Evidence map›Paper›PMID 24743791›Full record

ArticlePLoS pathogens2014

The apical complex provides a regulated gateway for secretion of invasion factors in Toxoplasma.

Nicholas J Katris, Giel G van Dooren, Paul J McMillan, Eric Hanssen, Leann Tilley, Ross F Waller

Open access · goldAbstract read
In one paragraph

Article in PLoS pathogens, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 60 papers.

0numbers the graph read from it
0cells of the map it votes in
60citing papers in PubMed
4.7field-weighted citation impact, top 4% of its field
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

60 citing papers in PubMed, 122 citations in OpenAlex.

  1. Article
  2. Article
  3. Two anchoring proteins control daughter apical complex assembly inbioRxiv : the preprint server for biology · 2026
    Article
  4. The essential function of the apical polar ring during the blood stage ofbioRxiv : the preprint server for biology · 2026
    Article
  5. Article
  6. Article
  7. Article
  8. Review
  9. Article
  10. Architecture of theProceedings of the National Academy of Sciences of the United States of America · 2024
    Article
  11. Article
  12. Article
  13. Co-dependent formation of thebioRxiv : the preprint server for biology · 2024
    Article
  14. Review
  15. Article
  16. Article
  17. Article
  18. mBio · 2023
    Article
  19. Article
  20. 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

6 authors at 3 institutions in 2 countries.

Nicholas J KatrisSchool of Botany, The University of Melbourne, Parkville, Victoria, Australia.
Giel G van DoorenResearch School of Biology, Australian National University, Canberra, Australian Capital Territory, Australia.
Paul J McMillanBiological Optical Microscopy Platform, The University of Melbourne, Parkville, Victoria, Australia.
Eric HanssenAdvanced Microscopy Facility, The University of Melbourne, Parkville, Victoria, Australia.
Leann TilleyDepartment of Biochemistry and Molecular Biology, Bio21 Molecular Science and Biotechnology Institute, and Australian Research Council Centre of Excellence for Coherent X-ray Science, The University of Melbourne, Parkville, Victoria, Australia.
Ross F WallerSchool of Botany, The University of Melbourne, Parkville, Victoria, Australia; Department of Biochemistry, University of Cambridge, Cambridge, United Kingdom.
University of Melbourne · AUAustralian National University · AUAustralian Research Council · AU

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The apical complex is the definitive cell structure of phylum Apicomplexa, and is the focus of the events of host cell penetration and the establishment of intracellular parasitism. Despite the importance of this structure, its molecular composition is relatively poorly known and few studies have experimentally tested its functions. We have characterized a novel Toxoplasma gondii protein, RNG2, that is located at the apical polar ring--the common structural element of apical complexes. During cell division, RNG2 is first recruited to centrosomes immediately after their duplication, confirming that assembly of the new apical complex commences as one of the earliest events of cell replication. RNG2 subsequently forms a ring, with the carboxy- and amino-termini anchored to the apical polar ring and mobile conoid, respectively, linking these two structures. Super-resolution microscopy resolves these two termini, and reveals that RNG2 orientation flips during invasion when the conoid is extruded. Inducible knockdown of RNG2 strongly inhibits host cell invasion. Consistent with this, secretion of micronemes is prevented in the absence of RNG2. This block, however, can be fully or partially overcome by exogenous stimulation of calcium or cGMP signaling pathways, respectively, implicating the apical complex directly in these signaling events. RNG2 demonstrates for the first time a role for the apical complex in controlling secretion of invasion factors in this important group of parasites.

Indexed as

Cell LineCyclic GMPGene Knockdown TechniquesHumansProtozoan ProteinsSignal TransductionToxoplasmaToxoplasmosisCyclic GMPProtozoan Proteins

Identifiers

PMID24743791
PMCPMC3990729
OpenAlexW2067478958

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.