<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>14(1)</volume><submitter>Dahl LD</submitter><pubmed_abstract>&lt;h4>Background&lt;/h4>The oncogene PTI-1 was originally isolated from a prostate cancer cell line by its capability to transform rat fibroblasts. The PTI-1 mRNA has a very eccentric structure as the 5'UTR is similar to prokaryotic 23S rRNA, while the major open reading frame and the 3'UTR corresponds to a part of the mRNA encoding human translation elongation factor eEF1A1. Thus, the largest open reading frame encodes a truncated version of eEF1A1 lacking the first 67 amino acids, while having three unique N-terminal amino acids. Previously, the UTRs were shown to be a prerequisite for the transforming capacity of the PTI-1 transcript. In this study, we have investigated the possible role of the UTRs in regulating protein expression and localization.&lt;h4>Methods&lt;/h4>The protein expression prof</pubmed_abstract><journal>Cancer cell international</journal><pagination>17</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC3941776</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>An eEF1A1 truncation encoded by PTI-1 exerts its oncogenic effect inside the nucleus.</pubmed_title><pmcid>PMC3941776</pmcid><pubmed_authors>Nielsen KM</pubmed_authors><pubmed_authors>Fuchtbauer EM</pubmed_authors><pubmed_authors>Corydon TJ</pubmed_authors><pubmed_authors>Knudsen CR</pubmed_authors><pubmed_authors>Rankel L</pubmed_authors><pubmed_authors>Dahl LD</pubmed_authors></additional><is_claimable>false</is_claimable><name>An eEF1A1 truncation encoded by PTI-1 exerts its oncogenic effect inside the nucleus.</name><description>&lt;h4>Background&lt;/h4>The oncogene PTI-1 was originally isolated from a prostate cancer cell line by its capability to transform rat fibroblasts. The PTI-1 mRNA has a very eccentric structure as the 5'UTR is similar to prokaryotic 23S rRNA, while the major open reading frame and the 3'UTR corresponds to a part of the mRNA encoding human translation elongation factor eEF1A1. Thus, the largest open reading frame encodes a truncated version of eEF1A1 lacking the first 67 amino acids, while having three unique N-terminal amino acids. Previously, the UTRs were shown to be a prerequisite for the transforming capacity of the PTI-1 transcript. In this study, we have investigated the possible role of the UTRs in regulating protein expression and localization.&lt;h4>Methods&lt;/h4>The protein expression prof</description><dates><release>2014-01-01T00:00:00Z</release><publication>2014 Feb</publication><modification>2025-05-18T11:42:01.105Z</modification><creation>2025-05-18T11:42:01.105Z</creation></dates><accession>S-EPMC3941776</accession><cross_references><pubmed>24571548</pubmed><doi>10.1186/1475-2867-14-17</doi></cross_references></HashMap>