Evidence map›Paper›PMID 29555687›Full record

ArticleMolecular & cellular proteomics : MCP2018

Proteomic Analysis of the Cell Cycle of Procylic Form

Thomas W M Crozier, Michele Tinti, Richard J Wheeler, Tony Ly, Michael A J Ferguson, Angus I Lamond

Abstract read
In one paragraph

Article in Molecular & cellular proteomics : MCP, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 24 papers.

0numbers the graph read from it
0cells of the map it votes in
24citing 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

24 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Review
  6. Article
  7. Article
  8. Article
  9. Article
  10. Cell Cycle Progression and Synchronization: An Overview.Methods in molecular biology (Clifton, N.J.) · 2022
    Review
  11. Article
  12. Review
  13. Pathogens (Basel, Switzerland) · 2021
    Article
  14. Article
  15. Article
  16. A specific basal body linker protein provides the connection function for basal body inheritance in trypanosomes.Proceedings of the National Academy of Sciences of the United States of America · 2021
    Article
  17. Article
  18. Article
  19. Review
  20. 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.

Thomas W M CrozierFrom the ‡Wellcome Centre for Anti-Infectives Research, School of Life Sciences, University of Dundee, Dundee, DD1 5EH, UK.
Michele TintiFrom the ‡Wellcome Centre for Anti-Infectives Research, School of Life Sciences, University of Dundee, Dundee, DD1 5EH, UK.
Richard J Wheeler‖Sir William Dunn School of Pathology, University of Oxford, Oxford, OX1 3RE, UK.
Tony Ly§Centre for Gene Regulation and Expression, School of Life Sciences, University of Dundee, Dundee, DD1 5EH, UK.
Michael A J FergusonFrom the ‡Wellcome Centre for Anti-Infectives Research, School of Life Sciences, University of Dundee, Dundee, DD1 5EH, UK; a.i.lamond@dundee.ac.uk m.a.j.ferguson@dundee.ac.uk.
Angus I Lamond§Centre for Gene Regulation and Expression, School of Life Sciences, University of Dundee, Dundee, DD1 5EH, UK; a.i.lamond@dundee.ac.uk m.a.j.ferguson@dundee.ac.uk.ORCID 0000-0001-6204-6045

Funding

Wellcome Trust 050662.D10Wellcome Trust 097045/B/11/ZWellcome Trust 097945/B/11/ZWellcome Trust 101842Wellcome Trust 103261/Z/13/ZWellcome Trust 108058/Z/15/ZWellcome Trust 108445/Z/15/ZWellcome Trust 203134/Z/16/Z
6 · The paper itself

Abstract

We describe a single-step centrifugal elutriation method to produce synchronous Gap1 (G1)-phase procyclic trypanosomes at a scale amenable for proteomic analysis of the cell cycle. Using ten-plex tandem mass tag (TMT) labeling and mass spectrometry (MS)-based proteomics technology, the expression levels of 5325 proteins were quantified across the cell cycle in this parasite. Of these, 384 proteins were classified as cell-cycle regulated and subdivided into nine clusters with distinct temporal regulation. These groups included many known cell cycle regulators in trypanosomes, which validates the approach. In addition, we identify 40 novel cell cycle regulated proteins that are essential for trypanosome survival and thus represent potential future drug targets for the prevention of trypanosomiasis. Through cross-comparison to the TrypTag endogenous tagging microscopy database, we were able to validate the cell-cycle regulated patterns of expression for many of the proteins of unknown function detected in our proteomic analysis. A convenient interface to access and interrogate these data is also presented, providing a useful resource for the scientific community. Data are available via ProteomeXchange with identifier PXD008741 (https://www.ebi.ac.uk/pride/archive/).

Indexed as

Cell CycleProteomicsProtozoan ProteinsTrypanosoma brucei bruceiProtozoan ProteinsCell biology*Cell cycle*Cell division*Gene Expression*Infectious diseaseMass SpectrometryMitosisMolecular biology*ParasiteprocyclicQuantificationTrypanosoma

Identifiers

PMID29555687
PMCPMC5986242

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.