Evidence map›Paper›PMID 25331479›Full record

ArticleBMC genomics2014

Extensive stage-regulation of translation revealed by ribosome profiling of Trypanosoma brucei.

Bryan C Jensen, Gowthaman Ramasamy, Elton J R Vasconcelos, Nicholas T Ingolia, Peter J Myler, Marilyn Parsons

Abstract read
In one paragraph

Article in BMC genomics, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 82 papers.

0numbers the graph read from it
0cells of the map it votes in
82citing 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

82 citing papers in PubMed.

  1. Article
  2. Article
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  5. Article
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  8. Article
  9. Translational control byRNA (New York, N.Y.) · 2023
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  10. Refinement ofGenes · 2023
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  14. Subcellular protein localisation ofWellcome open research · 2023
    Article
  15. Review
  16. TheRNA (New York, N.Y.) · 2022
    Article
  17. Article
  18. Article
  19. Article
  20. Review

22 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

6 authors.

Bryan C Jensen
Gowthaman Ramasamy
Elton J R Vasconcelos
Nicholas T Ingolia
Peter J Myler
Marilyn ParsonsSeattle Biomedical Research Institute, 307 Westlake Ave N, Seattle, WA 98109-5219, USA. mparsons@u.washington.edu.

Funding

Ribosome profiling of Trypanosoma bruceiR21AI094129 · NIAID · SEATTLE BIOMEDICAL RESEARCH INSTITUTE · PI MYLER, PETER JOHN, PARSONS, MARILYN · 2011 to 2012
$531k
NIAID NIH HHS 1R21 AI094129NIAID NIH HHS R21 AI094129
6 · The paper itself

Abstract

backgroundTrypanosoma brucei subspecies infect humans and animals in sub-Saharan Africa. This early diverging eukaryote shows many novel features in basic biological processes, including the use of polycistronic transcription to generate all protein-coding mRNAs. Therefore we hypothesized that translational control provides a means to tune gene expression during parasite development in mammalian and fly hosts.

resultsWe used ribosome profiling to examine genome-wide protein synthesis in animal-derived slender bloodstream forms and cultured procyclic (insect midgut) forms. About one-third of all CDSs showed statistically significant regulation of protein production between the two stages. Of these, more than two-thirds showed a change in translation efficiency, but few appeared to be controlled by this alone. Ribosomal proteins were translated poorly, especially in animal-derived parasites. A disproportionate number of metabolic enzymes were up-regulated at the mRNA level in procyclic forms, as were variant surface glycoproteins in bloodstream forms. Comparison with cultured bloodstream forms from another strain revealed stage-specific changes in gene expression that transcend strain and growth conditions. Genes with upstream ORFs had lower mean translation efficiency, but no evidence was found for involvement of uORFs in stage-regulation.

conclusionsRibosome profiling revealed that differences in the production of specific proteins in T. brucei bloodstream and procyclic forms are more extensive than predicted by analysis of mRNA abundance. While in vivo and in vitro derived bloodstream forms from different strains are more similar to one another than to procyclic forms, they showed many differences at both the mRNA and protein production level.

Indexed as

Protein BiosynthesisAnimalsGene Expression ProfilingGene Expression Regulation, DevelopmentalProtozoan ProteinsRibosomal ProteinsRNA, MessengerRNA, ProtozoanTrypanosoma brucei bruceiProtozoan ProteinsRibosomal ProteinsRNA, MessengerRNA, Protozoan

Identifiers

PMID25331479
PMCPMC4210626

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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.