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Insights into the role of endonuclease V in RNA metabolism in Trypanosoma brucei

Inosine may arise in DNA as a result of oxidative deamination of adenine or misincorporation of deoxyinosine triphosphate during replication. On the other hand, the occurrence of inosine in RNA is considered a normal and essential modification induced by specific adenosine deaminases acting on mRNA...

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Autores principales: García-Caballero, Daniel, Pérez-Moreno, Guiomar, Estévez, Antonio M., Ruíz-Pérez, Luis Miguel, Vidal, Antonio E., González-Pacanowska, Dolores
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5561087/
https://www.ncbi.nlm.nih.gov/pubmed/28819113
http://dx.doi.org/10.1038/s41598-017-08910-1
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author García-Caballero, Daniel
Pérez-Moreno, Guiomar
Estévez, Antonio M.
Ruíz-Pérez, Luis Miguel
Vidal, Antonio E.
González-Pacanowska, Dolores
author_facet García-Caballero, Daniel
Pérez-Moreno, Guiomar
Estévez, Antonio M.
Ruíz-Pérez, Luis Miguel
Vidal, Antonio E.
González-Pacanowska, Dolores
author_sort García-Caballero, Daniel
collection PubMed
description Inosine may arise in DNA as a result of oxidative deamination of adenine or misincorporation of deoxyinosine triphosphate during replication. On the other hand, the occurrence of inosine in RNA is considered a normal and essential modification induced by specific adenosine deaminases acting on mRNA and tRNA. In prokaryotes, endonuclease V (EndoV) can recognize and cleave inosine-containing DNA. In contrast, mammalian EndoVs preferentially cleave inosine-containing RNA, suggesting a role in RNA metabolism for the eukaryotic members of this protein family. We have performed a biochemical characterization of EndoV from the protozoan parasite Trypanosoma brucei. In vitro, TbEndoV efficiently processes single-stranded RNA oligonucleotides with inosine, including A to I-edited tRNA-like substrates but exhibits weak activity over DNA, except when a ribonucleotide is placed 3′ to the inosine. Immunolocalization studies performed in procyclic forms indicate that TbEndoV is mainly cytosolic yet upon nutritional stress it redistributes and accumulates in stress granules colocalizing with the DEAD-box helicase TbDhh1. RNAi-mediated depletion of TbEndoV results in moderate growth defects in procyclic cells while the two EndoV alleles could be readily knocked out in bloodstream forms. Taken together, these observations suggest an important role of TbEndoV in RNA metabolism in procyclic forms of the parasite.
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spelling pubmed-55610872017-08-18 Insights into the role of endonuclease V in RNA metabolism in Trypanosoma brucei García-Caballero, Daniel Pérez-Moreno, Guiomar Estévez, Antonio M. Ruíz-Pérez, Luis Miguel Vidal, Antonio E. González-Pacanowska, Dolores Sci Rep Article Inosine may arise in DNA as a result of oxidative deamination of adenine or misincorporation of deoxyinosine triphosphate during replication. On the other hand, the occurrence of inosine in RNA is considered a normal and essential modification induced by specific adenosine deaminases acting on mRNA and tRNA. In prokaryotes, endonuclease V (EndoV) can recognize and cleave inosine-containing DNA. In contrast, mammalian EndoVs preferentially cleave inosine-containing RNA, suggesting a role in RNA metabolism for the eukaryotic members of this protein family. We have performed a biochemical characterization of EndoV from the protozoan parasite Trypanosoma brucei. In vitro, TbEndoV efficiently processes single-stranded RNA oligonucleotides with inosine, including A to I-edited tRNA-like substrates but exhibits weak activity over DNA, except when a ribonucleotide is placed 3′ to the inosine. Immunolocalization studies performed in procyclic forms indicate that TbEndoV is mainly cytosolic yet upon nutritional stress it redistributes and accumulates in stress granules colocalizing with the DEAD-box helicase TbDhh1. RNAi-mediated depletion of TbEndoV results in moderate growth defects in procyclic cells while the two EndoV alleles could be readily knocked out in bloodstream forms. Taken together, these observations suggest an important role of TbEndoV in RNA metabolism in procyclic forms of the parasite. Nature Publishing Group UK 2017-08-17 /pmc/articles/PMC5561087/ /pubmed/28819113 http://dx.doi.org/10.1038/s41598-017-08910-1 Text en © The Author(s) 2017 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
García-Caballero, Daniel
Pérez-Moreno, Guiomar
Estévez, Antonio M.
Ruíz-Pérez, Luis Miguel
Vidal, Antonio E.
González-Pacanowska, Dolores
Insights into the role of endonuclease V in RNA metabolism in Trypanosoma brucei
title Insights into the role of endonuclease V in RNA metabolism in Trypanosoma brucei
title_full Insights into the role of endonuclease V in RNA metabolism in Trypanosoma brucei
title_fullStr Insights into the role of endonuclease V in RNA metabolism in Trypanosoma brucei
title_full_unstemmed Insights into the role of endonuclease V in RNA metabolism in Trypanosoma brucei
title_short Insights into the role of endonuclease V in RNA metabolism in Trypanosoma brucei
title_sort insights into the role of endonuclease v in rna metabolism in trypanosoma brucei
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5561087/
https://www.ncbi.nlm.nih.gov/pubmed/28819113
http://dx.doi.org/10.1038/s41598-017-08910-1
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