<HashMap><database>biostudies-other</database><scores/><additional><omics_type>Unknown</omics_type><volume>90(24)</volume><submitter>McMillan JP</submitter><journal>Proceedings of the National Academy of Sciences of the United States of America</journal><pagination>11533-7</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC48018</full_dataset_link><abstract>Full-length RNA transcribed from the human LINE-1 (L1) element L1 Homo sapiens (L1Hs) has a 900-nt, G+C-rich, 5'-untranslated region (UTR). The 5' UTR is followed by two long open reading frames, ORF1 and ORF2, which are separated from each other by an inter-ORF region of 33 nt that includes two or three in-frame stop codons. We examine here the mechanism(s) by which the translation of L1Hs ORF1 and ORF2 is initiated. A stable hairpin structure (delta G = -74.8 kcal/mol), inserted at nt 661 of the 5' UTR, caused a 3- to 8-fold decrease in the in vitro and in vivo translation of either a lacZ reporter gene for ORF1 or the ORF1 polypeptide product, p40, but translation of a lacZ reporter gene in ORF2 was increased. The results are compatible with a model for ORF1 translation initiation in which the majority of ribosomes scan from a point 5' of nt 661 but suggest that ORF2 is not translated by attached ribosomes that reinitiate after the termination of ORF1 translation. Our data are compatible with a model whereby the translation of L1Hs ORF2 is initiated internally.</abstract><repository>biostudies-other</repository><pmcid>PMC48018</pmcid><data_source>Europe PMC</data_source><pubmed_authors>McMillan JP</pubmed_authors><pubmed_authors>Singer MF</pubmed_authors></additional><is_claimable>false</is_claimable><name>Translation of the human LINE-1 element, L1Hs.</name><description>Full-length RNA transcribed from the human LINE-1 (L1) element L1 Homo sapiens (L1Hs) has a 900-nt, G+C-rich, 5'-untranslated region (UTR). The 5' UTR is followed by two long open reading frames, ORF1 and ORF2, which are separated from each other by an inter-ORF region of 33 nt that includes two or three in-frame stop codons. We examine here the mechanism(s) by which the translation of L1Hs ORF1 and ORF2 is initiated. A stable hairpin structure (delta G = -74.8 kcal/mol), inserted at nt 661 of the 5' UTR, caused a 3- to 8-fold decrease in the in vitro and in vivo translation of either a lacZ reporter gene for ORF1 or the ORF1 polypeptide product, p40, but translation of a lacZ reporter gene in ORF2 was increased. The results are compatible with a model for ORF1 translation initiation in which the majority of ribosomes scan from a point 5' of nt 661 but suggest that ORF2 is not translated by attached ribosomes that reinitiate after the termination of ORF1 translation. Our data are compatible with a model whereby the translation of L1Hs ORF2 is initiated internally.</description><dates><release>1993-01-01T00:00:00Z</release><publication>1993 Dec</publication><modification>2019-03-27T00:18:08Z</modification><creation>2019-03-27T00:18:08Z</creation></dates><accession>S-EPMC48018</accession><cross_references><gen>M80343</gen><pubmed>8265584</pubmed><doi>10.1073/pnas.90.24.11533 </doi></cross_references></HashMap>