Evidence map›Paper›PMID 19664227›Full record

ArticleBMC genomics2009

The steady-state transcriptome of the four major life-cycle stages of Trypanosoma cruzi.

Todd A Minning, D Brent Weatherly, James Atwood, Ron Orlando, Rick L Tarleton

Open access · goldAbstract read
In one paragraph

Article in BMC genomics, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 75 papers.

0numbers the graph read from it
0cells of the map it votes in
75citing papers in PubMed
7.2field-weighted citation impact, top 2% 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

75 citing papers in PubMed, 133 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Article
  5. Metacyclogenesis as the Starting Point of Chagas Disease.International journal of molecular sciences · 2023
    Review
  6. Article
  7. Modulation of Virulence Factors duringPathogens (Basel, Switzerland) · 2022
    Review
  8. Article
  9. Article
  10. Review
  11. Review
  12. Article
  13. Article
  14. Article
  15. Genes · 2020
    Review
  16. Article
  17. Article
  18. Article
  19. Article
  20. Frontiers in immunology · 2019
    Article

15 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

5 authors at 1 institution in 1 country.

Todd A MinningCenter for Tropical and Emerging Global Diseases, University of Georgia, Athens, Georgia 30602, USA. tminning@uga.edu
D Brent Weatherly
James Atwood
Ron Orlando
Rick L Tarleton
University of Georgia · US

Funding

VACCINE DISCOVERY FOR TRYPANOSOMA CRUZIP01AI044979 · NIAID · UNIVERSITY OF GEORGIA (UGA) · PI TARLETON, RICK L · 1999 to 2008
$7.5M
Microarray analysis of gene expresion in T. cruziR03AI064622 · NIAID · UNIVERSITY OF GEORGIA (UGA) · PI TARLETON, RICK L · 2005 to 2006
$145k
NIAID NIH HHS P01AI044979NIAID NIH HHS R03AI064622
6 · The paper itself

Abstract

backgroundChronic chagasic cardiomyopathy is a debilitating and frequently fatal outcome of human infection with the protozoan parasite, Trypanosoma cruzi. Microarray analysis of gene expression during the T. cruzi life-cycle could be a valuable means of identifying drug and vaccine targets based on their appropriate expression patterns, but results from previous microarray studies in T. cruzi and related kinetoplastid parasites have suggested that the transcript abundances of most genes in these organisms do not vary significantly between life-cycle stages.

resultsIn this study, we used whole genome, oligonucleotide microarrays to globally determine the extent to which T. cruzi regulates mRNA relative abundances over the course of its complete life-cycle. In contrast to previous microarray studies in kinetoplastids, we observed that relative transcript abundances for over 50% of the genes detected on the T. cruzi microarrays were significantly regulated during the T. cruzi life-cycle. The significant regulation of 25 of these genes was confirmed by quantitative reverse-transcriptase PCR (qRT-PCR). The T. cruzi transcriptome also mirrored published protein expression data for several functional groups. Among the differentially regulated genes were members of paralog clusters, nearly 10% of which showed divergent expression patterns between cluster members.

conclusionTaken together, these data support the conclusion that transcript abundance is an important level of gene expression regulation in T. cruzi. Thus, microarray analysis is a valuable screening tool for identifying stage-regulated T. cruzi genes and metabolic pathways.

Indexed as

Gene Expression Regulation, DevelopmentalLife Cycle StagesAnimalsGene Expression ProfilingGenome, ProtozoanOligonucleotide Array Sequence AnalysisProteomicsProtozoan ProteinsReverse Transcriptase Polymerase Chain ReactionRNA, MessengerTranscription, GeneticTrypanosoma cruziProtozoan ProteinsRNA, Messenger

Identifiers

PMID19664227
PMCPMC2907688
OpenAlexW2124769246

What OpenQuestion 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 OpenQuestion graph.