<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Song C</submitter><funding>Special Fund of Xinyang Normal University</funding><funding>National Natural Science Foundation of China</funding><funding>Program of National Beef Cattle and Yak Industrial Technology System</funding><pagination>591-604</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC6140903</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>13(6)</volume><pubmed_abstract>Long noncoding RNAs (lncRNAs) are involved in the regulation of skeletal muscle development. In the present study, differentially expressed lncRNAs were identified from RNA-seq data derived from myoblasts and myotubes. We conducted studies to elucidate the function and molecular mechanism of action of Linc-smad7 during skeletal muscle development. Our findings show that Linc-smad7 is upregulated during the early phase of myoblasts differentiation. In in vitro studies, we showed that overexpression of Linc-smad7 promoted the arrest of myoblasts in G1 phase, inhibited DNA replication, and induced myoblast differentiation. Our in vivo studies suggest that Linc-smad7 stimulates skeletal muscle regeneration in cardiotoxin-induced muscle injury. Mechanistically, Linc-smad7 overexpression increas</pubmed_abstract><journal>Epigenetics</journal><pubmed_title>Linc-smad7 promotes myoblast differentiation and muscle regeneration via sponging miR-125b.</pubmed_title><pmcid>PMC6140903</pmcid><funding_grant_id>2017001</funding_grant_id><funding_grant_id>CARS-38</funding_grant_id><funding_grant_id>31772574</funding_grant_id><pubmed_authors>Dong D</pubmed_authors><pubmed_authors>Li H</pubmed_authors><pubmed_authors>Yang Z</pubmed_authors><pubmed_authors>Yang J</pubmed_authors><pubmed_authors>Huang Y</pubmed_authors><pubmed_authors>Song C</pubmed_authors><pubmed_authors>Ma Y</pubmed_authors><pubmed_authors>Chen H</pubmed_authors><pubmed_authors>Wang J</pubmed_authors><pubmed_authors>Plath M</pubmed_authors></additional><is_claimable>false</is_claimable><name>Linc-smad7 promotes myoblast differentiation and muscle regeneration via sponging miR-125b.</name><description>Long noncoding RNAs (lncRNAs) are involved in the regulation of skeletal muscle development. In the present study, differentially expressed lncRNAs were identified from RNA-seq data derived from myoblasts and myotubes. We conducted studies to elucidate the function and molecular mechanism of action of Linc-smad7 during skeletal muscle development. Our findings show that Linc-smad7 is upregulated during the early phase of myoblasts differentiation. In in vitro studies, we showed that overexpression of Linc-smad7 promoted the arrest of myoblasts in G1 phase, inhibited DNA replication, and induced myoblast differentiation. Our in vivo studies suggest that Linc-smad7 stimulates skeletal muscle regeneration in cardiotoxin-induced muscle injury. Mechanistically, Linc-smad7 overexpression increas</description><dates><release>2018-01-01T00:00:00Z</release><publication>2018</publication><modification>2025-04-04T09:27:07.882Z</modification><creation>2019-08-09T07:02:25Z</creation></dates><accession>S-EPMC6140903</accession><cross_references><pubmed>29912619</pubmed><doi>10.1080/15592294.2018.1481705</doi></cross_references></HashMap>