<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>24(1)</volume><submitter>Wang T</submitter><pubmed_abstract>&lt;h4>Background&lt;/h4>Paenibacillus polymyxa WLY78 is a Gram-positive, endospore-forming and N&lt;sub>2&lt;/sub>-fixing bacterium. Our previous study has demonstrated that GlnR acts as both an activator and a repressor to regulate the transcription of the nif (nitrogen fixation) operon (nifBHDKENXhesAnifV) according to nitrogen availability, which is achieved by binding to the two GlnR-binding sites located in the nif promoter region. However, further study on the GlnR-mediated global regulation in this bacterium is still needed.&lt;h4>Results&lt;/h4>In this study, global identification of the genes directly under GlnR control is determined by using chromatin immunoprecipitation-quantitative PCR (ChIP-qPCR) and electrophoretic mobility shift assays (EMSA). Our results reveal that GlnR directly regulates the transcription of 17 genes/operons, including a nif operon, 14 nitrogen metabolism genes/operons (glnRA, amtBglnK, glnA1, glnK1, glnQHMP, nasA, nasD1, nasD2EF, gcvH, ansZ, pucR, oppABC, appABCDF and dppABC) and 2 carbon metabolism genes (ldh3 and maeA1). Except for the glnRA and nif operon, the other 15 genes/operons are newly identified targets of GlnR. Furthermore, genome-wide transcription analyses reveal that GlnR not only directly regulates the expression of these 17 genes/operons, but also indirectly controls the expression of some other genes/operons involved in nitrogen fixation and the metabolisms of nitrogen and carbon.&lt;h4>Conclusion&lt;/h4>This study provides a GlnR-mediated regulation network of nitrogen fixation and the metabolisms of nitrogen and carbon.</pubmed_abstract><journal>BMC genomics</journal><pagination>85</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC9948412</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Genome-wide mapping of GlnR-binding sites reveals the global regulatory role of GlnR in controlling the metabolism of nitrogen and carbon in Paenibacillus polymyxa WLY78.</pubmed_title><pmcid>PMC9948412</pmcid><pubmed_authors>Wang T</pubmed_authors><pubmed_authors>Chen S</pubmed_authors><pubmed_authors>Zhao X</pubmed_authors><pubmed_authors>Wu X</pubmed_authors></additional><is_claimable>false</is_claimable><name>Genome-wide mapping of GlnR-binding sites reveals the global regulatory role of GlnR in controlling the metabolism of nitrogen and carbon in Paenibacillus polymyxa WLY78.</name><description>&lt;h4>Background&lt;/h4>Paenibacillus polymyxa WLY78 is a Gram-positive, endospore-forming and N&lt;sub>2&lt;/sub>-fixing bacterium. Our previous study has demonstrated that GlnR acts as both an activator and a repressor to regulate the transcription of the nif (nitrogen fixation) operon (nifBHDKENXhesAnifV) according to nitrogen availability, which is achieved by binding to the two GlnR-binding sites located in the nif promoter region. However, further study on the GlnR-mediated global regulation in this bacterium is still needed.&lt;h4>Results&lt;/h4>In this study, global identification of the genes directly under GlnR control is determined by using chromatin immunoprecipitation-quantitative PCR (ChIP-qPCR) and electrophoretic mobility shift assays (EMSA). Our results reveal that GlnR directly regulates the transcription of 17 genes/operons, including a nif operon, 14 nitrogen metabolism genes/operons (glnRA, amtBglnK, glnA1, glnK1, glnQHMP, nasA, nasD1, nasD2EF, gcvH, ansZ, pucR, oppABC, appABCDF and dppABC) and 2 carbon metabolism genes (ldh3 and maeA1). Except for the glnRA and nif operon, the other 15 genes/operons are newly identified targets of GlnR. Furthermore, genome-wide transcription analyses reveal that GlnR not only directly regulates the expression of these 17 genes/operons, but also indirectly controls the expression of some other genes/operons involved in nitrogen fixation and the metabolisms of nitrogen and carbon.&lt;h4>Conclusion&lt;/h4>This study provides a GlnR-mediated regulation network of nitrogen fixation and the metabolisms of nitrogen and carbon.</description><dates><release>2023-01-01T00:00:00Z</release><publication>2023 Feb</publication><modification>2026-05-28T16:55:29.446Z</modification><creation>2025-02-19T02:56:33.776Z</creation></dates><accession>S-EPMC9948412</accession><cross_references><pubmed>36823556</pubmed><doi>10.1186/s12864-023-09147-1</doi></cross_references></HashMap>