Upstream ORFs influence translation efficiency in the parasite Trypanosoma cruzi
Editor(es): Katz, A.
Resumen:
It is generally accepted that the presence of ORFs in the 5′ untranslated region of eukaryotic transcripts modulates the production of proteins by controlling the translation initiation rate of the main CDS. In trypanosomatid parasites, which almost exclusively depend on post-transcriptional mechanisms to regulate gene expression, translation has been identified as a key step. However, the mechanisms of control of translation are not fully understood. In the present work, we have annotated the 5′UTRs of the Trypanosoma cruzi genome both in epimastigotes and metacyclic trypomastigotes and, using a stringent classification approach, we identified putative regulatory uORFs in about 9% of the analyzed 5′UTRs. The translation efficiency (TE) and translational levels of transcripts containing putative repressive uORFs were found to be significantly reduced. These findings are supported by the fact that proteomic methods only identify a low number of proteins coded by transcripts containing repressive uORF. We additionally show that AUG is the main translation initiator codon of repressive uORFs in T. cruzi. Interestingly, the decrease in TE is more pronounced when the uORFs overlaps the main CDS. In conclusion, we show that the presence of the uORF and features such as initiation codon and/or location of the uORFs may be acting to fine tune translation levels in these parasites.
2020 | |
Trypanosoma cruzi uORF 50UTR Translation efficiency Translation regulation |
|
Inglés | |
Universidad de la República | |
COLIBRI | |
https://hdl.handle.net/20.500.12008/32361 | |
Acceso abierto | |
Licencia Creative Commons Atribución (CC - By 4.0) |
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---|---|
author | Radío, Santiago |
author2 | Garat, Beatriz Sotelo Silveira, José Roberto Smircich, Pablo |
author2_role | author author author |
author_facet | Radío, Santiago Garat, Beatriz Sotelo Silveira, José Roberto Smircich, Pablo |
author_role | author |
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collection | COLIBRI |
dc.contributor.filiacion.none.fl_str_mv | Radío Santiago, Universidad de la República (Uruguay). Facultad de Ciencias. Instituto de Biología. Garat Beatriz, Universidad de la República (Uruguay). Facultad de Ciencias. Instituto de Biología. Sotelo Silveira José Roberto, Universidad de la República (Uruguay). Facultad de Ciencias. Instituto de Biología. Smircich Pablo, Universidad de la República (Uruguay). Facultad de Ciencias. Instituto de Biología. |
dc.creator.editor.none.fl_str_mv | Katz, A. |
dc.creator.none.fl_str_mv | Radío, Santiago Garat, Beatriz Sotelo Silveira, José Roberto Smircich, Pablo |
dc.date.accessioned.none.fl_str_mv | 2022-06-24T13:24:43Z |
dc.date.available.none.fl_str_mv | 2022-06-24T13:24:43Z |
dc.date.issued.none.fl_str_mv | 2020 |
dc.description.abstract.none.fl_txt_mv | It is generally accepted that the presence of ORFs in the 5′ untranslated region of eukaryotic transcripts modulates the production of proteins by controlling the translation initiation rate of the main CDS. In trypanosomatid parasites, which almost exclusively depend on post-transcriptional mechanisms to regulate gene expression, translation has been identified as a key step. However, the mechanisms of control of translation are not fully understood. In the present work, we have annotated the 5′UTRs of the Trypanosoma cruzi genome both in epimastigotes and metacyclic trypomastigotes and, using a stringent classification approach, we identified putative regulatory uORFs in about 9% of the analyzed 5′UTRs. The translation efficiency (TE) and translational levels of transcripts containing putative repressive uORFs were found to be significantly reduced. These findings are supported by the fact that proteomic methods only identify a low number of proteins coded by transcripts containing repressive uORF. We additionally show that AUG is the main translation initiator codon of repressive uORFs in T. cruzi. Interestingly, the decrease in TE is more pronounced when the uORFs overlaps the main CDS. In conclusion, we show that the presence of the uORF and features such as initiation codon and/or location of the uORFs may be acting to fine tune translation levels in these parasites. |
dc.format.extent.es.fl_str_mv | 9 h. |
dc.format.mimetype.es.fl_str_mv | application/pdf |
dc.identifier.citation.es.fl_str_mv | Radío, S, Garat, B, Sotelo Silveira, J [y otros] "Upstream ORFs influence translation efficiency in the parasite Trypanosoma cruzi". Frontiers in Genetics. [en línea] 2020, 11:166. 9 h. DOI: 10.3389/fgene.2020.00166 |
dc.identifier.doi.none.fl_str_mv | 10.3389/fgene.2020.00166 |
dc.identifier.issn.none.fl_str_mv | 1664-8021 |
dc.identifier.uri.none.fl_str_mv | https://hdl.handle.net/20.500.12008/32361 |
dc.language.iso.none.fl_str_mv | en eng |
dc.publisher.es.fl_str_mv | Frontiers Media |
dc.relation.ispartof.es.fl_str_mv | Frontiers in Genetics, 2020, 11:166 |
dc.rights.license.none.fl_str_mv | Licencia Creative Commons Atribución (CC - By 4.0) |
dc.rights.none.fl_str_mv | info:eu-repo/semantics/openAccess |
dc.source.none.fl_str_mv | reponame:COLIBRI instname:Universidad de la República instacron:Universidad de la República |
dc.subject.es.fl_str_mv | Trypanosoma cruzi uORF 50UTR Translation efficiency Translation regulation |
dc.title.none.fl_str_mv | Upstream ORFs influence translation efficiency in the parasite Trypanosoma cruzi |
dc.type.es.fl_str_mv | Artículo |
dc.type.none.fl_str_mv | info:eu-repo/semantics/article |
dc.type.version.none.fl_str_mv | info:eu-repo/semantics/publishedVersion |
description | It is generally accepted that the presence of ORFs in the 5′ untranslated region of eukaryotic transcripts modulates the production of proteins by controlling the translation initiation rate of the main CDS. In trypanosomatid parasites, which almost exclusively depend on post-transcriptional mechanisms to regulate gene expression, translation has been identified as a key step. However, the mechanisms of control of translation are not fully understood. In the present work, we have annotated the 5′UTRs of the Trypanosoma cruzi genome both in epimastigotes and metacyclic trypomastigotes and, using a stringent classification approach, we identified putative regulatory uORFs in about 9% of the analyzed 5′UTRs. The translation efficiency (TE) and translational levels of transcripts containing putative repressive uORFs were found to be significantly reduced. These findings are supported by the fact that proteomic methods only identify a low number of proteins coded by transcripts containing repressive uORF. We additionally show that AUG is the main translation initiator codon of repressive uORFs in T. cruzi. Interestingly, the decrease in TE is more pronounced when the uORFs overlaps the main CDS. In conclusion, we show that the presence of the uORF and features such as initiation codon and/or location of the uORFs may be acting to fine tune translation levels in these parasites. |
eu_rights_str_mv | openAccess |
format | article |
id | COLIBRI_d6ef1b910eed22180fb4bdb49c6bd969 |
identifier_str_mv | Radío, S, Garat, B, Sotelo Silveira, J [y otros] "Upstream ORFs influence translation efficiency in the parasite Trypanosoma cruzi". Frontiers in Genetics. [en línea] 2020, 11:166. 9 h. DOI: 10.3389/fgene.2020.00166 1664-8021 10.3389/fgene.2020.00166 |
instacron_str | Universidad de la República |
institution | Universidad de la República |
instname_str | Universidad de la República |
language | eng |
language_invalid_str_mv | en |
network_acronym_str | COLIBRI |
network_name_str | COLIBRI |
oai_identifier_str | oai:colibri.udelar.edu.uy:20.500.12008/32361 |
publishDate | 2020 |
reponame_str | COLIBRI |
repository.mail.fl_str_mv | mabel.seroubian@seciu.edu.uy |
repository.name.fl_str_mv | COLIBRI - Universidad de la República |
repository_id_str | 4771 |
rights_invalid_str_mv | Licencia Creative Commons Atribución (CC - By 4.0) |
spelling | Radío Santiago, Universidad de la República (Uruguay). Facultad de Ciencias. Instituto de Biología.Garat Beatriz, Universidad de la República (Uruguay). Facultad de Ciencias. Instituto de Biología.Sotelo Silveira José Roberto, Universidad de la República (Uruguay). Facultad de Ciencias. Instituto de Biología.Smircich Pablo, Universidad de la República (Uruguay). Facultad de Ciencias. Instituto de Biología.2022-06-24T13:24:43Z2022-06-24T13:24:43Z2020Radío, S, Garat, B, Sotelo Silveira, J [y otros] "Upstream ORFs influence translation efficiency in the parasite Trypanosoma cruzi". Frontiers in Genetics. [en línea] 2020, 11:166. 9 h. DOI: 10.3389/fgene.2020.001661664-8021https://hdl.handle.net/20.500.12008/3236110.3389/fgene.2020.00166It is generally accepted that the presence of ORFs in the 5′ untranslated region of eukaryotic transcripts modulates the production of proteins by controlling the translation initiation rate of the main CDS. In trypanosomatid parasites, which almost exclusively depend on post-transcriptional mechanisms to regulate gene expression, translation has been identified as a key step. However, the mechanisms of control of translation are not fully understood. In the present work, we have annotated the 5′UTRs of the Trypanosoma cruzi genome both in epimastigotes and metacyclic trypomastigotes and, using a stringent classification approach, we identified putative regulatory uORFs in about 9% of the analyzed 5′UTRs. The translation efficiency (TE) and translational levels of transcripts containing putative repressive uORFs were found to be significantly reduced. These findings are supported by the fact that proteomic methods only identify a low number of proteins coded by transcripts containing repressive uORF. We additionally show that AUG is the main translation initiator codon of repressive uORFs in T. cruzi. Interestingly, the decrease in TE is more pronounced when the uORFs overlaps the main CDS. In conclusion, we show that the presence of the uORF and features such as initiation codon and/or location of the uORFs may be acting to fine tune translation levels in these parasites.Submitted by Verdun Juan Pablo (jverdun@fcien.edu.uy) on 2022-06-13T16:47:46Z No. of bitstreams: 2 license_rdf: 19875 bytes, checksum: 9fdbed07f52437945402c4e70fa4773e (MD5) 10.3389fgene.2020.00166.pdf: 2794563 bytes, checksum: af40bce73ba1a739e28c94626bcd8ad6 (MD5)Approved for entry into archive by Faget Cecilia (lfaget@fcien.edu.uy) on 2022-06-24T13:23:51Z (GMT) No. of bitstreams: 2 license_rdf: 19875 bytes, checksum: 9fdbed07f52437945402c4e70fa4773e (MD5) 10.3389fgene.2020.00166.pdf: 2794563 bytes, checksum: af40bce73ba1a739e28c94626bcd8ad6 (MD5)Made available in DSpace by Luna Fabiana (fabiana.luna@seciu.edu.uy) on 2022-06-24T13:24:43Z (GMT). No. of bitstreams: 2 license_rdf: 19875 bytes, checksum: 9fdbed07f52437945402c4e70fa4773e (MD5) 10.3389fgene.2020.00166.pdf: 2794563 bytes, checksum: af40bce73ba1a739e28c94626bcd8ad6 (MD5) Previous issue date: 20209 h.application/pdfenengFrontiers MediaFrontiers in Genetics, 2020, 11:166Las obras depositadas en el Repositorio se rigen por la Ordenanza de los Derechos de la Propiedad Intelectual de la Universidad de la República.(Res. Nº 91 de C.D.C. de 8/III/1994 – D.O. 7/IV/1994) y por la Ordenanza del Repositorio Abierto de la Universidad de la República (Res. 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- Universidad de la Repúblicafalse |
spellingShingle | Upstream ORFs influence translation efficiency in the parasite Trypanosoma cruzi Radío, Santiago Trypanosoma cruzi uORF 50UTR Translation efficiency Translation regulation |
status_str | publishedVersion |
title | Upstream ORFs influence translation efficiency in the parasite Trypanosoma cruzi |
title_full | Upstream ORFs influence translation efficiency in the parasite Trypanosoma cruzi |
title_fullStr | Upstream ORFs influence translation efficiency in the parasite Trypanosoma cruzi |
title_full_unstemmed | Upstream ORFs influence translation efficiency in the parasite Trypanosoma cruzi |
title_short | Upstream ORFs influence translation efficiency in the parasite Trypanosoma cruzi |
title_sort | Upstream ORFs influence translation efficiency in the parasite Trypanosoma cruzi |
topic | Trypanosoma cruzi uORF 50UTR Translation efficiency Translation regulation |
url | https://hdl.handle.net/20.500.12008/32361 |