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Runx2/miR-3960/miR-2861 调控反馈环路在小鼠成骨细胞分化过程中的作用。

A Runx2/miR-3960/miR-2861 regulatory feedback loop during mouse osteoblast differentiation.

机构信息

Institute of Endocrinology and Metabolism, The Second Xiangya Hospital of Central South University, 139 Middle Renmin Road, Changsha, Hunan 410011, China.

出版信息

J Biol Chem. 2011 Apr 8;286(14):12328-39. doi: 10.1074/jbc.M110.176099. Epub 2011 Feb 15.

Abstract

Our recent study showed that miR-2861 promotes osteoblast differentiation by targeting histone deacetylase 5, resulting in increased runt-related transcription factor 2 (Runx2) protein production. Here we identified another new microRNA (miRNA) (miR-3960) that played a regulatory role in osteoblast differentiation through a regulatory feedback loop with miR-2861. miR-3960 and miR-2861 were found clustered at the same loci. miR-3960 was transcribed during bone morphogenic protein 2 (BMP2)-induced osteogenesis of ST2 stromal cells. Overexpression of miR-3960 promoted BMP2-induced osteoblastogenesis. However, the inhibition of miR-3960 expression attenuated the osteoblastogenesis. Homeobox A2 (Hoxa2), a repressor of Runx2 expression, was confirmed to be a target of miR-3960. Electrophoretic mobility shift assay and chromatin immunoprecipitation experiments confirmed that Runx2 bound to the promoter of the miR-3960/miR-2861 cluster. Furthermore, overexpression of Runx2 induced miR-3960/miR-2861 transcription, and block of Runx2 expression attenuated BMP2-induced miR-3960/miR-2861 transcription. Here we report that miR-3960 and miR-2861, transcribed together from the same miRNA polycistron, both function in osteoblast differentiation through a novel Runx2/miR-3960/miR-2861 regulatory feedback loop. Our findings provide new insights into the roles of miRNAs in osteoblast differentiation.

摘要

我们最近的研究表明,miR-2861 通过靶向组蛋白去乙酰化酶 5 促进成骨细胞分化,导致 runt 相关转录因子 2(Runx2)蛋白产量增加。在这里,我们鉴定了另一种新的 microRNA(miRNA)(miR-3960),它通过与 miR-2861 的调节反馈环在成骨细胞分化中发挥调节作用。miR-3960 和 miR-2861 被发现位于同一基因座上。miR-3960 在骨形态发生蛋白 2(BMP2)诱导的 ST2 基质细胞成骨过程中被转录。miR-3960 的过表达促进了 BMP2 诱导的成骨作用。然而,miR-3960 表达的抑制减弱了成骨作用。Runx2 表达的抑制剂同源盒 A2(Hoxa2)被证实是 miR-3960 的靶标。电泳迁移率变动分析和染色质免疫沉淀实验证实 Runx2 结合到 miR-3960/miR-2861 簇的启动子上。此外,Runx2 的过表达诱导了 miR-3960/miR-2861 的转录,而 Runx2 表达的阻断减弱了 BMP2 诱导的 miR-3960/miR-2861 转录。在这里,我们报告说,miR-3960 和 miR-2861 从同一个 miRNA 多顺反子转录,它们都通过一个新的 Runx2/miR-3960/miR-2861 调节反馈环在成骨细胞分化中发挥作用。我们的发现为 miRNA 在成骨细胞分化中的作用提供了新的见解。

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