<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Kato M</submitter><funding>NIDDK NIH HHS</funding><funding>National Institute of Diabetes and Digestive and Kidney Diseases</funding><funding>NHLBI NIH HHS</funding><funding>NCI NIH HHS</funding><pagination>1204124</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC10266347</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>10</volume><pubmed_abstract>&lt;b>Background:&lt;/b> MicroRNAs (miRNAs) and long non-coding RNAs (lncRNAs) play key roles in diabetic kidney disease (DKD). The miR-379 megacluster of miRNAs and its host transcript lnc-megacluster (lncMGC) are regulated by transforming growth factor-β (TGF-β), increased in the glomeruli of diabetic mice, and promote features of early DKD. However, biochemical functions of lncMGC are unknown. Here, we identified lncMGC-interacting proteins by &lt;i>in vitro&lt;/i>-transcribed lncMGC RNA pull down followed by mass spectrometry. We also created lncMGC-knockout (KO) mice by CRISPR-Cas9 editing and used primary mouse mesangial cells (MMCs) from the KO mice to examine the effects of lncMGC on the gene expression related to DKD, changes in promoter histone modifications, and chromatin remodeling. &lt;b>Met</pubmed_abstract><journal>Frontiers in molecular biosciences</journal><pubmed_title>Long non-coding RNA lncMGC mediates the expression of TGF-β-induced genes in renal cells via nucleosome remodelers.</pubmed_title><pmcid>PMC10266347</pmcid><funding_grant_id>R01 DK065073</funding_grant_id><funding_grant_id>R01 HL106089</funding_grant_id><funding_grant_id>R01DK081705 R01DK065073 R01HL106089</funding_grant_id><funding_grant_id>P30 CA033572</funding_grant_id><funding_grant_id>R01 DK081705</funding_grant_id><pubmed_authors>Kalkum M</pubmed_authors><pubmed_authors>Abdollahi M</pubmed_authors><pubmed_authors>Das S</pubmed_authors><pubmed_authors>Tsark W</pubmed_authors><pubmed_authors>Moore R</pubmed_authors><pubmed_authors>Wang J</pubmed_authors><pubmed_authors>Lanting L</pubmed_authors><pubmed_authors>Wang M</pubmed_authors><pubmed_authors>Chen Z</pubmed_authors><pubmed_authors>Kato M</pubmed_authors><pubmed_authors>Chen W</pubmed_authors><pubmed_authors>Li A</pubmed_authors><pubmed_authors>Tunduguru R</pubmed_authors><pubmed_authors>Natarajan R</pubmed_authors><pubmed_authors>Wu X</pubmed_authors></additional><is_claimable>false</is_claimable><name>Long non-coding RNA lncMGC mediates the expression of TGF-β-induced genes in renal cells via nucleosome remodelers.</name><description>&lt;b>Background:&lt;/b> MicroRNAs (miRNAs) and long non-coding RNAs (lncRNAs) play key roles in diabetic kidney disease (DKD). The miR-379 megacluster of miRNAs and its host transcript lnc-megacluster (lncMGC) are regulated by transforming growth factor-β (TGF-β), increased in the glomeruli of diabetic mice, and promote features of early DKD. However, biochemical functions of lncMGC are unknown. Here, we identified lncMGC-interacting proteins by &lt;i>in vitro&lt;/i>-transcribed lncMGC RNA pull down followed by mass spectrometry. We also created lncMGC-knockout (KO) mice by CRISPR-Cas9 editing and used primary mouse mesangial cells (MMCs) from the KO mice to examine the effects of lncMGC on the gene expression related to DKD, changes in promoter histone modifications, and chromatin remodeling. &lt;b>Met</description><dates><release>2023-01-01T00:00:00Z</release><publication>2023</publication><modification>2026-05-29T19:26:01.376Z</modification><creation>2024-11-12T22:04:24.195Z</creation></dates><accession>S-EPMC10266347</accession><cross_references><pubmed>37325470</pubmed><doi>10.3389/fmolb.2023.1204124</doi></cross_references></HashMap>