Sawatsubashi Shun, Nishimura Koichi, Mori Jinichi, Kouzmenko Alexander, Kato Shigeaki
Department of Molecular Endocrinology, Fujii Memorial Institute of Medical Sciences, Institute of Advanced Medical Sciences, Tokushima University, Tokushima, Japan.
Center for Regional Cooperation, Iwaki Meisei University, Iwaki, Japan.
J Bone Metab. 2019 Feb;26(1):3-12. doi: 10.11005/jbm.2019.26.1.3. Epub 2019 Feb 28.
Vitamin D (VD) is essential for bone health, and VD or its analogues are widely used in clinics to ameliorate bone loss. The targets and mode of VD anti-osteoporotic actions appear to be different from those of other classes of drugs modulating bone remodeling. VD exerts its biological activities through the nuclear VD receptor (VDR)-mediated transcriptional regulation of target mRNA and non-coding RNA genes. VD-induced gene regulation involves epigenetic modifications of chromatin conformation at the target loci as well as reconfiguration of higher-order chromosomal organization through VDR-mediated recruitment of various regulatory factors. Enhancer RNAs (eRNA), a class of non-coding enhancer-derived RNAs, have recently emerged as VDR target gene candidates that act through reorganization of chromatin looping to induce enhancer-promoter interaction in activation of mRNA-encoding genes. This review outlines the molecular mechanisms of VD actions mediated by the VDR and suggests novel function of eRNAs in VDR transactivation.
维生素D(VD)对骨骼健康至关重要,VD或其类似物在临床上被广泛用于改善骨质流失。VD抗骨质疏松作用的靶点和模式似乎与其他调节骨重塑的药物不同。VD通过核VD受体(VDR)介导的靶mRNA和非编码RNA基因的转录调控发挥其生物学活性。VD诱导的基因调控涉及靶位点染色质构象的表观遗传修饰,以及通过VDR介导的各种调控因子的募集对高阶染色体组织的重新配置。增强子RNA(eRNA)是一类非编码增强子衍生的RNA,最近已成为VDR靶基因候选物,其通过染色质环化的重组发挥作用,以诱导增强子-启动子相互作用来激活编码mRNA的基因。本综述概述了由VDR介导的VD作用的分子机制,并提出了eRNA在VDR反式激活中的新功能。