TcAMPK: A cellular energy homeostasis hub regulator with unique characteristics in Trypanosoma cruzi
- Autores
- Sternlieb, Tamara; Schoijet, Alejandra Cecilia; Genta, Patricio; Alonso, Guillermo Daniel
- Año de publicación
- 2020
- Idioma
- inglés
- Tipo de recurso
- documento de conferencia
- Estado
- versión publicada
- Descripción
- The AMP-activated protein kinase (AMPK) is a heterotrimeric enzyme involved in maintaining energy homeostasis in response to different stresses in many organisms. During the transition between the mammalian host and the insect vector, Trypanosoma cruzi, the causative agent of Chagas disease, faces different types of environmental fluctuations, all of which prompt the parasite to remodel its metabolism to adapt, survive and differentiate into the next stages of its life cycle. Recently, it was shown that Trypanosoma brucei AMPK is involved in the differentiation from the bloodstream slender to stumpy stage and in surface protein expression changes in response to nutritional stress. This underscores the relevance of AMPK for parasite life cycle progression. We identified four genes for the AMPK subunits of T. cruzi (α1 and α2 catalytic subunits, β and γ regulatory subunits). The β and γ subunits are largely conserved in their domain structure relative to the mammalian orthologs. However, the alpha subunits show significant sequence, structure and evolutionary differences from the human counterparts. The presence of these subunits in epimastigotes was confirmed by several techniques. TcAMPKα1 over-expressing epimastigotes showed a lower growth rate in basal culture conditions compared to the control, while α2 over-expression had the opposite effect. We found there is upregulation of AMPK activity under starvation, which is prevented if glucose is present in the culture medium. Each of these subunits could complement the ?glucose dependent? phenotype of S. cerevisiae conditional mutants lacking the respective subunit of the AMPK ortholog SNF1. Starvation and Monodansylcadaverine incorporation assays with AMPKα over-expressing parasites also showed a possible role of AMPK in autophagy. Finally, we explore the pathways in which TcAMPK may be involved using in silico analysis of putative substrates. Our results open the door to the study of the AMPK signaling pathway in Trypanosoma cruzi.
Fil: Sternlieb, Tamara. Consejo Nacional de Investigaciones Científicas y Técnicas. Instituto de Investigaciones en Ingeniería Genética y Biología Molecular "Dr. Héctor N. Torres"; Argentina
Fil: Schoijet, Alejandra Cecilia. Consejo Nacional de Investigaciones Científicas y Técnicas. Instituto de Investigaciones en Ingeniería Genética y Biología Molecular "Dr. Héctor N. Torres"; Argentina
Fil: Genta, Patricio. Consejo Nacional de Investigaciones Científicas y Técnicas. Instituto de Investigaciones en Ingeniería Genética y Biología Molecular "Dr. Héctor N. Torres"; Argentina
Fil: Alonso, Guillermo Daniel. Consejo Nacional de Investigaciones Científicas y Técnicas. Instituto de Investigaciones en Ingeniería Genética y Biología Molecular "Dr. Héctor N. Torres"; Argentina
XXXII Reunión Anual de la Sociedad Argentina de Protozoología
Ciudad Autónoma de Buenos Aires
Argentina
Sociedad Argentina de Protozoología - Materia
-
TRYPANOSOMA CRUZI
AMPK
ENERGY HOMEOSTASIS - Nivel de accesibilidad
- acceso abierto
- Condiciones de uso
- https://creativecommons.org/licenses/by-nc-sa/2.5/ar/
- Repositorio
- Institución
- Consejo Nacional de Investigaciones Científicas y Técnicas
- OAI Identificador
- oai:ri.conicet.gov.ar:11336/201599
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TcAMPK: A cellular energy homeostasis hub regulator with unique characteristics in Trypanosoma cruziSternlieb, TamaraSchoijet, Alejandra CeciliaGenta, PatricioAlonso, Guillermo DanielTRYPANOSOMA CRUZIAMPKENERGY HOMEOSTASIShttps://purl.org/becyt/ford/1.6https://purl.org/becyt/ford/1The AMP-activated protein kinase (AMPK) is a heterotrimeric enzyme involved in maintaining energy homeostasis in response to different stresses in many organisms. During the transition between the mammalian host and the insect vector, Trypanosoma cruzi, the causative agent of Chagas disease, faces different types of environmental fluctuations, all of which prompt the parasite to remodel its metabolism to adapt, survive and differentiate into the next stages of its life cycle. Recently, it was shown that Trypanosoma brucei AMPK is involved in the differentiation from the bloodstream slender to stumpy stage and in surface protein expression changes in response to nutritional stress. This underscores the relevance of AMPK for parasite life cycle progression. We identified four genes for the AMPK subunits of T. cruzi (α1 and α2 catalytic subunits, β and γ regulatory subunits). The β and γ subunits are largely conserved in their domain structure relative to the mammalian orthologs. However, the alpha subunits show significant sequence, structure and evolutionary differences from the human counterparts. The presence of these subunits in epimastigotes was confirmed by several techniques. TcAMPKα1 over-expressing epimastigotes showed a lower growth rate in basal culture conditions compared to the control, while α2 over-expression had the opposite effect. We found there is upregulation of AMPK activity under starvation, which is prevented if glucose is present in the culture medium. Each of these subunits could complement the ?glucose dependent? phenotype of S. cerevisiae conditional mutants lacking the respective subunit of the AMPK ortholog SNF1. Starvation and Monodansylcadaverine incorporation assays with AMPKα over-expressing parasites also showed a possible role of AMPK in autophagy. Finally, we explore the pathways in which TcAMPK may be involved using in silico analysis of putative substrates. Our results open the door to the study of the AMPK signaling pathway in Trypanosoma cruzi.Fil: Sternlieb, Tamara. Consejo Nacional de Investigaciones Científicas y Técnicas. Instituto de Investigaciones en Ingeniería Genética y Biología Molecular "Dr. Héctor N. Torres"; ArgentinaFil: Schoijet, Alejandra Cecilia. Consejo Nacional de Investigaciones Científicas y Técnicas. Instituto de Investigaciones en Ingeniería Genética y Biología Molecular "Dr. Héctor N. Torres"; ArgentinaFil: Genta, Patricio. Consejo Nacional de Investigaciones Científicas y Técnicas. Instituto de Investigaciones en Ingeniería Genética y Biología Molecular "Dr. Héctor N. Torres"; ArgentinaFil: Alonso, Guillermo Daniel. Consejo Nacional de Investigaciones Científicas y Técnicas. Instituto de Investigaciones en Ingeniería Genética y Biología Molecular "Dr. Héctor N. Torres"; ArgentinaXXXII Reunión Anual de la Sociedad Argentina de ProtozoologíaCiudad Autónoma de Buenos AiresArgentinaSociedad Argentina de ProtozoologíaSociedad Argentina de ProtozoologíaRiarte, Adelina RosaLonghi, Silvia AndreaFrank, Fernanda María2020info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/conferenceObjectReuniónBookhttp://purl.org/coar/resource_type/c_5794info:ar-repo/semantics/documentoDeConferenciaapplication/pdfapplication/pdfapplication/pdfhttp://hdl.handle.net/11336/201599TcAMPK: A cellular energy homeostasis hub regulator with unique characteristics in Trypanosoma cruzi; XXXII Reunión Anual de la Sociedad Argentina de Protozoología; Ciudad Autónoma de Buenos Aires; Argentina; 2020; 56-56CONICET DigitalCONICETenginfo:eu-repo/semantics/altIdentifier/url/https://protozoologia.org.ar/wp-content/uploads/Libro-de-Resumenes-SAP-2020.pdfInternacionalinfo:eu-repo/semantics/openAccesshttps://creativecommons.org/licenses/by-nc-sa/2.5/ar/reponame:CONICET Digital (CONICET)instname:Consejo Nacional de Investigaciones Científicas y Técnicas2025-09-03T09:47:34Zoai:ri.conicet.gov.ar:11336/201599instacron:CONICETInstitucionalhttp://ri.conicet.gov.ar/Organismo científico-tecnológicoNo correspondehttp://ri.conicet.gov.ar/oai/requestdasensio@conicet.gov.ar; lcarlino@conicet.gov.arArgentinaNo correspondeNo correspondeNo correspondeopendoar:34982025-09-03 09:47:34.631CONICET Digital (CONICET) - Consejo Nacional de Investigaciones Científicas y Técnicasfalse |
dc.title.none.fl_str_mv |
TcAMPK: A cellular energy homeostasis hub regulator with unique characteristics in Trypanosoma cruzi |
title |
TcAMPK: A cellular energy homeostasis hub regulator with unique characteristics in Trypanosoma cruzi |
spellingShingle |
TcAMPK: A cellular energy homeostasis hub regulator with unique characteristics in Trypanosoma cruzi Sternlieb, Tamara TRYPANOSOMA CRUZI AMPK ENERGY HOMEOSTASIS |
title_short |
TcAMPK: A cellular energy homeostasis hub regulator with unique characteristics in Trypanosoma cruzi |
title_full |
TcAMPK: A cellular energy homeostasis hub regulator with unique characteristics in Trypanosoma cruzi |
title_fullStr |
TcAMPK: A cellular energy homeostasis hub regulator with unique characteristics in Trypanosoma cruzi |
title_full_unstemmed |
TcAMPK: A cellular energy homeostasis hub regulator with unique characteristics in Trypanosoma cruzi |
title_sort |
TcAMPK: A cellular energy homeostasis hub regulator with unique characteristics in Trypanosoma cruzi |
dc.creator.none.fl_str_mv |
Sternlieb, Tamara Schoijet, Alejandra Cecilia Genta, Patricio Alonso, Guillermo Daniel |
author |
Sternlieb, Tamara |
author_facet |
Sternlieb, Tamara Schoijet, Alejandra Cecilia Genta, Patricio Alonso, Guillermo Daniel |
author_role |
author |
author2 |
Schoijet, Alejandra Cecilia Genta, Patricio Alonso, Guillermo Daniel |
author2_role |
author author author |
dc.contributor.none.fl_str_mv |
Riarte, Adelina Rosa Longhi, Silvia Andrea Frank, Fernanda María |
dc.subject.none.fl_str_mv |
TRYPANOSOMA CRUZI AMPK ENERGY HOMEOSTASIS |
topic |
TRYPANOSOMA CRUZI AMPK ENERGY HOMEOSTASIS |
purl_subject.fl_str_mv |
https://purl.org/becyt/ford/1.6 https://purl.org/becyt/ford/1 |
dc.description.none.fl_txt_mv |
The AMP-activated protein kinase (AMPK) is a heterotrimeric enzyme involved in maintaining energy homeostasis in response to different stresses in many organisms. During the transition between the mammalian host and the insect vector, Trypanosoma cruzi, the causative agent of Chagas disease, faces different types of environmental fluctuations, all of which prompt the parasite to remodel its metabolism to adapt, survive and differentiate into the next stages of its life cycle. Recently, it was shown that Trypanosoma brucei AMPK is involved in the differentiation from the bloodstream slender to stumpy stage and in surface protein expression changes in response to nutritional stress. This underscores the relevance of AMPK for parasite life cycle progression. We identified four genes for the AMPK subunits of T. cruzi (α1 and α2 catalytic subunits, β and γ regulatory subunits). The β and γ subunits are largely conserved in their domain structure relative to the mammalian orthologs. However, the alpha subunits show significant sequence, structure and evolutionary differences from the human counterparts. The presence of these subunits in epimastigotes was confirmed by several techniques. TcAMPKα1 over-expressing epimastigotes showed a lower growth rate in basal culture conditions compared to the control, while α2 over-expression had the opposite effect. We found there is upregulation of AMPK activity under starvation, which is prevented if glucose is present in the culture medium. Each of these subunits could complement the ?glucose dependent? phenotype of S. cerevisiae conditional mutants lacking the respective subunit of the AMPK ortholog SNF1. Starvation and Monodansylcadaverine incorporation assays with AMPKα over-expressing parasites also showed a possible role of AMPK in autophagy. Finally, we explore the pathways in which TcAMPK may be involved using in silico analysis of putative substrates. Our results open the door to the study of the AMPK signaling pathway in Trypanosoma cruzi. Fil: Sternlieb, Tamara. Consejo Nacional de Investigaciones Científicas y Técnicas. Instituto de Investigaciones en Ingeniería Genética y Biología Molecular "Dr. Héctor N. Torres"; Argentina Fil: Schoijet, Alejandra Cecilia. Consejo Nacional de Investigaciones Científicas y Técnicas. Instituto de Investigaciones en Ingeniería Genética y Biología Molecular "Dr. Héctor N. Torres"; Argentina Fil: Genta, Patricio. Consejo Nacional de Investigaciones Científicas y Técnicas. Instituto de Investigaciones en Ingeniería Genética y Biología Molecular "Dr. Héctor N. Torres"; Argentina Fil: Alonso, Guillermo Daniel. Consejo Nacional de Investigaciones Científicas y Técnicas. Instituto de Investigaciones en Ingeniería Genética y Biología Molecular "Dr. Héctor N. Torres"; Argentina XXXII Reunión Anual de la Sociedad Argentina de Protozoología Ciudad Autónoma de Buenos Aires Argentina Sociedad Argentina de Protozoología |
description |
The AMP-activated protein kinase (AMPK) is a heterotrimeric enzyme involved in maintaining energy homeostasis in response to different stresses in many organisms. During the transition between the mammalian host and the insect vector, Trypanosoma cruzi, the causative agent of Chagas disease, faces different types of environmental fluctuations, all of which prompt the parasite to remodel its metabolism to adapt, survive and differentiate into the next stages of its life cycle. Recently, it was shown that Trypanosoma brucei AMPK is involved in the differentiation from the bloodstream slender to stumpy stage and in surface protein expression changes in response to nutritional stress. This underscores the relevance of AMPK for parasite life cycle progression. We identified four genes for the AMPK subunits of T. cruzi (α1 and α2 catalytic subunits, β and γ regulatory subunits). The β and γ subunits are largely conserved in their domain structure relative to the mammalian orthologs. However, the alpha subunits show significant sequence, structure and evolutionary differences from the human counterparts. The presence of these subunits in epimastigotes was confirmed by several techniques. TcAMPKα1 over-expressing epimastigotes showed a lower growth rate in basal culture conditions compared to the control, while α2 over-expression had the opposite effect. We found there is upregulation of AMPK activity under starvation, which is prevented if glucose is present in the culture medium. Each of these subunits could complement the ?glucose dependent? phenotype of S. cerevisiae conditional mutants lacking the respective subunit of the AMPK ortholog SNF1. Starvation and Monodansylcadaverine incorporation assays with AMPKα over-expressing parasites also showed a possible role of AMPK in autophagy. Finally, we explore the pathways in which TcAMPK may be involved using in silico analysis of putative substrates. Our results open the door to the study of the AMPK signaling pathway in Trypanosoma cruzi. |
publishDate |
2020 |
dc.date.none.fl_str_mv |
2020 |
dc.type.none.fl_str_mv |
info:eu-repo/semantics/publishedVersion info:eu-repo/semantics/conferenceObject Reunión Book http://purl.org/coar/resource_type/c_5794 info:ar-repo/semantics/documentoDeConferencia |
status_str |
publishedVersion |
format |
conferenceObject |
dc.identifier.none.fl_str_mv |
http://hdl.handle.net/11336/201599 TcAMPK: A cellular energy homeostasis hub regulator with unique characteristics in Trypanosoma cruzi; XXXII Reunión Anual de la Sociedad Argentina de Protozoología; Ciudad Autónoma de Buenos Aires; Argentina; 2020; 56-56 CONICET Digital CONICET |
url |
http://hdl.handle.net/11336/201599 |
identifier_str_mv |
TcAMPK: A cellular energy homeostasis hub regulator with unique characteristics in Trypanosoma cruzi; XXXII Reunión Anual de la Sociedad Argentina de Protozoología; Ciudad Autónoma de Buenos Aires; Argentina; 2020; 56-56 CONICET Digital CONICET |
dc.language.none.fl_str_mv |
eng |
language |
eng |
dc.relation.none.fl_str_mv |
info:eu-repo/semantics/altIdentifier/url/https://protozoologia.org.ar/wp-content/uploads/Libro-de-Resumenes-SAP-2020.pdf |
dc.rights.none.fl_str_mv |
info:eu-repo/semantics/openAccess https://creativecommons.org/licenses/by-nc-sa/2.5/ar/ |
eu_rights_str_mv |
openAccess |
rights_invalid_str_mv |
https://creativecommons.org/licenses/by-nc-sa/2.5/ar/ |
dc.format.none.fl_str_mv |
application/pdf application/pdf application/pdf |
dc.coverage.none.fl_str_mv |
Internacional |
dc.publisher.none.fl_str_mv |
Sociedad Argentina de Protozoología |
publisher.none.fl_str_mv |
Sociedad Argentina de Protozoología |
dc.source.none.fl_str_mv |
reponame:CONICET Digital (CONICET) instname:Consejo Nacional de Investigaciones Científicas y Técnicas |
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CONICET Digital (CONICET) |
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Consejo Nacional de Investigaciones Científicas y Técnicas |
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CONICET Digital (CONICET) - Consejo Nacional de Investigaciones Científicas y Técnicas |
repository.mail.fl_str_mv |
dasensio@conicet.gov.ar; lcarlino@conicet.gov.ar |
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1842268868180967424 |
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13.13397 |