<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Wang S</submitter><funding>the China Postdoctoral Science Foundation</funding><funding>the Guangdong Basic and Applied Basic Research Fund: Regional Joint Fund-Youth Fund Project</funding><pagination>4600</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC9105514</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>23(9)</volume><pubmed_abstract>N&lt;sup>6&lt;/sup>-methyladenosine (m&lt;sup>6&lt;/sup>A) is the most common modification in eukaryotic RNAs. Accumulating evidence shows m&lt;sup>6&lt;/sup>A methylation plays vital roles in various biological processes, including muscle and fat differentiation. However, there is a lack of research on lncRNAs' m&lt;sup>6&lt;/sup>A modification in regulating pig muscle-fiber-type conversion. In this study, we identified novel and differentially expressed lncRNAs in oxidative and glycolytic skeletal muscles through RNA-seq, and further reported the m&lt;sup>6&lt;/sup>A-methylation patterns of lncRNAs via MeRIP-seq. We found that most lncRNAs have one m&lt;sup>6&lt;/sup>A peak, and the m&lt;sup>6&lt;/sup>A peaks were preferentially enriched in the last exon of the lncRNAs. Interestingly, we found that lncRNAs' m&lt;sup>6&lt;/sup>A levels were positively correlated with their expression homeostasis and levels. Furthermore, we performed conjoint analysis of MeRIP-seq and RNA-seq data and obtained 305 differentially expressed and differentially m&lt;sup>6&lt;/sup>A-modified lncRNAs (dme-lncRNAs). Through QTL enrichment analysis of dme-lncRNAs and PPI analysis for their cis-genes, we finally identified seven key m&lt;sup>6&lt;/sup>A-modified lncRNAs that may play a potential role in muscle-fiber-type conversion. Notably, inhibition of one of the key lncRNAs, &lt;i>MSTRG.14200.1&lt;/i>, delayed satellite cell differentiation and stimulated fast-to-slow muscle-fiber conversion. Our study comprehensively analyzed m&lt;sup>6&lt;/sup>A modifications on lncRNAs in oxidative and glycolytic skeletal muscles and provided new targets for the study of pig muscle-fiber-type conversion.</pubmed_abstract><journal>International journal of molecular sciences</journal><pubmed_title>Comprehensive Analysis of Long Noncoding RNA Modified by m&lt;sup>6&lt;/sup>A Methylation in Oxidative and Glycolytic Skeletal Muscles.</pubmed_title><pmcid>PMC9105514</pmcid><funding_grant_id>2020A1515110319</funding_grant_id><funding_grant_id>2021M691075</funding_grant_id><pubmed_authors>Hong L</pubmed_authors><pubmed_authors>Gu T</pubmed_authors><pubmed_authors>Wu Z</pubmed_authors><pubmed_authors>Yang J</pubmed_authors><pubmed_authors>Xiao L</pubmed_authors><pubmed_authors>Wang S</pubmed_authors><pubmed_authors>Zeng J</pubmed_authors><pubmed_authors>Tan B</pubmed_authors><pubmed_authors>Zheng E</pubmed_authors><pubmed_authors>Zhao X</pubmed_authors><pubmed_authors>Cai G</pubmed_authors></additional><is_claimable>false</is_claimable><name>Comprehensive Analysis of Long Noncoding RNA Modified by m&lt;sup>6&lt;/sup>A Methylation in Oxidative and Glycolytic Skeletal Muscles.</name><description>N&lt;sup>6&lt;/sup>-methyladenosine (m&lt;sup>6&lt;/sup>A) is the most common modification in eukaryotic RNAs. Accumulating evidence shows m&lt;sup>6&lt;/sup>A methylation plays vital roles in various biological processes, including muscle and fat differentiation. However, there is a lack of research on lncRNAs' m&lt;sup>6&lt;/sup>A modification in regulating pig muscle-fiber-type conversion. In this study, we identified novel and differentially expressed lncRNAs in oxidative and glycolytic skeletal muscles through RNA-seq, and further reported the m&lt;sup>6&lt;/sup>A-methylation patterns of lncRNAs via MeRIP-seq. We found that most lncRNAs have one m&lt;sup>6&lt;/sup>A peak, and the m&lt;sup>6&lt;/sup>A peaks were preferentially enriched in the last exon of the lncRNAs. Interestingly, we found that lncRNAs' m&lt;sup>6&lt;/sup>A levels were positively correlated with their expression homeostasis and levels. Furthermore, we performed conjoint analysis of MeRIP-seq and RNA-seq data and obtained 305 differentially expressed and differentially m&lt;sup>6&lt;/sup>A-modified lncRNAs (dme-lncRNAs). Through QTL enrichment analysis of dme-lncRNAs and PPI analysis for their cis-genes, we finally identified seven key m&lt;sup>6&lt;/sup>A-modified lncRNAs that may play a potential role in muscle-fiber-type conversion. Notably, inhibition of one of the key lncRNAs, &lt;i>MSTRG.14200.1&lt;/i>, delayed satellite cell differentiation and stimulated fast-to-slow muscle-fiber conversion. Our study comprehensively analyzed m&lt;sup>6&lt;/sup>A modifications on lncRNAs in oxidative and glycolytic skeletal muscles and provided new targets for the study of pig muscle-fiber-type conversion.</description><dates><release>2022-01-01T00:00:00Z</release><publication>2022 Apr</publication><modification>2025-04-22T11:49:39.872Z</modification><creation>2025-02-19T03:41:46.46Z</creation></dates><accession>S-EPMC9105514</accession><cross_references><pubmed>35562992</pubmed><doi>10.3390/ijms23094600</doi></cross_references></HashMap>