最近的研究报告了人类 RORB 基因在家族性癫痫和智力残疾病例中的功能丧失。Rorb 基因在模型物种中的主要表达部位包括感觉器官、脊髓和处理感觉和昼夜节律信息的大脑区域。在小鼠中的遗传分析表明,其具有昼夜节律行为、视觉以及在细胞水平上分化特定神经元细胞类型的功能。在视网膜和大脑皮层的感觉区域的研究表明,这种孤儿核受体在决定神经元多样性的转录层次结构的决定性步骤中发挥作用。