Evidence map›Paper›PMID 21073906›Full record

ArticleMolecular and biochemical parasitology2011

Trypanosoma cruzi MSH2: Functional analyses on different parasite strains provide evidences for a role on the oxidative stress response.

Priscila C Campos, Viviane G Silva, Carolina Furtado, Alice Machado-Silva, Wanderson D Darocha, Eduardo F Peloso, Fernanda R Gadelha, Marisa H G Medeiros, Gustavo de Carvalho Lana, Ying Chen and 5 more

Open access · hybridAbstract read
In one paragraph

Article in Molecular and biochemical parasitology, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
2.1field-weighted citation impact, top 13% 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

19 citing papers in PubMed, 32 citations in OpenAlex.

  1. Alpha-Tubulin Acetylation inFrontiers in cellular and infection microbiology · 2021
    Article
  2. Review
  3. Frontiers in cellular and infection microbiology · 2020
    Article
  4. Article
  5. Article
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  7. Article
  8. Review
  9. Article
  10. Article
  11. Review
  12. DNA repair pathways in trypanosomatids: from DNA repair to drug resistance.Microbiology and molecular biology reviews : MMBR · 2014
    Review
  13. Article
  14. Article
  15. Article
  16. Review
  17. Article
  18. Article
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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

15 authors at 5 institutions in 2 countries.

Priscila C CamposDepartamento de Bioquímica e Imunologia, Instituto de Ciências Biológicas, Universidade Federal de Minas Gerais, Belo Horizonte, MG, Brazil.
Viviane G Silva
Carolina Furtado
Alice Machado-Silva
Wanderson D Darocha
Eduardo F Peloso
Fernanda R Gadelha
Marisa H G Medeiros
Gustavo de Carvalho Lana
Ying Chen
Rebecca L Barnes
Danielle Gomes Passos-Silva
Richard McCulloch
Carlos Renato Machado
Santuza M R Teixeira
Universidade Federal de Minas Gerais · BRUniversidade Estadual de Campinas (UNICAMP) · BRUniversity of Glasgow · GBUniversidade de São Paulo · BRWellcome Centre for Molecular Parasitology · GB

Funding

Medical Research Council G0401553Wellcome Trust
6 · The paper itself

Abstract

Components of the DNA mismatch repair (MMR) pathway are major players in processes known to generate genetic diversity, such as mutagenesis and DNA recombination. Trypanosoma cruzi, the protozoan parasite that causes Chagas disease has a highly heterogeneous population, composed of a pool of strains with distinct characteristics. Studies with a number of molecular markers identified up to six groups in the T. cruzi population, which showed distinct levels of genetic variability. To investigate the molecular basis for such differences, we analyzed the T. cruzi MSH2 gene, which encodes a key component of MMR, and showed the existence of distinct isoforms of this protein. Here we compared cell survival rates after exposure to genotoxic agents and levels of oxidative stress-induced DNA in different parasite strains. Analyses of msh2 mutants in both T. cruzi and T. brucei were also used to investigate the role of Tcmsh2 in the response to various DNA damaging agents. The results suggest that the distinct MSH2 isoforms have differences in their activity. More importantly, they also indicate that, in addition to its role in MMR, TcMSH2 acts in the parasite response to oxidative stress through a novel mitochondrial function that may be conserved in T. brucei.

Indexed as

Oxidative StressAdenosine TriphosphatasesCisplatinCross-Linking ReagentsDNA DamageDNA Mismatch RepairDNA, MitochondrialGene Expression RegulationGene Knockout TechniquesHydrogen PeroxideMolecular Sequence DataMutationMutS Homolog 2 ProteinOxidantsProtozoan ProteinsTrypanosoma brucei bruceiAdenosine TriphosphatasesCisplatinCross-Linking ReagentsDNA, MitochondrialHydrogen PeroxideMSH2 protein, Trypanosoma cruziMutS Homolog 2 ProteinOxidantsProtozoan Proteins

Identifiers

PMID21073906
PMCPMC3142612
OpenAlexW2168415069

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.