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

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...

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Veröffentlicht in:BMC genomics 2015-06, Vol.16 (1), p.443-443, Article 443
Hauptverfasser: 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
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container_title BMC genomics
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creator 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
description 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. 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. 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.
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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. 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. 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. 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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. 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. 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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><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c640t-c001e9db51349ae01829372d21fa1f5ca45a570999aba8a671cd01b3a45572f23</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2015</creationdate><topic>Analysis</topic><topic>Chagas' disease</topic><topic>Down-Regulation</topic><topic>Gene Expression Profiling - methods</topic><topic>Gene Expression Regulation, Developmental</topic><topic>Genetic aspects</topic><topic>Genetic transcription</topic><topic>Life Cycle Stages</topic><topic>Messenger RNA</topic><topic>Physiological aspects</topic><topic>Protein Processing, Post-Translational</topic><topic>Proteomics - methods</topic><topic>Protozoan Proteins - analysis</topic><topic>Ribosomes - metabolism</topic><topic>RNA, Protozoan - analysis</topic><topic>Trypanosoma cruzi - genetics</topic><topic>Trypanosoma cruzi - growth &amp; development</topic><topic>Trypanosoma cruzi - metabolism</topic><topic>Up-Regulation</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Smircich, Pablo</creatorcontrib><creatorcontrib>Eastman, Guillermo</creatorcontrib><creatorcontrib>Bispo, Saloe</creatorcontrib><creatorcontrib>Duhagon, María Ana</creatorcontrib><creatorcontrib>Guerra-Slompo, Eloise P</creatorcontrib><creatorcontrib>Garat, Beatriz</creatorcontrib><creatorcontrib>Goldenberg, Samuel</creatorcontrib><creatorcontrib>Munroe, David J</creatorcontrib><creatorcontrib>Dallagiovanna, Bruno</creatorcontrib><creatorcontrib>Holetz, Fabiola</creatorcontrib><creatorcontrib>Sotelo-Silveira, Jose R</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Gale In Context: Science</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>BMC genomics</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Smircich, Pablo</au><au>Eastman, Guillermo</au><au>Bispo, Saloe</au><au>Duhagon, María Ana</au><au>Guerra-Slompo, Eloise P</au><au>Garat, Beatriz</au><au>Goldenberg, Samuel</au><au>Munroe, David J</au><au>Dallagiovanna, Bruno</au><au>Holetz, Fabiola</au><au>Sotelo-Silveira, Jose R</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Ribosome profiling reveals translation control as a key mechanism generating differential gene expression in Trypanosoma cruzi</atitle><jtitle>BMC genomics</jtitle><addtitle>BMC Genomics</addtitle><date>2015-06-09</date><risdate>2015</risdate><volume>16</volume><issue>1</issue><spage>443</spage><epage>443</epage><pages>443-443</pages><artnum>443</artnum><issn>1471-2164</issn><eissn>1471-2164</eissn><abstract>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. 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. 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.</abstract><cop>England</cop><pub>BioMed Central Ltd</pub><pmid>26054634</pmid><doi>10.1186/s12864-015-1563-8</doi><tpages>1</tpages><oa>free_for_read</oa></addata></record>
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subjects Analysis
Chagas' disease
Down-Regulation
Gene Expression Profiling - methods
Gene Expression Regulation, Developmental
Genetic aspects
Genetic transcription
Life Cycle Stages
Messenger RNA
Physiological aspects
Protein Processing, Post-Translational
Proteomics - methods
Protozoan Proteins - analysis
Ribosomes - metabolism
RNA, Protozoan - analysis
Trypanosoma cruzi - genetics
Trypanosoma cruzi - growth & development
Trypanosoma cruzi - metabolism
Up-Regulation
title Ribosome profiling reveals translation control as a key mechanism generating differential gene expression in Trypanosoma cruzi
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