<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Viegas IJ</submitter><funding>NINDS NIH HHS</funding><funding>NCI NIH HHS</funding><funding>Engineering and Physical Sciences Research Council</funding><pagination>362-370</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC9150445</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>604(7905)</volume><pubmed_abstract>RNA modifications are important regulators of gene expression&lt;sup>1&lt;/sup>. In Trypanosoma brucei, transcription is polycistronic and thus most regulation happens post-transcriptionally&lt;sup>2&lt;/sup>. N&lt;sup>6&lt;/sup>-methyladenosine (m&lt;sup>6&lt;/sup>A) has been detected in this parasite, but its function remains unknown&lt;sup>3&lt;/sup>. Here we found that m&lt;sup>6&lt;/sup>A is enriched in 342 transcripts using RNA immunoprecipitation, with an enrichment in transcripts encoding variant surface glycoproteins (VSGs). Approximately 50% of the m&lt;sup>6&lt;/sup>A is located in the poly(A) tail of the actively expressed VSG transcripts. m&lt;sup>6&lt;/sup>A residues are removed from the VSG poly(A) tail before deadenylation and mRNA degradation. Computational analysis revealed an association between m&lt;sup>6&lt;/sup>A in the </pubmed_abstract><journal>Nature</journal><pubmed_title>N&lt;sup>6&lt;/sup>-methyladenosine in poly(A) tails stabilize VSG transcripts.</pubmed_title><pmcid>PMC9150445</pmcid><funding_grant_id>T32 CA062948</funding_grant_id><funding_grant_id>R35 NS111631</funding_grant_id><funding_grant_id>EP/K039660/1</funding_grant_id><funding_grant_id>EP/M028127/1</funding_grant_id><pubmed_authors>De Niz M</pubmed_authors><pubmed_authors>Serra L</pubmed_authors><pubmed_authors>Silva Pereira S</pubmed_authors><pubmed_authors>Viegas IJ</pubmed_authors><pubmed_authors>Temporao A</pubmed_authors><pubmed_authors>Bergstrom E</pubmed_authors><pubmed_authors>Figueiredo LM</pubmed_authors><pubmed_authors>Aresta-Branco F</pubmed_authors><pubmed_authors>Jaffrey SR</pubmed_authors><pubmed_authors>de Macedo JP</pubmed_authors><pubmed_authors>Mirza AH</pubmed_authors><pubmed_authors>Rodrigues JA</pubmed_authors></additional><is_claimable>false</is_claimable><name>N&lt;sup>6&lt;/sup>-methyladenosine in poly(A) tails stabilize VSG transcripts.</name><description>RNA modifications are important regulators of gene expression&lt;sup>1&lt;/sup>. In Trypanosoma brucei, transcription is polycistronic and thus most regulation happens post-transcriptionally&lt;sup>2&lt;/sup>. N&lt;sup>6&lt;/sup>-methyladenosine (m&lt;sup>6&lt;/sup>A) has been detected in this parasite, but its function remains unknown&lt;sup>3&lt;/sup>. Here we found that m&lt;sup>6&lt;/sup>A is enriched in 342 transcripts using RNA immunoprecipitation, with an enrichment in transcripts encoding variant surface glycoproteins (VSGs). Approximately 50% of the m&lt;sup>6&lt;/sup>A is located in the poly(A) tail of the actively expressed VSG transcripts. m&lt;sup>6&lt;/sup>A residues are removed from the VSG poly(A) tail before deadenylation and mRNA degradation. Computational analysis revealed an association between m&lt;sup>6&lt;/sup>A in the </description><dates><release>2022-01-01T00:00:00Z</release><publication>2022 Apr</publication><modification>2025-04-04T12:05:11.193Z</modification><creation>2025-04-04T12:05:11.193Z</creation></dates><accession>S-EPMC9150445</accession><cross_references><pubmed>35355019</pubmed><doi>10.1038/s41586-022-04544-0</doi></cross_references></HashMap>