Evidence map›Paper›PMID 17612405›Full record

ArticleBMC genomics2007

Trichostatin A effects on gene expression in the protozoan parasite Entamoeba histolytica.

Gretchen M Ehrenkaufer, Daniel J Eichinger, Upinder Singh

Open access · goldAbstract read
In one paragraph

Article in BMC genomics, 2007. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 26 papers.

0numbers the graph read from it
0cells of the map it votes in
26citing papers in PubMed
2.5field-weighted citation impact, top 10% 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

26 citing papers in PubMed, 46 citations in OpenAlex.

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  6. Advances inFrontiers in microbiology · 2019
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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

3 authors at 2 institutions in 1 country.

Gretchen M EhrenkauferDepartment of Microbiology and Immunology, Stanford University School of Medicine, Stanford, California 94305-5107, USA. gehrenk@stanford.edu
Daniel J Eichinger
Upinder Singh
Stanford University · USNew York University · US

Funding

Investigating Entamoeba histolytica Colonic PathogenesisR01AI053724 · NIAID · STANFORD UNIVERSITY · PI SINGH, UPINDER · 2003 to 2012
$3.8M
PATHWAYS REGULATING AMOEBIC CYST FORMATIONR01AI044893 · NIAID · NEW YORK UNIVERSITY SCHOOL OF MEDICINE · PI EICHINGER, DANIEL J · 2000 to 2009
$3.4M
Developing Tools to Study Encystation in Entamoeba HistolyticaR21AI068899 · NIAID · STANFORD UNIVERSITY · PI SINGH, UPINDER · 2006 to 2007
$423k
NIAID NIH HHS R01 AI044893NIAID NIH HHS R01 AI053724NIAID NIH HHS R21 AI068899
6 · The paper itself

Abstract

backgroundHistone modification regulates chromatin structure and influences gene expression associated with diverse biological functions including cellular differentiation, cancer, maintenance of genome architecture, and pathogen virulence. In Entamoeba, a deep-branching eukaryote, short chain fatty acids (SCFA) affect histone acetylation and parasite development. Additionally, a number of active histone modifying enzymes have been identified in the parasite genome. However, the overall extent of gene regulation tied to histone acetylation is not known.

resultsIn order to identify the genome-wide effects of histone acetylation in regulating E. histolytica gene expression, we used whole-genome expression profiling of parasites treated with SCFA and Trichostatin A (TSA). Despite significant changes in histone acetylation patterns, exposure of parasites to SCFA resulted in minimal transcriptional changes (11 out of 9,435 genes transcriptionally regulated). In contrast, exposure to TSA, a more specific inhibitor of histone deacetylases, significantly affected transcription of 163 genes (122 genes upregulated and 41 genes downregulated). Genes modulated by TSA were not regulated by treatment with 5-Azacytidine, an inhibitor of DNA-methyltransferase, indicating that in E. histolytica the crosstalk between DNA methylation and histone modification is not substantial. However, the set of genes regulated by TSA overlapped substantially with genes regulated during parasite development: 73/122 genes upregulated by TSA exposure were upregulated in E. histolytica cysts (p-value = 6 x 10(-53)) and 15/41 genes downregulated by TSA exposure were downregulated in E. histolytica cysts (p-value = 3 x 10(-7)).

conclusionThis work represents the first genome-wide analysis of histone acetylation and its effects on gene expression in E. histolytica. The data indicate that SCFAs, despite their ability to influence histone acetylation, have minimal effects on gene transcription in cultured parasites. In contrast, the effect of TSA on E. histolytica gene expression is more substantial and includes genes involved in the encystation pathway. These observations will allow further dissection of the effects of histone acetylation and the genetic pathways regulating stage conversion in this pathogenic parasite.

Indexed as

AnimalsButyric AcidEntamoeba histolyticaGene Expression ProfilingGene Expression RegulationGenes, ProtozoanHistonesHydroxamic AcidsOligonucleotide Array Sequence AnalysisPropionatesReverse Transcriptase Polymerase Chain ReactionSodium AcetateButyric AcidHistonesHydroxamic AcidsPropionatesSodium Acetatesodium propionatetrichostatin A

Identifiers

PMID17612405
PMCPMC1940012
OpenAlexW2162469705

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.