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Ribosome profiling reveals translation control as a key mechanism generating differential gene expression in Trypanosoma cruzi

BACKGROUND: Due to the absence of transcription initiation regulation of protein coding genes transcribed by RNA polymerase II, posttranscriptional regulation is responsible for the majority of gene expression changes in trypanosomatids. Therefore, cataloging the abundance of mRNAs (transcriptome) a...

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Autores principales: Smircich, Pablo, Eastman, Guillermo, Bispo, Saloe, Duhagon, María Ana, Guerra-Slompo, Eloise P, Garat, Beatriz, Goldenberg, Samuel, Munroe, David J, Dallagiovanna, Bruno, Holetz, Fabiola, Sotelo-Silveira, Jose R
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4460968/
https://www.ncbi.nlm.nih.gov/pubmed/26054634
http://dx.doi.org/10.1186/s12864-015-1563-8
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author Smircich, Pablo
Eastman, Guillermo
Bispo, Saloe
Duhagon, María Ana
Guerra-Slompo, Eloise P
Garat, Beatriz
Goldenberg, Samuel
Munroe, David J
Dallagiovanna, Bruno
Holetz, Fabiola
Sotelo-Silveira, Jose R
author_facet Smircich, Pablo
Eastman, Guillermo
Bispo, Saloe
Duhagon, María Ana
Guerra-Slompo, Eloise P
Garat, Beatriz
Goldenberg, Samuel
Munroe, David J
Dallagiovanna, Bruno
Holetz, Fabiola
Sotelo-Silveira, Jose R
author_sort Smircich, Pablo
collection PubMed
description BACKGROUND: Due to the absence of transcription initiation regulation of protein coding genes transcribed by RNA polymerase II, posttranscriptional regulation is responsible for the majority of gene expression changes in trypanosomatids. Therefore, cataloging the abundance of mRNAs (transcriptome) and the level of their translation (translatome) is a key step to understand control of gene expression in these organisms. RESULTS: Here we assess the extent of regulation of the transcriptome and the translatome in the Chagas disease causing agent, Trypanosoma cruzi, in both the non-infective (epimastigote) and infective (metacyclic trypomastigote) insect’s life stages using RNA-seq and ribosome profiling. The observed steady state transcript levels support constitutive transcription and maturation implying the existence of distinctive posttranscriptional regulatory mechanisms controlling gene expression levels at those parasite stages. Meanwhile, the downregulation of a large proportion of the translatome indicates a key role of translation control in differentiation into the infective form. The previously described proteomic data correlate better with the translatomes than with the transcriptomes and translational efficiency analysis shows a wide dynamic range, reinforcing the importance of translatability as a regulatory step. Translation efficiencies for protein families like ribosomal components are diminished while translation of the transialidase virulence factors is upregulated in the quiescent infective metacyclic trypomastigote stage. CONCLUSIONS: A large subset of genes is modulated at the translation level in two different stages of Trypanosoma cruzi life cycle. Translation upregulation of virulence factors and downregulation of ribosomal proteins indicates different degrees of control operating to prepare the parasite for an infective life form. Taking together our results show that translational regulation, in addition to regulation of steady state level of mRNA, is a major factor playing a role during the parasite differentiation. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12864-015-1563-8) contains supplementary material, which is available to authorized users.
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spelling pubmed-44609682015-06-10 Ribosome profiling reveals translation control as a key mechanism generating differential gene expression in Trypanosoma cruzi Smircich, Pablo Eastman, Guillermo Bispo, Saloe Duhagon, María Ana Guerra-Slompo, Eloise P Garat, Beatriz Goldenberg, Samuel Munroe, David J Dallagiovanna, Bruno Holetz, Fabiola Sotelo-Silveira, Jose R BMC Genomics Research Article BACKGROUND: Due to the absence of transcription initiation regulation of protein coding genes transcribed by RNA polymerase II, posttranscriptional regulation is responsible for the majority of gene expression changes in trypanosomatids. Therefore, cataloging the abundance of mRNAs (transcriptome) and the level of their translation (translatome) is a key step to understand control of gene expression in these organisms. RESULTS: Here we assess the extent of regulation of the transcriptome and the translatome in the Chagas disease causing agent, Trypanosoma cruzi, in both the non-infective (epimastigote) and infective (metacyclic trypomastigote) insect’s life stages using RNA-seq and ribosome profiling. The observed steady state transcript levels support constitutive transcription and maturation implying the existence of distinctive posttranscriptional regulatory mechanisms controlling gene expression levels at those parasite stages. Meanwhile, the downregulation of a large proportion of the translatome indicates a key role of translation control in differentiation into the infective form. The previously described proteomic data correlate better with the translatomes than with the transcriptomes and translational efficiency analysis shows a wide dynamic range, reinforcing the importance of translatability as a regulatory step. Translation efficiencies for protein families like ribosomal components are diminished while translation of the transialidase virulence factors is upregulated in the quiescent infective metacyclic trypomastigote stage. CONCLUSIONS: A large subset of genes is modulated at the translation level in two different stages of Trypanosoma cruzi life cycle. Translation upregulation of virulence factors and downregulation of ribosomal proteins indicates different degrees of control operating to prepare the parasite for an infective life form. Taking together our results show that translational regulation, in addition to regulation of steady state level of mRNA, is a major factor playing a role during the parasite differentiation. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12864-015-1563-8) contains supplementary material, which is available to authorized users. BioMed Central 2015-06-09 /pmc/articles/PMC4460968/ /pubmed/26054634 http://dx.doi.org/10.1186/s12864-015-1563-8 Text en © Smircich et al. 2015 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research Article
Smircich, Pablo
Eastman, Guillermo
Bispo, Saloe
Duhagon, María Ana
Guerra-Slompo, Eloise P
Garat, Beatriz
Goldenberg, Samuel
Munroe, David J
Dallagiovanna, Bruno
Holetz, Fabiola
Sotelo-Silveira, Jose R
Ribosome profiling reveals translation control as a key mechanism generating differential gene expression in Trypanosoma cruzi
title Ribosome profiling reveals translation control as a key mechanism generating differential gene expression in Trypanosoma cruzi
title_full Ribosome profiling reveals translation control as a key mechanism generating differential gene expression in Trypanosoma cruzi
title_fullStr Ribosome profiling reveals translation control as a key mechanism generating differential gene expression in Trypanosoma cruzi
title_full_unstemmed Ribosome profiling reveals translation control as a key mechanism generating differential gene expression in Trypanosoma cruzi
title_short Ribosome profiling reveals translation control as a key mechanism generating differential gene expression in Trypanosoma cruzi
title_sort ribosome profiling reveals translation control as a key mechanism generating differential gene expression in trypanosoma cruzi
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4460968/
https://www.ncbi.nlm.nih.gov/pubmed/26054634
http://dx.doi.org/10.1186/s12864-015-1563-8
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