<HashMap><database>biostudies-literature</database><scores><citationCount>0</citationCount><reanalysisCount>0</reanalysisCount><viewCount>70</viewCount><searchCount>0</searchCount></scores><additional><omics_type>Unknown</omics_type><volume>286(14)</volume><submitter>Hu R</submitter><pubmed_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.</pubmed_abstract><journal>The Journal of biological chemistry</journal><pagination>12328-39</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC3069436</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>A Runx2/miR-3960/miR-2861 regulatory feedback loop during mouse osteoblast differentiation.</pubmed_title><pmcid>PMC3069436</pmcid><pubmed_authors>Li H</pubmed_authors><pubmed_authors>Xia ZY</pubmed_authors><pubmed_authors>Zhou HD</pubmed_authors><pubmed_authors>Yang L</pubmed_authors><pubmed_authors>Xie H</pubmed_authors><pubmed_authors>Wu XP</pubmed_authors><pubmed_authors>Guo LJ</pubmed_authors><pubmed_authors>Chen C</pubmed_authors><pubmed_authors>Hu R</pubmed_authors><pubmed_authors>Luo XH</pubmed_authors><pubmed_authors>Liu W</pubmed_authors><view_count>70</view_count></additional><is_claimable>false</is_claimable><name>A Runx2/miR-3960/miR-2861 regulatory feedback loop during mouse osteoblast differentiation.</name><description>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.</description><dates><release>2011-01-01T00:00:00Z</release><publication>2011 Apr</publication><modification>2020-11-19T10:20:45Z</modification><creation>2019-06-05T16:23:40Z</creation></dates><accession>S-EPMC3069436</accession><cross_references><pubmed>21324897</pubmed><doi>10.1074/jbc.m110.176099</doi><doi>10.1074/jbc.M110.176099</doi></cross_references></HashMap>