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A post-transcriptional respiratome regulon in trypanosomes

Post-transcriptional regulons coordinate the expression of groups of genes in eukaryotic cells, yet relatively few have been characterized. Parasitic trypanosomatids are particularly good models for studies on such mechanisms because they exhibit almost exclusive polycistronic, and unregulated, tran...

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Detalles Bibliográficos
Autores principales: Trenaman, Anna, Glover, Lucy, Hutchinson, Sebastian, Horn, David
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6648352/
https://www.ncbi.nlm.nih.gov/pubmed/31127277
http://dx.doi.org/10.1093/nar/gkz455
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author Trenaman, Anna
Glover, Lucy
Hutchinson, Sebastian
Horn, David
author_facet Trenaman, Anna
Glover, Lucy
Hutchinson, Sebastian
Horn, David
author_sort Trenaman, Anna
collection PubMed
description Post-transcriptional regulons coordinate the expression of groups of genes in eukaryotic cells, yet relatively few have been characterized. Parasitic trypanosomatids are particularly good models for studies on such mechanisms because they exhibit almost exclusive polycistronic, and unregulated, transcription. Here, we identify the Trypanosoma brucei ZC3H39/40 RNA-binding proteins as regulators of the respiratome; the mitochondrial electron transport chain (complexes I–IV) and the F(o)F(1)-ATP synthase (complex V). A high-throughput RNAi screen initially implicated both ZC3H proteins in variant surface glycoprotein (VSG) gene silencing. This link was confirmed and both proteins were shown to form a cytoplasmic ZC3H39/40 complex. Transcriptome and mRNA-interactome analyses indicated that the impact on VSG silencing was indirect, while the ZC3H39/40 complex specifically bound and stabilized transcripts encoding respiratome-complexes. Quantitative proteomic analyses revealed specific positive control of >20 components from complexes I, II and V. Our findings establish a link between the mitochondrial respiratome and VSG gene silencing in bloodstream form T. brucei. They also reveal a major respiratome regulon controlled by the conserved trypanosomatid ZC3H39/40 RNA-binding proteins.
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spelling pubmed-66483522019-07-29 A post-transcriptional respiratome regulon in trypanosomes Trenaman, Anna Glover, Lucy Hutchinson, Sebastian Horn, David Nucleic Acids Res RNA and RNA-protein complexes Post-transcriptional regulons coordinate the expression of groups of genes in eukaryotic cells, yet relatively few have been characterized. Parasitic trypanosomatids are particularly good models for studies on such mechanisms because they exhibit almost exclusive polycistronic, and unregulated, transcription. Here, we identify the Trypanosoma brucei ZC3H39/40 RNA-binding proteins as regulators of the respiratome; the mitochondrial electron transport chain (complexes I–IV) and the F(o)F(1)-ATP synthase (complex V). A high-throughput RNAi screen initially implicated both ZC3H proteins in variant surface glycoprotein (VSG) gene silencing. This link was confirmed and both proteins were shown to form a cytoplasmic ZC3H39/40 complex. Transcriptome and mRNA-interactome analyses indicated that the impact on VSG silencing was indirect, while the ZC3H39/40 complex specifically bound and stabilized transcripts encoding respiratome-complexes. Quantitative proteomic analyses revealed specific positive control of >20 components from complexes I, II and V. Our findings establish a link between the mitochondrial respiratome and VSG gene silencing in bloodstream form T. brucei. They also reveal a major respiratome regulon controlled by the conserved trypanosomatid ZC3H39/40 RNA-binding proteins. Oxford University Press 2019-07-26 2019-05-25 /pmc/articles/PMC6648352/ /pubmed/31127277 http://dx.doi.org/10.1093/nar/gkz455 Text en © The Author(s) 2019. Published by Oxford University Press on behalf of Nucleic Acids Research. http://creativecommons.org/licenses/by/4.0/ 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 reuse, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle RNA and RNA-protein complexes
Trenaman, Anna
Glover, Lucy
Hutchinson, Sebastian
Horn, David
A post-transcriptional respiratome regulon in trypanosomes
title A post-transcriptional respiratome regulon in trypanosomes
title_full A post-transcriptional respiratome regulon in trypanosomes
title_fullStr A post-transcriptional respiratome regulon in trypanosomes
title_full_unstemmed A post-transcriptional respiratome regulon in trypanosomes
title_short A post-transcriptional respiratome regulon in trypanosomes
title_sort post-transcriptional respiratome regulon in trypanosomes
topic RNA and RNA-protein complexes
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6648352/
https://www.ncbi.nlm.nih.gov/pubmed/31127277
http://dx.doi.org/10.1093/nar/gkz455
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