Evidence map›Paper›PMID 33912479›Full record

ReviewFrontiers in cellular and infection microbiology2021

The Modular Circuitry of Apicomplexan Cell Division Plasticity.

Marc-Jan Gubbels, Isabelle Coppens, Kourosh Zarringhalam, Manoj T Duraisingh, Klemens Engelberg

Open access · goldAbstract readReview
In one paragraph

Review in Frontiers in cellular and infection microbiology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 25 papers.

0numbers the graph read from it
0cells of the map it votes in
25citing papers in PubMed
6.2field-weighted citation impact, top 3% 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

25 citing papers in PubMed, 41 citations in OpenAlex.

  1. Article
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  5. bioRxiv : the preprint server for biology · 2025
    Article
  6. Article
  7. Article
  8. The Crk4-Cyc4 complex regulates GThe EMBO journal · 2024
    Article
  9. The molecular mechanisms driving Plasmodium cell division.Biochemical Society transactions · 2024
    Review
  10. Article
  11. Article
  12. Article
  13. Review
  14. Article
  15. Article
  16. mBio · 2023
    Article
  17. Article
  18. Article
  19. Review
  20. Review
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

5 authors at 4 institutions in 1 country.

Marc-Jan GubbelsDepartment of Biology, Boston College, Chestnut Hill, MA, United States.
Isabelle CoppensDepartment of Molecular Microbiology and Immunology, Bloomberg School of Public Health, Johns Hopkins University, Baltimore, MD, United States.
Kourosh ZarringhalamDepartment of Mathematics, University of Massachusetts Boston, Boston, MA, United States.
Manoj T DuraisinghDepartment of Immunology and Infectious Diseases, Harvard T. H. Chan School of Public Health, Boston, MA, United States.
Klemens EngelbergDepartment of Biology, Boston College, Chestnut Hill, MA, United States.
Boston College · USHarvard University · USJohns Hopkins University · USUniversity of Massachusetts Boston · US

Funding

The Toxoplasma basal complex in cell divisionR01AI152387 · NIAID · BOSTON COLLEGE · PI GUBBELS, MARC-JAN · 2020 to 2025
$2.1M
Functional analysis of epigenetic regulators of malaria blood-stage proliferation and transmissionR01AI138551 · NIAID · HARVARD SCHOOL OF PUBLIC HEALTH · PI DURAISINGH, MANOJ T · 2018 to 2022
$2.0M
Dissecting the mechanism and regulation of Toxoplasma cytokinesisR56AI110690 · NIAID · BOSTON COLLEGE · PI GUBBELS, MARC-JAN · 2015 to 2015
$484k
Role of Autophagy in Malaria Sporozoite DifferentiationR21AI117201 · NIAID · JOHNS HOPKINS UNIVERSITY · PI COPPENS, ISABELLE · 2015 to 2016
$446k
Dissecting transcriptional mechanisms underlying Toxoplasma stage transition through in vitro evolutionR21AI150090 · NIAID · BOSTON COLLEGE · PI GUBBELS, MARC-JAN, ZARRINGHALAM, KOUROSH · 2020 to 2021
$441k
Developing comparative chemical genomics and genetic validation tools for Babesia spp.R21AI153945 · NIAID · HARVARD SCHOOL OF PUBLIC HEALTH · PI DURAISINGH, MANOJ T · 2020 to 2021
$439k
Mapping the protein landscape of the Toxoplasma basal complexR21AI128136 · NIAID · BOSTON COLLEGE · PI GUBBELS, MARC-JAN · 2017 to 2018
$430k
The Toxoplasma gondii apical annuliR21AI144856 · NIAID · BOSTON COLLEGE · PI GUBBELS, MARC-JAN · 2019 to 2020
$430k
NIAID NIH HHS R01 AI138551NIAID NIH HHS R01 AI152387NIAID NIH HHS R21 AI117201NIAID NIH HHS R21 AI128136NIAID NIH HHS R21 AI144856NIAID NIH HHS R21 AI150090NIAID NIH HHS R21 AI153945NIAID NIH HHS R56 AI110690
6 · The paper itself

Abstract

The close-knit group of apicomplexan parasites displays a wide variety of cell division modes, which differ between parasites as well as between different life stages within a single parasite species. The beginning and endpoint of the asexual replication cycles is a 'zoite' harboring the defining apical organelles required for host cell invasion. However, the number of zoites produced per division round varies dramatically and can unfold in several different ways. This plasticity of the cell division cycle originates from a combination of hard-wired developmental programs modulated by environmental triggers. Although the environmental triggers and sensors differ between species and developmental stages, widely conserved secondary messengers mediate the signal transduction pathways. These environmental and genetic input integrate in division-mode specific chromosome organization and chromatin modifications that set the stage for each division mode. Cell cycle progression is conveyed by a smorgasbord of positively and negatively acting transcription factors, often acting in concert with epigenetic reader complexes, that can vary dramatically between species as well as division modes. A unique set of cell cycle regulators with spatially distinct localization patterns insert discrete check points which permit individual control and can uncouple general cell cycle progression from nuclear amplification. Clusters of expressed genes are grouped into four functional modules seen in all division modes: 1. mother cytoskeleton disassembly; 2. DNA replication and segregation (D&S); 3. karyokinesis; 4. zoite assembly. A plug-and-play strategy results in the variety of extant division modes. The timing of mother cytoskeleton disassembly is hard-wired at the species level for asexual division modes: it is either the first step, or it is the last step. In the former scenario zoite assembly occurs at the plasma membrane (external budding), and in the latter scenario zoites are assembled in the cytoplasm (internal budding). The number of times each other module is repeated can vary regardless of this first decision, and defines the modes of cell division: schizogony, binary fission, endodyogeny, endopolygeny.

Indexed as

ToxoplasmaCell CycleCell DivisionCell NucleusDNA ReplicationApicomplexabinary fissioncell cyclecell divisionendodyogenyendopolygenykaryokinesisschizogony

Identifiers

PMID33912479
PMCPMC8072463
OpenAlexW3152971184

What Socratic 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 Socratic graph.