Evidence map›Paper›PMID 31286583›Full record

ArticleMolecular microbiology2019

Non-equivalence in old- and new-flagellum daughter cells of a proliferative division in Trypanosoma brucei.

Movin Abeywickrema, Hana Vachova, Helen Farr, Timm Mohr, Richard J Wheeler, De-Hua Lai, Sue Vaughan, Keith Gull, Jack D Sunter, Vladimir Varga

Abstract read
In one paragraph

Article in Molecular microbiology, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
–field-weighted citation impact
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

15 citing papers in PubMed.

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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

10 authors.

Movin AbeywickremaSir William Dunn School of Pathology, University of Oxford, Oxford, OX1 3RE, UK.
Hana VachovaInstitute of Molecular Genetics of the Czech Academy of Sciences, Vídeňská 1083, Prague, 14220, Czech Republic.
Helen FarrSir William Dunn School of Pathology, University of Oxford, Oxford, OX1 3RE, UK.
Timm MohrDepartment of Biological and Medical Sciences, Oxford Brookes University, Oxford, OX3 0BP, UK.
Richard J WheelerPeter Medawar Building for Pathogen Research, Nuffield Department of Medicine, University of Oxford, Oxford, OX1 3SY, UK.
De-Hua LaiCenter for Parasitic Organisms, State Key Laboratory of Biocontrol, School of Life Sciences, Sun Yat-Sen University, Guangzhou, 510275, P.R. China.
Sue VaughanDepartment of Biological and Medical Sciences, Oxford Brookes University, Oxford, OX3 0BP, UK.
Keith GullSir William Dunn School of Pathology, University of Oxford, Oxford, OX1 3RE, UK.
Jack D SunterDepartment of Biological and Medical Sciences, Oxford Brookes University, Oxford, OX3 0BP, UK.
Vladimir VargaInstitute of Molecular Genetics of the Czech Academy of Sciences, Vídeňská 1083, Prague, 14220, Czech Republic.ORCID 0000-0002-0384-1281

Funding

BBSRC BB/M000532/1Wellcome Trust 103261/Z/13/ZWellcome Trust 104627/Z/14/ZWellcome Trust 211075/Z/18/Z
6 · The paper itself

Abstract

Differentiation of Trypanosoma brucei, a flagellated protozoan parasite, between life cycle stages typically occurs through an asymmetric cell division process, producing two morphologically distinct daughter cells. Conversely, proliferative cell divisions produce two daughter cells, which look similar but are not identical. To examine in detail differences between the daughter cells of a proliferative division of procyclic T. brucei we used the recently identified constituents of the flagella connector. These segregate asymmetrically during cytokinesis allowing the new-flagellum and the old-flagellum daughters to be distinguished. We discovered that there are distinct morphological differences between the two daughters, with the new-flagellum daughter in particular re-modelling rapidly and extensively in early G1. This re-modelling process involves an increase in cell body, flagellum and flagellum attachment zone length and is accompanied by architectural changes to the anterior cell end. The old-flagellum daughter undergoes a different G1 re-modelling, however, despite this there was no difference in G1 duration of their respective cell cycles. This work demonstrates that the two daughters of a proliferative division of T. brucei are non-equivalent and enables more refined morphological analysis of mutant phenotypes. We suggest all proliferative divisions in T. brucei and related organisms will involve non-equivalence.

Indexed as

Cell DivisionCell ProliferationCytokinesisFlagellaLife Cycle StagesProtozoan ProteinsTrypanosoma brucei bruceiProtozoan Proteins

Identifiers

PMID31286583
PMCPMC6771564

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Registered trials

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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.