<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Wang H</submitter><funding>Texas Crop Science</funding><pagination>3514</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC12656381</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>14(22)</volume><pubmed_abstract>As reported in earlier work, when a pea apyrase, psNTP9 (PS), and a modified version of it, psNTP9-DM (DM), are expressed in &lt;i>Saccharomyces cerevisiae&lt;/i>, they localize to nuclei, binding to largely non-overlapping promoter regions of chromatin. PS- and DM-expressing yeast also exhibit different expression profiles for potentially regulated target genes, consistent with observed phenotypes. In the present study, we use ChIP-seq assays to show that PS and DM also associate with largely different promoter regions of Arabidopsis genes, with similar non-overlapping expression profiles for potential target genes. Functional studies, using electrophoretic mobility shift assays (EMSA), verified PS-specific binding to yeast or plant promoter binding sites. DM binding to both heterologous dsDNA </pubmed_abstract><journal>Plants (Basel, Switzerland)</journal><pubmed_title>Chromatin-Associated Pea Apyrase psNTP9 Function as a DNA-Binding Regulatory Protein in Yeast and Arabidopsis.</pubmed_title><pmcid>PMC12656381</pmcid><funding_grant_id>UTA13-000682</funding_grant_id><pubmed_authors>Clark G</pubmed_authors><pubmed_authors>Roux SJ</pubmed_authors><pubmed_authors>Slocum RD</pubmed_authors><pubmed_authors>Wang H</pubmed_authors><pubmed_authors>Cai X</pubmed_authors></additional><is_claimable>false</is_claimable><name>Chromatin-Associated Pea Apyrase psNTP9 Function as a DNA-Binding Regulatory Protein in Yeast and Arabidopsis.</name><description>As reported in earlier work, when a pea apyrase, psNTP9 (PS), and a modified version of it, psNTP9-DM (DM), are expressed in &lt;i>Saccharomyces cerevisiae&lt;/i>, they localize to nuclei, binding to largely non-overlapping promoter regions of chromatin. PS- and DM-expressing yeast also exhibit different expression profiles for potentially regulated target genes, consistent with observed phenotypes. In the present study, we use ChIP-seq assays to show that PS and DM also associate with largely different promoter regions of Arabidopsis genes, with similar non-overlapping expression profiles for potential target genes. Functional studies, using electrophoretic mobility shift assays (EMSA), verified PS-specific binding to yeast or plant promoter binding sites. DM binding to both heterologous dsDNA </description><dates><release>2025-01-01T00:00:00Z</release><publication>2025 Nov</publication><modification>2026-07-05T03:18:22.822Z</modification><creation>2026-07-05T03:12:28.097Z</creation></dates><accession>S-EPMC12656381</accession><cross_references><pubmed>41304665</pubmed><doi>10.3390/plants14223514</doi></cross_references></HashMap>