<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Ciganda M</submitter><funding>NIAID NIH HHS</funding><funding>PEDECIBA and are members of ANII research career</funding><funding>NIH</funding><pagination>1881-1895</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC10653379</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>29(12)</volume><pubmed_abstract>&lt;i>Trypanosoma brucei&lt;/i> occupies distinct niches throughout its life cycle, within both the mammalian and tsetse fly hosts. The immunological and biochemical complexity and variability of each of these environments require a reshaping of the protein landscape of the parasite both to evade surveillance and face changing metabolic demands. In kinetoplastid protozoa, including &lt;i>T. brucei&lt;/i>, posttranscriptional control mechanisms are the primary means of gene regulation, and these are often mediated by RNA-binding proteins. DRBD18 is a &lt;i>T. brucei&lt;/i> RNA-binding protein that reportedly interacts with ribosomal proteins and translation factors. Here, we tested a role for DRBD18 in translational control. We validate the DRBD18 interaction with translating ribosomes and the translation in</pubmed_abstract><journal>RNA (New York, N.Y.)</journal><pubmed_title>Translational control by &lt;i>Trypanosoma brucei&lt;/i> DRBD18 contributes to the maintenance of the procyclic state.</pubmed_title><pmcid>PMC10653379</pmcid><funding_grant_id>R01AI141557</funding_grant_id><funding_grant_id>R01 AI141557</funding_grant_id><pubmed_authors>Dubey AP</pubmed_authors><pubmed_authors>Ciganda M</pubmed_authors><pubmed_authors>Smircich P</pubmed_authors><pubmed_authors>Read LK</pubmed_authors><pubmed_authors>Qu J</pubmed_authors><pubmed_authors>Shen S</pubmed_authors><pubmed_authors>Pandey P</pubmed_authors><pubmed_authors>Sotelo-Silveira J</pubmed_authors><pubmed_authors>Smith JT</pubmed_authors></additional><is_claimable>false</is_claimable><name>Translational control by &lt;i>Trypanosoma brucei&lt;/i> DRBD18 contributes to the maintenance of the procyclic state.</name><description>&lt;i>Trypanosoma brucei&lt;/i> occupies distinct niches throughout its life cycle, within both the mammalian and tsetse fly hosts. The immunological and biochemical complexity and variability of each of these environments require a reshaping of the protein landscape of the parasite both to evade surveillance and face changing metabolic demands. In kinetoplastid protozoa, including &lt;i>T. brucei&lt;/i>, posttranscriptional control mechanisms are the primary means of gene regulation, and these are often mediated by RNA-binding proteins. DRBD18 is a &lt;i>T. brucei&lt;/i> RNA-binding protein that reportedly interacts with ribosomal proteins and translation factors. Here, we tested a role for DRBD18 in translational control. We validate the DRBD18 interaction with translating ribosomes and the translation in</description><dates><release>2023-01-01T00:00:00Z</release><publication>2023 Dec</publication><modification>2025-04-04T09:50:05.155Z</modification><creation>2025-02-19T01:17:08.382Z</creation></dates><accession>S-EPMC10653379</accession><cross_references><pubmed>37730435</pubmed><doi>10.1261/rna.079625.123</doi></cross_references></HashMap>