Evidence map›Paper›PMID 34737385›Full record

ArticleScientific reports2021

Metacyclogenesis defects and gene expression hallmarks of histone deacetylase 4-deficient Trypanosoma cruzi cells.

Gisele Fernanda Assine Picchi-Constante, Eloise Pavão Guerra-Slompo, Ana Carolina Tahira, Monica Visnieski Alcantara, Murilo Sena Amaral, Arthur Schveitzer Ferreira, Michel Batista, Cassiano Martin Batista, Samuel Goldenberg, Sergio Verjovski-Almeida and 1 more

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.6field-weighted citation impact, top 31% 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

2 citing papers in PubMed, 9 citations in OpenAlex.

  1. Review
  2. 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

11 authors at 3 institutions in 1 country.

Gisele Fernanda Assine Picchi-Constante *Instituto Carlos Chagas, Fiocruz Paraná, Curitiba, Paraná, 81350-010, Brazil.
Eloise Pavão Guerra-Slompo *Instituto Carlos Chagas, Fiocruz Paraná, Curitiba, Paraná, 81350-010, Brazil.
Ana Carolina TahiraLaboratório de Parasitologia, Instituto Butantan, São Paulo, SP, 05503-900, Brazil.
Monica Visnieski AlcantaraInstituto Carlos Chagas, Fiocruz Paraná, Curitiba, Paraná, 81350-010, Brazil.
Murilo Sena AmaralLaboratório de Parasitologia, Instituto Butantan, São Paulo, SP, 05503-900, Brazil.
Arthur Schveitzer FerreiraInstituto Carlos Chagas, Fiocruz Paraná, Curitiba, Paraná, 81350-010, Brazil.
Michel BatistaInstituto Carlos Chagas, Fiocruz Paraná, Curitiba, Paraná, 81350-010, Brazil.
Cassiano Martin BatistaInstituto Carlos Chagas, Fiocruz Paraná, Curitiba, Paraná, 81350-010, Brazil.
Samuel GoldenbergInstituto Carlos Chagas, Fiocruz Paraná, Curitiba, Paraná, 81350-010, Brazil.
Sergio Verjovski-AlmeidaLaboratório de Parasitologia, Instituto Butantan, São Paulo, SP, 05503-900, Brazil.
Nilson Ivo Tonin ZanchinInstituto Carlos Chagas, Fiocruz Paraná, Curitiba, Paraná, 81350-010, Brazil. nilson.zanchin@fiocruz.br.
Fundação Carlos Chagas · BRInstituto Butantan · BRUniversidade de São Paulo · BR

Funding

Conselho Nacional de Desenvolvimento Científico e Tecnológico 304167/2019-3Conselho Nacional de Desenvolvimento Científico e Tecnológico 306646/2019-6Conselho Nacional de Desenvolvimento Científico e Tecnológico 306709/2016-3Research Foundation from the state of Paraná (FapPR) 41/2018Seventh Framework Programme of the European Commission EC-GA 602080
6 · The paper itself

Abstract

Trypanosoma cruzi-the causative agent of Chagas disease-like other kinetoplastids, relies mostly on post-transcriptional mechanisms for regulation of gene expression. However, trypanosomatids undergo drastic changes in nuclear architecture and chromatin structure along their complex life cycle which, combined with a remarkable set of reversible histone post-translational modifications, indicate that chromatin is also a target for control of gene expression and differentiation signals in these organisms. Chromatin-modifying enzymes have a direct impact on gene expression programs and DNA metabolism. In this work, we have investigated the function of T. cruzi histone deacetylase 4 (TcHDAC4). We show that, although TcHDAC4 is not essential for viability, metacyclic trypomastigote TcHDAC4 null mutants show a thin cell body and a round and less condensed nucleus located very close to the kinetoplast. Sixty-four acetylation sites were quantitatively evaluated, which revealed H2AT85ac, H4K10ac and H4K78ac as potential target sites of TcHDAC4. Gene expression analyses identified three chromosomes with overrepresented regions of differentially expressed genes in the TcHDAC4 knockout mutant compared with the wild type, showing clusters of either up or downregulated genes. The adjacent chromosomal location of some of these genes indicates that TcHDAC4 participates in gene expression regulation during T. cruzi differentiation.

Indexed as

AcetylationAnimalsCell Culture TechniquesChagas DiseaseChlorocebus aethiopsChromatinGene ExpressionGene Expression RegulationHistone DeacetylasesHumansLife Cycle StagesProtein Processing, Post-TranslationalProtozoan ProteinsRepressor ProteinsTrypanosoma cruziVero CellsChromatinHDAC4 protein, humanHistone DeacetylasesProtozoan ProteinsRepressor Proteins

Identifiers

PMID34737385
PMCPMC8569148
OpenAlexW3207991879

What Socratic holds

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LicenceCC BY
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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 Socratic graph.