Evidence map›Paper›PMID 10793160›Full record

ArticleMolecular biology of the cell2000

A novel selection regime for differentiation defects demonstrates an essential role for the stumpy form in the life cycle of the African trypanosome.

M Tasker, J Wilson, M Sarkar, E Hendriks, K Matthews

Open access · greenAbstract read
In one paragraph

Article in Molecular biology of the cell, 2000. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed
3.3field-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

20 citing papers in PubMed, 37 citations in OpenAlex.

  1. Article
  2. The Occurrence of Malignancy inFrontiers in microbiology · 2021
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  11. Hydrolysis products of cAMP analogs cause transformation of Trypanosoma brucei from slender to stumpy-like forms.Proceedings of the National Academy of Sciences of the United States of America · 2006
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  18. Genetic analysis of phenotype in Trypanosoma brucei: a classical approach to potentially complex traits.Philosophical transactions of the Royal Society of London. Series B, Biological sciences · 2002
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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 1 institution in 1 country.

M TaskerSchool of Biological Sciences, University of Manchester, Manchester M13 9PT, United Kingdom.
J Wilson
M Sarkar
E Hendriks
K Matthews
University of Manchester · GB

Funding

Wellcome Trust
6 · The paper itself

Abstract

A novel selection scheme has been developed to isolate bloodstream forms of Trypanosoma brucei, which are defective in their ability to differentiate to the procyclic stage. Detailed characterization of one selected cell line (defective in differentiation clone 1 [DiD-1]) has demonstrated that these cells are indistinguishable from the wild-type population in terms of their morphology, cell cycle progression, and biochemical characteristics but are defective in their ability to initiate differentiation to the procyclic form. Although a small proportion of DiD-1 cells remain able to transform, deletion of the genes for glycophosphatidyl inositol-phospholipase C demonstrated that this enzyme was not responsible for this inefficient differentiation. However, the attenuated growth of the Delta-glycophosphatidyl inositol-phospholipase C DiD-1 cells in mice permitted the expression of stumpy characteristics in this previously monomorphic cell line, and concomitantly their ability to differentiate efficiently was restored. Our results indicate that monomorphic cells retain expression of a characteristic of the stumpy form essential for differentiation, and that this is reduced in the defective cells. This approach provides a new route to dissection of the cytological and molecular basis of life cycle progression in the African trypanosome.

Indexed as

Protozoan ProteinsSelection, GeneticAconitic AcidAfricaAnimalsBiomarkersBromodeoxyuridineCell DifferentiationDihydrolipoamide DehydrogenaseMembrane GlycoproteinsMiceMutationPhosphoenolpyruvate Carboxykinase (ATP)Trypanosoma brucei bruceiType C PhospholipasesAconitic AcidBiomarkersBromodeoxyuridineDihydrolipoamide DehydrogenaseMembrane GlycoproteinsPhosphoenolpyruvate Carboxykinase (ATP)procyclic acidic repetitive protein, TrypanosomaProtozoan ProteinsType C Phospholipases

Identifiers

PMID10793160
PMCPMC14892
OpenAlexW2166005817

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.