Cargando…

A Novel Toxoplasma gondii Nuclear Factor TgNF3 Is a Dynamic Chromatin-Associated Component, Modulator of Nucleolar Architecture and Parasite Virulence

In Toxoplasma gondii, cis-acting elements present in promoter sequences of genes that are stage-specifically regulated have been described. However, the nuclear factors that bind to these cis-acting elements and regulate promoter activities have not been identified. In the present study, we performe...

Descripción completa

Detalles Bibliográficos
Autores principales: Olguin-Lamas, Alejandro, Madec, Edwige, Hovasse, Agnes, Werkmeister, Elisabeth, Callebaut, Isabelle, Slomianny, Christian, Delhaye, Stephane, Mouveaux, Thomas, Schaeffer-Reiss, Christine, Van Dorsselaer, Alain, Tomavo, Stanislas
Formato: Texto
Lenguaje:English
Publicado: Public Library of Science 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3068996/
https://www.ncbi.nlm.nih.gov/pubmed/21483487
http://dx.doi.org/10.1371/journal.ppat.1001328
_version_ 1782201299625836544
author Olguin-Lamas, Alejandro
Madec, Edwige
Hovasse, Agnes
Werkmeister, Elisabeth
Callebaut, Isabelle
Slomianny, Christian
Delhaye, Stephane
Mouveaux, Thomas
Schaeffer-Reiss, Christine
Van Dorsselaer, Alain
Tomavo, Stanislas
author_facet Olguin-Lamas, Alejandro
Madec, Edwige
Hovasse, Agnes
Werkmeister, Elisabeth
Callebaut, Isabelle
Slomianny, Christian
Delhaye, Stephane
Mouveaux, Thomas
Schaeffer-Reiss, Christine
Van Dorsselaer, Alain
Tomavo, Stanislas
author_sort Olguin-Lamas, Alejandro
collection PubMed
description In Toxoplasma gondii, cis-acting elements present in promoter sequences of genes that are stage-specifically regulated have been described. However, the nuclear factors that bind to these cis-acting elements and regulate promoter activities have not been identified. In the present study, we performed affinity purification, followed by proteomic analysis, to identify nuclear factors that bind to a stage-specific promoter in T. gondii. This led to the identification of several nuclear factors in T. gondii including a novel factor, designated herein as TgNF3. The N-terminal domain of TgNF3 shares similarities with the N-terminus of yeast nuclear FK506-binding protein (FKBP), known as a histone chaperone regulating gene silencing. Using anti-TgNF3 antibodies, HA-FLAG and YFP-tagged TgNF3, we show that TgNF3 is predominantly a parasite nucleolar, chromatin-associated protein that binds specifically to T. gondii gene promoters in vivo. Genome-wide analysis using chromatin immunoprecipitation followed by high-throughput sequencing (ChIP-seq) identified promoter occupancies by TgNF3. In addition, TgNF3 has a direct role in transcriptional control of genes involved in parasite metabolism, transcription and translation. The ectopic expression of TgNF3 in the tachyzoites revealed dynamic changes in the size of the nucleolus, leading to a severe attenuation of virulence in vivo. We demonstrate that TgNF3 physically interacts with H3, H4 and H2A/H2B assembled into bona fide core and nucleosome-associated histones. Furthermore, TgNF3 interacts specifically to histones in the context of stage-specific gene silencing of a promoter that lacks active epigenetic acetylated histone marks. In contrast to virulent tachyzoites, which express the majority of TgNF3 in the nucleolus, the protein is exclusively located in the cytoplasm of the avirulent bradyzoites. We propose a model where TgNF3 acts essentially to coordinate nucleolus and nuclear functions by modulating nucleosome activities during the intracellular proliferation of the virulent tachyzoites of T. gondii.
format Text
id pubmed-3068996
institution National Center for Biotechnology Information
language English
publishDate 2011
publisher Public Library of Science
record_format MEDLINE/PubMed
spelling pubmed-30689962011-04-11 A Novel Toxoplasma gondii Nuclear Factor TgNF3 Is a Dynamic Chromatin-Associated Component, Modulator of Nucleolar Architecture and Parasite Virulence Olguin-Lamas, Alejandro Madec, Edwige Hovasse, Agnes Werkmeister, Elisabeth Callebaut, Isabelle Slomianny, Christian Delhaye, Stephane Mouveaux, Thomas Schaeffer-Reiss, Christine Van Dorsselaer, Alain Tomavo, Stanislas PLoS Pathog Research Article In Toxoplasma gondii, cis-acting elements present in promoter sequences of genes that are stage-specifically regulated have been described. However, the nuclear factors that bind to these cis-acting elements and regulate promoter activities have not been identified. In the present study, we performed affinity purification, followed by proteomic analysis, to identify nuclear factors that bind to a stage-specific promoter in T. gondii. This led to the identification of several nuclear factors in T. gondii including a novel factor, designated herein as TgNF3. The N-terminal domain of TgNF3 shares similarities with the N-terminus of yeast nuclear FK506-binding protein (FKBP), known as a histone chaperone regulating gene silencing. Using anti-TgNF3 antibodies, HA-FLAG and YFP-tagged TgNF3, we show that TgNF3 is predominantly a parasite nucleolar, chromatin-associated protein that binds specifically to T. gondii gene promoters in vivo. Genome-wide analysis using chromatin immunoprecipitation followed by high-throughput sequencing (ChIP-seq) identified promoter occupancies by TgNF3. In addition, TgNF3 has a direct role in transcriptional control of genes involved in parasite metabolism, transcription and translation. The ectopic expression of TgNF3 in the tachyzoites revealed dynamic changes in the size of the nucleolus, leading to a severe attenuation of virulence in vivo. We demonstrate that TgNF3 physically interacts with H3, H4 and H2A/H2B assembled into bona fide core and nucleosome-associated histones. Furthermore, TgNF3 interacts specifically to histones in the context of stage-specific gene silencing of a promoter that lacks active epigenetic acetylated histone marks. In contrast to virulent tachyzoites, which express the majority of TgNF3 in the nucleolus, the protein is exclusively located in the cytoplasm of the avirulent bradyzoites. We propose a model where TgNF3 acts essentially to coordinate nucleolus and nuclear functions by modulating nucleosome activities during the intracellular proliferation of the virulent tachyzoites of T. gondii. Public Library of Science 2011-03-31 /pmc/articles/PMC3068996/ /pubmed/21483487 http://dx.doi.org/10.1371/journal.ppat.1001328 Text en Olguin-Lamas et al. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Olguin-Lamas, Alejandro
Madec, Edwige
Hovasse, Agnes
Werkmeister, Elisabeth
Callebaut, Isabelle
Slomianny, Christian
Delhaye, Stephane
Mouveaux, Thomas
Schaeffer-Reiss, Christine
Van Dorsselaer, Alain
Tomavo, Stanislas
A Novel Toxoplasma gondii Nuclear Factor TgNF3 Is a Dynamic Chromatin-Associated Component, Modulator of Nucleolar Architecture and Parasite Virulence
title A Novel Toxoplasma gondii Nuclear Factor TgNF3 Is a Dynamic Chromatin-Associated Component, Modulator of Nucleolar Architecture and Parasite Virulence
title_full A Novel Toxoplasma gondii Nuclear Factor TgNF3 Is a Dynamic Chromatin-Associated Component, Modulator of Nucleolar Architecture and Parasite Virulence
title_fullStr A Novel Toxoplasma gondii Nuclear Factor TgNF3 Is a Dynamic Chromatin-Associated Component, Modulator of Nucleolar Architecture and Parasite Virulence
title_full_unstemmed A Novel Toxoplasma gondii Nuclear Factor TgNF3 Is a Dynamic Chromatin-Associated Component, Modulator of Nucleolar Architecture and Parasite Virulence
title_short A Novel Toxoplasma gondii Nuclear Factor TgNF3 Is a Dynamic Chromatin-Associated Component, Modulator of Nucleolar Architecture and Parasite Virulence
title_sort novel toxoplasma gondii nuclear factor tgnf3 is a dynamic chromatin-associated component, modulator of nucleolar architecture and parasite virulence
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3068996/
https://www.ncbi.nlm.nih.gov/pubmed/21483487
http://dx.doi.org/10.1371/journal.ppat.1001328
work_keys_str_mv AT olguinlamasalejandro anoveltoxoplasmagondiinuclearfactortgnf3isadynamicchromatinassociatedcomponentmodulatorofnucleolararchitectureandparasitevirulence
AT madecedwige anoveltoxoplasmagondiinuclearfactortgnf3isadynamicchromatinassociatedcomponentmodulatorofnucleolararchitectureandparasitevirulence
AT hovasseagnes anoveltoxoplasmagondiinuclearfactortgnf3isadynamicchromatinassociatedcomponentmodulatorofnucleolararchitectureandparasitevirulence
AT werkmeisterelisabeth anoveltoxoplasmagondiinuclearfactortgnf3isadynamicchromatinassociatedcomponentmodulatorofnucleolararchitectureandparasitevirulence
AT callebautisabelle anoveltoxoplasmagondiinuclearfactortgnf3isadynamicchromatinassociatedcomponentmodulatorofnucleolararchitectureandparasitevirulence
AT slomiannychristian anoveltoxoplasmagondiinuclearfactortgnf3isadynamicchromatinassociatedcomponentmodulatorofnucleolararchitectureandparasitevirulence
AT delhayestephane anoveltoxoplasmagondiinuclearfactortgnf3isadynamicchromatinassociatedcomponentmodulatorofnucleolararchitectureandparasitevirulence
AT mouveauxthomas anoveltoxoplasmagondiinuclearfactortgnf3isadynamicchromatinassociatedcomponentmodulatorofnucleolararchitectureandparasitevirulence
AT schaefferreisschristine anoveltoxoplasmagondiinuclearfactortgnf3isadynamicchromatinassociatedcomponentmodulatorofnucleolararchitectureandparasitevirulence
AT vandorsselaeralain anoveltoxoplasmagondiinuclearfactortgnf3isadynamicchromatinassociatedcomponentmodulatorofnucleolararchitectureandparasitevirulence
AT tomavostanislas anoveltoxoplasmagondiinuclearfactortgnf3isadynamicchromatinassociatedcomponentmodulatorofnucleolararchitectureandparasitevirulence
AT olguinlamasalejandro noveltoxoplasmagondiinuclearfactortgnf3isadynamicchromatinassociatedcomponentmodulatorofnucleolararchitectureandparasitevirulence
AT madecedwige noveltoxoplasmagondiinuclearfactortgnf3isadynamicchromatinassociatedcomponentmodulatorofnucleolararchitectureandparasitevirulence
AT hovasseagnes noveltoxoplasmagondiinuclearfactortgnf3isadynamicchromatinassociatedcomponentmodulatorofnucleolararchitectureandparasitevirulence
AT werkmeisterelisabeth noveltoxoplasmagondiinuclearfactortgnf3isadynamicchromatinassociatedcomponentmodulatorofnucleolararchitectureandparasitevirulence
AT callebautisabelle noveltoxoplasmagondiinuclearfactortgnf3isadynamicchromatinassociatedcomponentmodulatorofnucleolararchitectureandparasitevirulence
AT slomiannychristian noveltoxoplasmagondiinuclearfactortgnf3isadynamicchromatinassociatedcomponentmodulatorofnucleolararchitectureandparasitevirulence
AT delhayestephane noveltoxoplasmagondiinuclearfactortgnf3isadynamicchromatinassociatedcomponentmodulatorofnucleolararchitectureandparasitevirulence
AT mouveauxthomas noveltoxoplasmagondiinuclearfactortgnf3isadynamicchromatinassociatedcomponentmodulatorofnucleolararchitectureandparasitevirulence
AT schaefferreisschristine noveltoxoplasmagondiinuclearfactortgnf3isadynamicchromatinassociatedcomponentmodulatorofnucleolararchitectureandparasitevirulence
AT vandorsselaeralain noveltoxoplasmagondiinuclearfactortgnf3isadynamicchromatinassociatedcomponentmodulatorofnucleolararchitectureandparasitevirulence
AT tomavostanislas noveltoxoplasmagondiinuclearfactortgnf3isadynamicchromatinassociatedcomponentmodulatorofnucleolararchitectureandparasitevirulence