<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Koster KA</submitter><funding>Deutsche Forschungsgemeinschaft</funding><funding>Universitätsklinikum Hamburg-Eppendorf (UKE)</funding><pagination>1223-1233</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC10185614</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>396(6)</volume><pubmed_abstract>The dual leucine zipper kinase (DLK) and the ubiquitously expressed transcription factor c-FOS have important roles in beta-cell proliferation and function. Some studies in neuronal cells suggest that DLK can influence c-FOS expression. Given that c-FOS is mainly regulated at the transcriptional level, the effect of DLK on c-FOS promoter activity was investigated in the beta-cell line HIT. The methods used in this study are the following: Luciferase reporter gene assays, immunoblot analysis, CRISPR-Cas9-mediated genome editing, and real-time quantitative PCR. In the beta-cell line HIT, overexpressed DLK increased c-FOS promoter activity twofold. Using 5'-,3'-promoter deletions, the promoter regions from - 348 to - 339 base pairs (bp) and from a - 284 to - 53 bp conferred basal activity, wh</pubmed_abstract><journal>Naunyn-Schmiedeberg's archives of pharmacology</journal><pubmed_title>Increase of c-FOS promoter transcriptional activity by the dual leucine zipper kinase.</pubmed_title><pmcid>PMC10185614</pmcid><funding_grant_id>OE 181/5-1</funding_grant_id><pubmed_authors>Duque Escobar J</pubmed_authors><pubmed_authors>Toledo R</pubmed_authors><pubmed_authors>Oetjen E</pubmed_authors><pubmed_authors>Fietkau A</pubmed_authors><pubmed_authors>Koster KA</pubmed_authors></additional><is_claimable>false</is_claimable><name>Increase of c-FOS promoter transcriptional activity by the dual leucine zipper kinase.</name><description>The dual leucine zipper kinase (DLK) and the ubiquitously expressed transcription factor c-FOS have important roles in beta-cell proliferation and function. Some studies in neuronal cells suggest that DLK can influence c-FOS expression. Given that c-FOS is mainly regulated at the transcriptional level, the effect of DLK on c-FOS promoter activity was investigated in the beta-cell line HIT. The methods used in this study are the following: Luciferase reporter gene assays, immunoblot analysis, CRISPR-Cas9-mediated genome editing, and real-time quantitative PCR. In the beta-cell line HIT, overexpressed DLK increased c-FOS promoter activity twofold. Using 5'-,3'-promoter deletions, the promoter regions from - 348 to - 339 base pairs (bp) and from a - 284 to - 53 bp conferred basal activity, wh</description><dates><release>2023-01-01T00:00:00Z</release><publication>2023 Jun</publication><modification>2025-04-26T17:23:44.237Z</modification><creation>2025-04-06T15:33:19.22Z</creation></dates><accession>S-EPMC10185614</accession><cross_references><pubmed>36700987</pubmed><doi>10.1007/s00210-023-02401-z</doi></cross_references></HashMap>