<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>28</volume><submitter>Hirata CL</submitter><funding>Japan Society for the Promotion of Science</funding><pubmed_abstract>This dataset is supplementary to the submitted research by Ref. [1]. RNAs were extracted from high molecular weight complexes, prepared with 100 kDa filtration of HEK293 Tet-on cells stably transfected with either F-HA-Txnip-V5-His or control vector. Cells were stimulated with 1 μg/mL doxycycline for 24 h, followed by overnight stimulation with 100 μM 4-thiouridine (4sU), 20 mM glucose, and 1 μM bortezomib for 14h. The extracted RNAs from Txnip overexpressing cells compared with control cells was analyzed by RNA-seq. Differentially expressed mRNAs, long noncoding RNAs (lncRNA) and transcripts of uncertain coding potential (TUCPs) are shown. Gene ontology and KEGG enrichment of these differential expressed RNAs is presented.</pubmed_abstract><journal>Data in brief</journal><pagination>104893</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC6926129</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Dataset on the formation of Thioredoxin interacting protein (Txnip) containing redox sensitive high molecular weight nucleoprotein complexes.</pubmed_title><pmcid>PMC6926129</pmcid><pubmed_authors>Masutani H</pubmed_authors><pubmed_authors>Hirata CL</pubmed_authors><pubmed_authors>Ito S</pubmed_authors></additional><is_claimable>false</is_claimable><name>Dataset on the formation of Thioredoxin interacting protein (Txnip) containing redox sensitive high molecular weight nucleoprotein complexes.</name><description>This dataset is supplementary to the submitted research by Ref. [1]. RNAs were extracted from high molecular weight complexes, prepared with 100 kDa filtration of HEK293 Tet-on cells stably transfected with either F-HA-Txnip-V5-His or control vector. Cells were stimulated with 1 μg/mL doxycycline for 24 h, followed by overnight stimulation with 100 μM 4-thiouridine (4sU), 20 mM glucose, and 1 μM bortezomib for 14h. The extracted RNAs from Txnip overexpressing cells compared with control cells was analyzed by RNA-seq. Differentially expressed mRNAs, long noncoding RNAs (lncRNA) and transcripts of uncertain coding potential (TUCPs) are shown. Gene ontology and KEGG enrichment of these differential expressed RNAs is presented.</description><dates><release>2020-01-01T00:00:00Z</release><publication>2020 Feb</publication><modification>2024-12-04T12:06:38.342Z</modification><creation>2020-05-22T01:16:02Z</creation></dates><accession>S-EPMC6926129</accession><cross_references><pubmed>31890777</pubmed><doi>10.1016/j.dib.2019.104893</doi></cross_references></HashMap>