A functional motif of long noncoding RNA Nron against osteoporosis

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作者
Fujun Jin
Junhui Li
Yong-Biao Zhang
Xiangning Liu
Mingxiang Cai
Meijing Liu
Mengyao Li
Cui Ma
Rui Yue
Yexuan Zhu
Renfa Lai
Zuolin Wang
Xunming Ji
Huawei Wei
Jun Dong
Zhiduo Liu
Yifei Wang
Yao Sun
Xiaogang Wang
机构
[1] The First Affiliated Hospital of Jinan University & Department of Stomatology,Clinical Research Platform for Interdiscipline of Stomatology
[2] College of stomatology,Beijing Advanced Innovation Center for Big Data
[3] Jinan University,Based Precision Medicine, School of Engineering Medicine
[4] Beihang University,Department of Oral Implantology, School of Stomatology
[5] Tongji University,Guangzhou Jinan Biomedicine Research and Development Center, National Engineering Research Center of Genetic Medicine, Institute of Biomedicine, College of Life Science and Technology
[6] Shanghai Engineering Research Center of Tooth Restoration and Regeneration,Shanghai Institute of Immunology, Department of Immunology and Microbiology
[7] Jinan University,Institute for Regenerative Medicine, Shanghai East Hospital, Frontier Science Center for Stem Cell Research, Shanghai Key Laboratory of Signaling and Disease Research, School of Life Sciences and Technology
[8] Shanghai Jiao Tong University School of Medicine,Department of Neurosurgery & China
[9] Tongji University,America Institute of Neuroscience
[10] Xuanwu Hospital,undefined
[11] Capital Medical University,undefined
[12] Zeki Biotechnology & Pharmaceutical Co. Ltd,undefined
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摘要
Long noncoding RNAs are widely implicated in diverse disease processes. Nonetheless, their regulatory roles in bone resorption are undefined. Here, we identify lncRNA Nron as a critical suppressor of bone resorption. We demonstrate that osteoclastic Nron knockout mice exhibit an osteopenia phenotype with elevated bone resorption activity. Conversely, osteoclastic Nron transgenic mice exhibit lower bone resorption and higher bone mass. Furthermore, the pharmacological overexpression of Nron inhibits bone resorption, while caused apparent side effects in mice. To minimize the side effects, we further identify a functional motif of Nron. The delivery of Nron functional motif to osteoclasts effectively reverses bone loss without obvious side effects. Mechanistically, the functional motif of Nron interacts with E3 ubiquitin ligase CUL4B to regulate ERα stability. These results indicate that Nron is a key bone resorption suppressor, and the lncRNA functional motif could potentially be utilized to treat diseases with less risk of side effects.
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