Evidence map›Paper›PMID 16607017›Full record

ArticleEukaryotic cell2006

Flagellar motility contributes to cytokinesis in Trypanosoma brucei and is modulated by an evolutionarily conserved dynein regulatory system.

Katherine S Ralston, Alana G Lerner, Dennis R Diener, Kent L Hill

Open access · diamondAbstract read
In one paragraph

Article in Eukaryotic cell, 2006. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 97 papers.

0numbers the graph read from it
0cells of the map it votes in
97citing papers in PubMed
6.7field-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

97 citing papers in PubMed, 172 citations in OpenAlex.

  1. Review
  2. Virulence · 2025
    Article
  3. CryoEM structure of thebioRxiv : the preprint server for biology · 2025
    Article
  4. Modelling motility of Trypanosoma brucei.PLoS computational biology · 2025
    Article
  5. Article
  6. FAP20 is required for flagellum assembly inMolecular biology of the cell · 2024
    Article
  7. Article
  8. Synthesis and Anti-Molecules (Basel, Switzerland) · 2024
    Article
  9. Article
  10. FAP20 is required for flagellum assembly inbioRxiv : the preprint server for biology · 2024
    Article
  11. Article
  12. FAZ assembly in bloodstream formMolecular biology of the cell · 2023
    Article
  13. Article
  14. Article
  15. Article
  16. Article
  17. Review
  18. PCD Genes-From Patients to Model Organisms and Back to Humans.International journal of molecular sciences · 2022
    Review
  19. Article
  20. Article

37 more citing papers are in PubMed but not listed here.

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

4 authors at 2 institutions in 1 country.

Katherine S RalstonDepartment of Microbiology, Immunology and Molecular Genetics, University of California, Los Angeles, 609 Charles E. Young Dr., Los Angeles, CA 90095, USA.
Alana G Lerner
Dennis R Diener
Kent L Hill
University of California, Los Angeles · USYale University · US

Funding

MARC U*STAR Program at the University of California, Los AngelesT34GM008563 · NIGMS · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI MCEVOY, MEGAN M, POE, GINA R · 1996 to 2023
$9.7M
Biochemical and Functional Analysis of TrypaninR01AI052348 · NIAID · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI HILL, KENT L · 2002 to 2023
$7.4M
PREDOCTORAL TRAINING PROGRAM IN GENETIC MECHANISMS AT UCT32GM007104 · NIGMS · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI GOBER, JAMES W · 1985 to 2011
$3.6M
NIAID NIH HHS R01 AI052348NIAID NIH HHS R01AI52348NIGMS NIH HHS GM07104NIGMS NIH HHS GM08563NIGMS NIH HHS T32 GM007104NIGMS NIH HHS T34 GM008563NINDS NIH HHS NS-0148-03
6 · The paper itself

Abstract

The flagellum of Trypanosoma brucei is a multifunctional organelle with critical roles in motility and other aspects of the trypanosome life cycle. Trypanin is a flagellar protein required for directional cell motility, but its molecular function is unknown. Recently, a trypanin homologue in Chlamydomonas reinhardtii was reported to be part of a dynein regulatory complex (DRC) that transmits regulatory signals from central pair microtubules and radial spokes to axonemal dynein. DRC genes were identified as extragenic suppressors of central pair and/or radial spoke mutations. We used RNA interference to ablate expression of radial spoke (RSP3) and central pair (PF16) components individually or in combination with trypanin. Both rsp3 and pf16 single knockdown mutants are immotile, with severely defective flagellar beat. In the case of rsp3, this loss of motility is correlated with the loss of radial spokes, while in the case of pf16 the loss of motility correlates with an aberrant orientation of the central pair microtubules within the axoneme. Genetic interaction between trypanin and PF16 is demonstrated by the finding that loss of trypanin suppresses the pf16 beat defect, indicating that the DRC represents an evolutionarily conserved strategy for dynein regulation. Surprisingly, we discovered that four independent mutants with an impaired flagellar beat all fail in the final stage of cytokinesis, indicating that flagellar motility is necessary for normal cell division in T. brucei. These findings present the first evidence that flagellar beating is important for cell division and open the opportunity to exploit enzymatic activities that drive flagellar beat as drug targets for the treatment of African sleeping sickness.

Indexed as

Conserved SequenceAmino Acid SequenceAnimalsCell MovementCytokinesisDyneinsEvolution, MolecularFlagellaMolecular Sequence DataMutationProtozoan ProteinsSequence AlignmentTrypanosoma brucei bruceiDyneinsProtozoan ProteinsT lymphocyte triggering factor, Trypanosoma brucei

Identifiers

PMID16607017
PMCPMC1459671
OpenAlexW2101070228

What OpenQuestion holds

Textmetadata
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.