<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Smith SS</submitter><funding>UConn Health</funding><funding>NIDCR NIH HHS</funding><funding>National Institutes of Health</funding><funding>NIAMS NIH HHS</funding><funding>American Society for Bone and Mineral Research</funding><pagination>21717-21728</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC5076840</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>291(41)</volume><pubmed_abstract>Serum glucocorticoids play a critical role in synchronizing circadian rhythm in peripheral tissues, and multiple mechanisms regulate tissue sensitivity to glucocorticoids. In the skeleton, circadian rhythm helps coordinate bone formation and resorption. Circadian rhythm is regulated through transcriptional and post-transcriptional feedback loops that include microRNAs. How microRNAs regulate circadian rhythm in bone is unexplored. We show that in mouse calvaria, miR-433 displays robust circadian rhythm, peaking just after dark. In C3H/10T1/2 cells synchronized with a pulse of dexamethasone, inhibition of miR-433 using a tough decoy altered the period and amplitude of Per2 gene expression, suggesting that miR-433 regulates rhythm. Although miR-433 does not directly target the Per2 3'-UTR, i</pubmed_abstract><journal>The Journal of biological chemistry</journal><pubmed_title>MicroRNA-433 Dampens Glucocorticoid Receptor Signaling, Impacting Circadian Rhythm and Osteoblastic Gene Expression.</pubmed_title><pmcid>PMC5076840</pmcid><funding_grant_id>AR044877</funding_grant_id><funding_grant_id>5T90DE21989</funding_grant_id><funding_grant_id>R56 AR044877</funding_grant_id><funding_grant_id>R29 AR044877</funding_grant_id><funding_grant_id>T90 DE021989</funding_grant_id><funding_grant_id>R01 AR044877</funding_grant_id><funding_grant_id>Grant-In-Aid</funding_grant_id><pubmed_authors>Franceschetti T</pubmed_authors><pubmed_authors>Dole NS</pubmed_authors><pubmed_authors>Smith SS</pubmed_authors><pubmed_authors>Hrdlicka HC</pubmed_authors><pubmed_authors>Delany AM</pubmed_authors></additional><is_claimable>false</is_claimable><name>MicroRNA-433 Dampens Glucocorticoid Receptor Signaling, Impacting Circadian Rhythm and Osteoblastic Gene Expression.</name><description>Serum glucocorticoids play a critical role in synchronizing circadian rhythm in peripheral tissues, and multiple mechanisms regulate tissue sensitivity to glucocorticoids. In the skeleton, circadian rhythm helps coordinate bone formation and resorption. Circadian rhythm is regulated through transcriptional and post-transcriptional feedback loops that include microRNAs. How microRNAs regulate circadian rhythm in bone is unexplored. We show that in mouse calvaria, miR-433 displays robust circadian rhythm, peaking just after dark. In C3H/10T1/2 cells synchronized with a pulse of dexamethasone, inhibition of miR-433 using a tough decoy altered the period and amplitude of Per2 gene expression, suggesting that miR-433 regulates rhythm. Although miR-433 does not directly target the Per2 3'-UTR, i</description><dates><release>2016-01-01T00:00:00Z</release><publication>2016 Oct</publication><modification>2025-04-04T09:21:13.459Z</modification><creation>2019-03-27T02:27:23Z</creation></dates><accession>S-EPMC5076840</accession><cross_references><pubmed>27551048</pubmed><doi>10.1074/jbc.M116.737890</doi><doi>10.1074/jbc.m116.737890</doi></cross_references></HashMap>