<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Sanchez AM</submitter><funding>NSF</funding><funding>NCI NIH HHS</funding><funding>National Institutes of Health</funding><funding>NIH</funding><funding>NIGMS NIH HHS</funding><funding>National Science Foundation</funding><pagination>808-825</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC10187668</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>29(6)</volume><pubmed_abstract>Fission yeast phosphate homeostasis gene &lt;i>pho1&lt;/i> is actively repressed during growth in phosphate-rich medium by transcription in &lt;i>cis&lt;/i> of a long noncoding (lnc) RNA from the 5' flanking &lt;i>prt(nc-pho1)&lt;/i> gene. Pho1 expression is: (i) derepressed by genetic maneuvers that favor precocious lncRNA 3'-processing and termination, in response to DSR and PAS signals in &lt;i>prt&lt;/i>; and (ii) hyperrepressed in genetic backgrounds that dampen 3'-processing/termination efficiency. Governors of 3'-processing/termination include the RNA polymerase CTD code, the CPF (cleavage and polyadenylation factor) complex, termination factors Seb1 and Rhn1, and the inositol pyrophosphate signaling molecule 1,5-IP&lt;sub>8&lt;/sub> Here, we present genetic and biochemical evidence that fission yeast Duf89, a m</pubmed_abstract><journal>RNA (New York, N.Y.)</journal><pubmed_title>Duf89 abets lncRNA control of fission yeast phosphate homeostasis via its antagonism of precocious lncRNA transcription termination.</pubmed_title><pmcid>PMC10187668</pmcid><funding_grant_id>R35 GM126945</funding_grant_id><funding_grant_id>P30 CA008748</funding_grant_id><funding_grant_id>R35-GM126945</funding_grant_id><funding_grant_id>R01-GM134021</funding_grant_id><funding_grant_id>1746057</funding_grant_id><funding_grant_id>R01 GM134021</funding_grant_id><pubmed_authors>Schwer B</pubmed_authors><pubmed_authors>Shuman S</pubmed_authors><pubmed_authors>Garg A</pubmed_authors><pubmed_authors>Sanchez AM</pubmed_authors></additional><is_claimable>false</is_claimable><name>Duf89 abets lncRNA control of fission yeast phosphate homeostasis via its antagonism of precocious lncRNA transcription termination.</name><description>Fission yeast phosphate homeostasis gene &lt;i>pho1&lt;/i> is actively repressed during growth in phosphate-rich medium by transcription in &lt;i>cis&lt;/i> of a long noncoding (lnc) RNA from the 5' flanking &lt;i>prt(nc-pho1)&lt;/i> gene. Pho1 expression is: (i) derepressed by genetic maneuvers that favor precocious lncRNA 3'-processing and termination, in response to DSR and PAS signals in &lt;i>prt&lt;/i>; and (ii) hyperrepressed in genetic backgrounds that dampen 3'-processing/termination efficiency. Governors of 3'-processing/termination include the RNA polymerase CTD code, the CPF (cleavage and polyadenylation factor) complex, termination factors Seb1 and Rhn1, and the inositol pyrophosphate signaling molecule 1,5-IP&lt;sub>8&lt;/sub> Here, we present genetic and biochemical evidence that fission yeast Duf89, a m</description><dates><release>2023-01-01T00:00:00Z</release><publication>2023 Jun</publication><modification>2026-07-15T14:55:49.555Z</modification><creation>2026-07-06T03:09:21.443Z</creation></dates><accession>S-EPMC10187668</accession><cross_references><pubmed>36882296</pubmed><doi>10.1261/rna.079595.123</doi></cross_references></HashMap>