Evidence map›Paper›PMID 38814984›Full record

ArticlePLoS pathogens2024

The Toxoplasma gondii F-Box Protein L2 Functions as a Repressor of Stage Specific Gene Expression.

Carlos G Baptista, Sarah Hosking, Elisabet Gas-Pascual, Loic Ciampossine, Steven Abel, Mohamed-Ali Hakimi, Victoria Jeffers, Karine Le Roch, Christopher M West, Ira J Blader

Abstract read
In one paragraph

Article in PLoS pathogens, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

5 citing papers in PubMed.

  1. Review
  2. Article
  3. Article
  4. Article
  5. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

10 authors.

Carlos G BaptistaDepartment of Microbiology and Immunology, University at Buffalo School of Medicine, Buffalo, New York, United States of America.
Sarah HoskingDepartment of Microbiology and Immunology, University at Buffalo School of Medicine, Buffalo, New York, United States of America.
Elisabet Gas-PascualDepartment of Biochemistry & Molecular Biology, Center for Tropical & Emerging Global Diseases, University of Georgia, Athens, Georgia United States of America.
Loic CiampossineDepartment of Molecular, Cell, and Systems Biology, University of California Riverside, Riverside, California, United States of America.
Steven AbelDepartment of Molecular, Cell, and Systems Biology, University of California Riverside, Riverside, California, United States of America.
Mohamed-Ali HakimiHost-Pathogen Interactions and Immunity to Infection, Institute for Advanced Biosciences (IAB), INSERM U1209, CNRS UMR 5309, Grenoble Alpes University, Grenoble, France.
Victoria JeffersDepartment of Molecular, Cellular and Biomedical Sciences, University of New Hampshire, Durham, New Hampshire, United States of America.
Karine Le RochDepartment of Molecular, Cell, and Systems Biology, University of California Riverside, Riverside, California, United States of America.
Christopher M WestDepartment of Biochemistry & Molecular Biology, Center for Tropical & Emerging Global Diseases, University of Georgia, Athens, Georgia United States of America.
Ira J BladerDepartment of Microbiology and Immunology, University at Buffalo School of Medicine, Buffalo, New York, United States of America.ORCID 0000-0001-7783-3818

Funding

TLR-TRIF mediated induction of GLI3 modulates innate inflammatory responsesP20GM113131 · NIGMS · UNIVERSITY OF NEW HAMPSHIRE · PI W Kelley THOMAS · 2017 to 2026
$22.8M
Defining the cell and molecular basis of Toxoplasma recrudescenceR01AI158417 · NIAID · UNIVERSITY OF CALIFORNIA RIVERSIDE · PI WHITE, MICHAEL W, WILSON, EMMA H · 2021 to 2025
$3.5M
Chromatin structure and control of gene expression in the human malaria parasiteR01AI136511 · NIAID · UNIVERSITY OF CALIFORNIA RIVERSIDE · PI LE ROCH, KARINE GAELLE · 2018 to 2022
$3.4M
The Organization and Function of the Toxoplasma Daughter Cell ScaffoldR01AI150240 · NIAID · VIRGINIA POLYTECHNIC INST AND ST UNIV · PI BLADER, IRA J, WEST, CHRISTOPHER M. · 2020 to 2024
$3.1M
Toxoplasma F-Box Protein Regulation of the ApicoplastR21AI172206 · NIAID · STATE UNIVERSITY OF NEW YORK AT BUFFALO · PI BLADER, IRA J · 2022 to 2023
$440k
NIAID NIH HHS R01 AI136511NIAID NIH HHS R01 AI150240NIAID NIH HHS R01 AI158417NIAID NIH HHS R21 AI172206NIGMS NIH HHS P20 GM113131
6 · The paper itself

Abstract

Toxoplasma gondii is a foodborne pathogen that can cause severe and life-threatening infections in fetuses and immunocompromised patients. Felids are its only definitive hosts, and a wide range of animals, including humans, serve as intermediate hosts. When the transmissible bradyzoite stage is orally ingested by felids, they transform into merozoites that expand asexually, ultimately generating millions of gametes for the parasite sexual cycle. However, bradyzoites in intermediate hosts differentiate exclusively to disease-causing tachyzoites, which rapidly disseminate throughout the host. Though tachyzoites are well-studied, the molecular mechanisms governing transitioning between developmental stages are poorly understood. Each parasite stage can be distinguished by a characteristic transcriptional signature, with one signature being repressed during the other stages. Switching between stages require substantial changes in the proteome, which is achieved in part by ubiquitination. F-box proteins mediate protein poly-ubiquitination by recruiting substrates to SKP1, Cullin-1, F-Box protein E3 ubiquitin ligase (SCF-E3) complexes. We have identified an F-box protein named Toxoplasma gondii F-Box Protein L2 (TgFBXL2), which localizes to distinct perinucleolar sites. TgFBXL2 is stably engaged in an SCF-E3 complex that is surprisingly also associated with a COP9 signalosome complex that negatively regulates SCF-E3 function. At the cellular level, TgFBXL2-depleted parasites are severely defective in centrosome replication and daughter cell development. Most remarkable, RNAseq data show that TgFBXL2 conditional depletion induces the expression of stage-specific genes including a large cohort of genes necessary for sexual commitment. Together, these data suggest that TgFBXL2 is a latent guardian of stage specific gene expression in Toxoplasma and poised to remove conflicting proteins in response to an unknown trigger of development.

Indexed as

Protozoan ProteinsToxoplasmaAnimalsF-Box ProteinsHumansLife Cycle StagesToxoplasmosisF-Box ProteinsProtozoan Proteins

Identifiers

PMID38814984
PMCPMC11166348

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.