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Toxoplasma gondii AP2XII-2 Contributes to Transcriptional Repression for Sexual Commitment

Toxoplasma gondii is a widespread protozoan parasite that has a significant impact on human and veterinary health. The parasite undergoes a complex life cycle involving multiple hosts and developmental stages. How Toxoplasma transitions between life cycle stages is poorly understood yet central to c...

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Autores principales: Srivastava, Sandeep, Holmes, Michael J., White, Michael W., Sullivan, William J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Society for Microbiology 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10117075/
https://www.ncbi.nlm.nih.gov/pubmed/36786611
http://dx.doi.org/10.1128/msphere.00606-22
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author Srivastava, Sandeep
Holmes, Michael J.
White, Michael W.
Sullivan, William J.
author_facet Srivastava, Sandeep
Holmes, Michael J.
White, Michael W.
Sullivan, William J.
author_sort Srivastava, Sandeep
collection PubMed
description Toxoplasma gondii is a widespread protozoan parasite that has a significant impact on human and veterinary health. The parasite undergoes a complex life cycle involving multiple hosts and developmental stages. How Toxoplasma transitions between life cycle stages is poorly understood yet central to controlling transmission. Of particular neglect are the factors that contribute to its sexual development, which takes place exclusively in feline intestines. While epigenetic repressors have been shown to play an important role in silencing the spurious gene expression of sexually committed parasites, the specific factors that recruit this generalized machinery to the appropriate genes remain largely unexplored. Here, we establish that a member of the AP2 transcription factor family, AP2XII-2, is targeted to genomic loci associated with sexually committed parasites along with epigenetic regulators of transcriptional silencing, HDAC3 and MORC. Despite its widespread association with gene promoters, AP2XII-2 is required for the silencing of relatively few genes. Using the CUT&Tag (cleavage under targets and tagmentation) methodology, we identify two major genes associated with sexual development downstream of AP2XII-2 control, AP2X-10 and the amino acid hydroxylase AAH1. Our findings show that AP2XII-2 is a key contributor to the gene regulatory pathways modulating Toxoplasma sexual development. IMPORTANCE Toxoplasma gondii is a parasite that undergoes its sexual stage exclusively in feline intestines, making cats a major source of transmission. A better understanding of the proteins controlling the parasite’s life cycle stage transitions is needed for the development of new therapies aimed at treating toxoplasmosis and the transmission of the infection. Genes that regulate the sexual stages need to be turned on and off at the appropriate times, activities that are mediated by specific transcription factors that recruit general machinery to silence or activate gene expression. In this study, we identify a transcription factor called AP2XII-2 as being important for the repression of a subset of sexual stage genes, including a sexual stage-specific AP2 factor (AP2X-10) and a protein (AAH1) required to construct the infectious oocysts expelled from infected cats.
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spelling pubmed-101170752023-04-21 Toxoplasma gondii AP2XII-2 Contributes to Transcriptional Repression for Sexual Commitment Srivastava, Sandeep Holmes, Michael J. White, Michael W. Sullivan, William J. mSphere Research Article Toxoplasma gondii is a widespread protozoan parasite that has a significant impact on human and veterinary health. The parasite undergoes a complex life cycle involving multiple hosts and developmental stages. How Toxoplasma transitions between life cycle stages is poorly understood yet central to controlling transmission. Of particular neglect are the factors that contribute to its sexual development, which takes place exclusively in feline intestines. While epigenetic repressors have been shown to play an important role in silencing the spurious gene expression of sexually committed parasites, the specific factors that recruit this generalized machinery to the appropriate genes remain largely unexplored. Here, we establish that a member of the AP2 transcription factor family, AP2XII-2, is targeted to genomic loci associated with sexually committed parasites along with epigenetic regulators of transcriptional silencing, HDAC3 and MORC. Despite its widespread association with gene promoters, AP2XII-2 is required for the silencing of relatively few genes. Using the CUT&Tag (cleavage under targets and tagmentation) methodology, we identify two major genes associated with sexual development downstream of AP2XII-2 control, AP2X-10 and the amino acid hydroxylase AAH1. Our findings show that AP2XII-2 is a key contributor to the gene regulatory pathways modulating Toxoplasma sexual development. IMPORTANCE Toxoplasma gondii is a parasite that undergoes its sexual stage exclusively in feline intestines, making cats a major source of transmission. A better understanding of the proteins controlling the parasite’s life cycle stage transitions is needed for the development of new therapies aimed at treating toxoplasmosis and the transmission of the infection. Genes that regulate the sexual stages need to be turned on and off at the appropriate times, activities that are mediated by specific transcription factors that recruit general machinery to silence or activate gene expression. In this study, we identify a transcription factor called AP2XII-2 as being important for the repression of a subset of sexual stage genes, including a sexual stage-specific AP2 factor (AP2X-10) and a protein (AAH1) required to construct the infectious oocysts expelled from infected cats. American Society for Microbiology 2023-02-14 /pmc/articles/PMC10117075/ /pubmed/36786611 http://dx.doi.org/10.1128/msphere.00606-22 Text en Copyright © 2023 Srivastava et al. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution 4.0 International license (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Research Article
Srivastava, Sandeep
Holmes, Michael J.
White, Michael W.
Sullivan, William J.
Toxoplasma gondii AP2XII-2 Contributes to Transcriptional Repression for Sexual Commitment
title Toxoplasma gondii AP2XII-2 Contributes to Transcriptional Repression for Sexual Commitment
title_full Toxoplasma gondii AP2XII-2 Contributes to Transcriptional Repression for Sexual Commitment
title_fullStr Toxoplasma gondii AP2XII-2 Contributes to Transcriptional Repression for Sexual Commitment
title_full_unstemmed Toxoplasma gondii AP2XII-2 Contributes to Transcriptional Repression for Sexual Commitment
title_short Toxoplasma gondii AP2XII-2 Contributes to Transcriptional Repression for Sexual Commitment
title_sort toxoplasma gondii ap2xii-2 contributes to transcriptional repression for sexual commitment
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10117075/
https://www.ncbi.nlm.nih.gov/pubmed/36786611
http://dx.doi.org/10.1128/msphere.00606-22
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