Evidence map›Paper›PMID 35130726›Full record

ArticlemBio2021

Novel CRK-Cyclin Complex Controls Spindle Assembly Checkpoint in

Lauren M Hawkins, Anatoli V Naumov, Mrinalini Batra, Changqi Wang, Dale Chaput, Elena S Suvorova

Open access · goldAbstract read
In one paragraph

Article in mBio, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
3.4field-weighted citation impact, top 8% 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

16 citing papers in PubMed, 19 citations in OpenAlex.

  1. Article
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  3. The Centrocone Protein SMC_N1 Is Important for the Proliferation ofAnimals : an open access journal from MDPI · 2026
    Article
  4. Assessing theBio-protocol · 2026
    Article
  5. Review
  6. Article
  7. Article
  8. Article
  9. The Crk4-Cyc4 complex regulates GThe EMBO journal · 2024
    Article
  10. mBio · 2023
    Article
  11. Article
  12. Article
  13. Article
  14. Article
  15. Article
  16. 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 1 institution in 1 country.

Lauren M HawkinsDivision of Infectious Diseases, Department of Internal Medicine, Morsani College of Medicine, University of South Floridagrid.170693.a, Tampa, Florida, USA.
Anatoli V NaumovDivision of Infectious Diseases, Department of Internal Medicine, Morsani College of Medicine, University of South Floridagrid.170693.a, Tampa, Florida, USA.
Mrinalini BatraDivision of Infectious Diseases, Department of Internal Medicine, Morsani College of Medicine, University of South Floridagrid.170693.a, Tampa, Florida, USA.
Changqi WangCollege of Public Health, University of South Floridagrid.170693.a, Tampa, Florida, USA.
Dale ChaputProteomics Core, College of Arts and Sciences, University of South Floridagrid.170693.a, Tampa, Florida, USA.
Elena S SuvorovaDivision of Infectious Diseases, Department of Internal Medicine, Morsani College of Medicine, University of South Floridagrid.170693.a, Tampa, Florida, USA.ORCID 0000-0003-4482-8144
University of South Florida · US

Funding

Cyclin-mediated control of Toxoplasma developmentR01AI141467 · NIAID · UNIVERSITY OF SOUTH FLORIDA · PI SUVOROVA, ELENA · 2020 to 2024
$1.9M
Deciphering the composite S-phase in Toxoplasma gondiiR21AI178797 · NIAID · UNIVERSITY OF SOUTH FLORIDA · PI SUVOROVA, ELENA · 2023 to 2024
$413k
New reporter system for spatiotemporal visualization of Toxoplasma gondii growth and developmentR03AI155834 · NIAID · UNIVERSITY OF SOUTH FLORIDA · PI SUVOROVA, ELENA · 2021 to 2022
$150k
NIAID NIH HHS R01 AI141467NIAID NIH HHS R03 AI155834NIAID NIH HHS R21 AI178797
6 · The paper itself

Abstract

Opportunistic parasites of the Apicomplexa phylum use a variety of division modes built on two types of cell cycles that incorporate two distinctive mechanisms of mitosis: uncoupled from and coupled to parasite budding. Parasites have evolved novel factors to regulate such unique replication mechanisms that are poorly understood. Here, we have combined genetics, quantitative fluorescence microscopy, and global proteomics approaches to examine endodyogeny in Toxoplasma gondii dividing by mitosis coupled to cytokinesis. In the current study, we focus on the steps controlled by the recently described atypical Cdk-related kinase T. gondii Crk6 (TgCrk6). While inspecting protein complexes, we found that this previously orphaned TgCrk6 kinase interacts with a parasite-specific atypical cyclin, TgCyc1. We built conditional expression models and examined primary cell cycle defects caused by the lack of TgCrk6 or TgCyc1. Quantitative microscopy assays revealed that tachyzoites deficient in either TgCrk6 or the cyclin partner TgCyc1 exhibit identical mitotic defects, suggesting cooperative action of the complex components. Further examination of the mitotic structures indicated that the TgCrk6/TgCyc1 complex regulates metaphase. This novel finding confirms a functional spindle assembly checkpoint (SAC) in T. gondii. Measuring global changes in protein expression and phosphorylation, we found evidence that canonical activities of the

Indexed as

Protozoan ProteinsToxoplasmaToxoplasmosisAnimalsCell CycleCyclin-Dependent KinasesCyclinsM Phase Cell Cycle CheckpointsProtein KinasesProto-Oncogene Proteins c-crkCRK protein, protozoanCyclin-Dependent KinasesCyclinsProtein KinasesProto-Oncogene Proteins c-crkProtozoan ProteinsApicomplexaapicomplexan parasitescell cyclecyclincyclin-dependent kinaseendodyogenymitosisprotein phosphorylationspindle assembly checkpointToxoplasma gondii

Identifiers

PMID35130726
PMCPMC8822342
OpenAlexW4210889204

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.