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TgKDAC4: A Unique Deacetylase of Toxoplasma’s Apicoplast
Toxoplasma gondii is an obligate intracellular parasite of the phylum Apicomplexa and causes toxoplasmosis infections, a disease that affects a quarter of the world’s population and has no effective cure. Epigenetic regulation is one of the mechanisms controlling gene expression and plays an essenti...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10302316/ https://www.ncbi.nlm.nih.gov/pubmed/37375060 http://dx.doi.org/10.3390/microorganisms11061558 |
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author | Fragoso, Mariana Sayuri Ishikawa de Siqueira, Caroline Moraes Vitorino, Francisca Nathália Luna Vieira, Alexandre Zanatta Martins-Duarte, Érica Santos Faoro, Helisson da Cunha, Júlia Pinheiro Chagas Ávila, Andréa Rodrigues Nardelli, Sheila Cristina |
author_facet | Fragoso, Mariana Sayuri Ishikawa de Siqueira, Caroline Moraes Vitorino, Francisca Nathália Luna Vieira, Alexandre Zanatta Martins-Duarte, Érica Santos Faoro, Helisson da Cunha, Júlia Pinheiro Chagas Ávila, Andréa Rodrigues Nardelli, Sheila Cristina |
author_sort | Fragoso, Mariana Sayuri Ishikawa |
collection | PubMed |
description | Toxoplasma gondii is an obligate intracellular parasite of the phylum Apicomplexa and causes toxoplasmosis infections, a disease that affects a quarter of the world’s population and has no effective cure. Epigenetic regulation is one of the mechanisms controlling gene expression and plays an essential role in all organisms. Lysine deacetylases (KDACs) act as epigenetic regulators affecting gene silencing in many eukaryotes. Here, we focus on TgKDAC4, an enzyme unique to apicomplexan parasites, and a class IV KDAC, the least-studied class of deacetylases so far. This enzyme shares only a portion of the specific KDAC domain with other organisms. Phylogenetic analysis from the TgKDAC4 domain shows a putative prokaryotic origin. Surprisingly, TgKDAC4 is located in the apicoplast, making it the only KDAC found in this organelle to date. Transmission electron microscopy assays confirmed the presence of TgKDAC4 in the periphery of the apicoplast. We identified possible targets or/and partners of TgKDAC4 by immunoprecipitation assays followed by mass spectrometry analysis, including TgCPN60 and TgGAPDH2, both located at the apicoplast and containing acetylation sites. Understanding how the protein works could provide new insights into the metabolism of the apicoplast, an essential organelle for parasite survival. |
format | Online Article Text |
id | pubmed-10302316 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-103023162023-06-29 TgKDAC4: A Unique Deacetylase of Toxoplasma’s Apicoplast Fragoso, Mariana Sayuri Ishikawa de Siqueira, Caroline Moraes Vitorino, Francisca Nathália Luna Vieira, Alexandre Zanatta Martins-Duarte, Érica Santos Faoro, Helisson da Cunha, Júlia Pinheiro Chagas Ávila, Andréa Rodrigues Nardelli, Sheila Cristina Microorganisms Article Toxoplasma gondii is an obligate intracellular parasite of the phylum Apicomplexa and causes toxoplasmosis infections, a disease that affects a quarter of the world’s population and has no effective cure. Epigenetic regulation is one of the mechanisms controlling gene expression and plays an essential role in all organisms. Lysine deacetylases (KDACs) act as epigenetic regulators affecting gene silencing in many eukaryotes. Here, we focus on TgKDAC4, an enzyme unique to apicomplexan parasites, and a class IV KDAC, the least-studied class of deacetylases so far. This enzyme shares only a portion of the specific KDAC domain with other organisms. Phylogenetic analysis from the TgKDAC4 domain shows a putative prokaryotic origin. Surprisingly, TgKDAC4 is located in the apicoplast, making it the only KDAC found in this organelle to date. Transmission electron microscopy assays confirmed the presence of TgKDAC4 in the periphery of the apicoplast. We identified possible targets or/and partners of TgKDAC4 by immunoprecipitation assays followed by mass spectrometry analysis, including TgCPN60 and TgGAPDH2, both located at the apicoplast and containing acetylation sites. Understanding how the protein works could provide new insights into the metabolism of the apicoplast, an essential organelle for parasite survival. MDPI 2023-06-12 /pmc/articles/PMC10302316/ /pubmed/37375060 http://dx.doi.org/10.3390/microorganisms11061558 Text en © 2023 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Fragoso, Mariana Sayuri Ishikawa de Siqueira, Caroline Moraes Vitorino, Francisca Nathália Luna Vieira, Alexandre Zanatta Martins-Duarte, Érica Santos Faoro, Helisson da Cunha, Júlia Pinheiro Chagas Ávila, Andréa Rodrigues Nardelli, Sheila Cristina TgKDAC4: A Unique Deacetylase of Toxoplasma’s Apicoplast |
title | TgKDAC4: A Unique Deacetylase of Toxoplasma’s Apicoplast |
title_full | TgKDAC4: A Unique Deacetylase of Toxoplasma’s Apicoplast |
title_fullStr | TgKDAC4: A Unique Deacetylase of Toxoplasma’s Apicoplast |
title_full_unstemmed | TgKDAC4: A Unique Deacetylase of Toxoplasma’s Apicoplast |
title_short | TgKDAC4: A Unique Deacetylase of Toxoplasma’s Apicoplast |
title_sort | tgkdac4: a unique deacetylase of toxoplasma’s apicoplast |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10302316/ https://www.ncbi.nlm.nih.gov/pubmed/37375060 http://dx.doi.org/10.3390/microorganisms11061558 |
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