Evidence map›Paper›PMID 40877949›Full record

ArticleParasites & vectors2025

From mitochondrial DNA arrangement to repair: a kinetoplast-associated protein with different roles in two trypanosomatid species.

Camila Silva Gonçalves, Carolina Moura Costa Catta-Preta, Bruno Marçal Repolês, Wesley Roger Rodrigues Ferreira, Flavia Souza Morini, Jeremy C Mottram, Danielle Pereira Cavalcanti, Wanderley de Souza, Stenio Perdigão Fragoso, Carlos Renato Machado and 1 more

Abstract read
In one paragraph

Article in Parasites & vectors, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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.

Camila Silva GonçalvesLaboratório de Ultraestrutura Celular Hertha Meyer, Centro de Pesquisa em Medicina de Precisão (CPMP), Instituto de Biofísica Carlos Chagas Filho, Universidade Federal Do Rio de Janeiro, Cidade Universitária, Rio de Janeiro, RJ, CEP 21941-590, Brazil.
Carolina Moura Costa Catta-PretaDepartment of Biology, York Biomedical Research Institute, University of York, Wentworth Way, Heslington, York, YO10 5DD, UK.
Bruno Marçal RepolêsDepartamento de Bioquímica e Imunologia, Laboratório de Genética Bioquímica, Instituto de Ciências Biológicas, Universidade Federal de Minas Gerais, Belo Horizonte, Brazil.
Wesley Roger Rodrigues FerreiraDepartamento de Bioquímica e Imunologia, Laboratório de Genética Bioquímica, Instituto de Ciências Biológicas, Universidade Federal de Minas Gerais, Belo Horizonte, Brazil.
Flavia Souza MoriniLaboratório de Biologia Molecular e Sistêmica de Tripanossomatídeos, Instituto Carlos Chagas, Fundação Oswaldo Cruz (FIOCRUZ), Curitiba, Brazil.
Jeremy C MottramDepartment of Biology, York Biomedical Research Institute, University of York, Wentworth Way, Heslington, York, YO10 5DD, UK.
Danielle Pereira CavalcantiLaboratório de Microbiologia, Diretoria de Metrologia Científica, Industrial e Tecnologia, Instituto Nacional de Metrologia, Qualidade e Tecnologia - Inmetro, Duque de Caxias, RJ, Brazil.
Wanderley de SouzaLaboratório de Ultraestrutura Celular Hertha Meyer, Centro de Pesquisa em Medicina de Precisão (CPMP), Instituto de Biofísica Carlos Chagas Filho, Universidade Federal Do Rio de Janeiro, Cidade Universitária, Rio de Janeiro, RJ, CEP 21941-590, Brazil.
Stenio Perdigão FragosoLaboratório de Biologia Molecular e Sistêmica de Tripanossomatídeos, Instituto Carlos Chagas, Fundação Oswaldo Cruz (FIOCRUZ), Curitiba, Brazil.
Carlos Renato MachadoDepartamento de Bioquímica e Imunologia, Laboratório de Genética Bioquímica, Instituto de Ciências Biológicas, Universidade Federal de Minas Gerais, Belo Horizonte, Brazil. crmachad@icb.ufmg.br.
Maria Cristina M MottaLaboratório de Ultraestrutura Celular Hertha Meyer, Centro de Pesquisa em Medicina de Precisão (CPMP), Instituto de Biofísica Carlos Chagas Filho, Universidade Federal Do Rio de Janeiro, Cidade Universitária, Rio de Janeiro, RJ, CEP 21941-590, Brazil. motta@biof.ufrj.br.

Funding

Conselho Nacional de Desenvolvimento Científico e Tecnológico 305299/2022-0Fundação Carlos Chagas Filho de Amparo à Pesquisa do Estado do Rio de Janeiro E-26/201.011/2021Fundação de Amparo à Pesquisa do Estado de Minas Gerais APQ-02533-24, BPD-00548-22
6 · The paper itself

Abstract

backgroundOne of the most intriguing and unusual features of trypanosomatids is their mitochondrial DNA, known as kinetoplast DNA (kDNA), which is organized into a network of concatenated circles. The kDNA is contained within the mitochondrial matrix and can exhibit distinct arrangements across different species and during cell differentiation. In addition to kDNA, the kinetoplast contains multiple proteins, including those involved in mitochondrial DNA topology and metabolism, such as the kinetoplast-associated proteins (KAPs). In this work, we obtained mutant cells to investigates the role of KAP7 in two trypanosomatid species, Trypanosoma cruzi and Angomonas deanei, which have distinct kinetoplast shapes and kDNA arrangements.

methodsFor this purpose, the kDNA replication process and cell morphology and ultrastructure were evaluated using microscopy methods. Furthermore, the proliferation of cells treated with genotoxic agents, such as cisplatin and ultraviolet radiation, was analyzed.

resultsIn A. deanei, which contains a symbiotic bacterium, KAP7 seems to be essential, since the deletion of one KAP7 allele generated mutants with a decay in cell proliferation, as well as changes in kDNA structure and replication. In T. cruzi, null mutants exhibited disturbances in kDNA replication, although the overall topology remained unaltered. The use of cisplatin and ultraviolet (UV) radiation affected the ultrastructure of A. deanei and T. cruzi. Cisplatin promoted increased kDNA compaction in both KAP7 mutants, but only in T. cruzi did the proliferative capacity fail to recover after treatment, as was also observed following UV radiation exposure.

conclusionsProteins associated with DNA are evolutionarily conserved and usually perform similar functions in different organisms. Our findings reveal that KAP7 is involved in kDNA replication, but its roles differ in trypanosomatid species: in A. deanei, KAP7 is associated with kDNA arrangement, while in T. cruzi, it is related to mitochondrial metabolism, such as kDNA replication and damage response.

Indexed as

DNA, KinetoplastDNA, MitochondrialDNA RepairProtozoan ProteinsTrypanosoma cruziTrypanosomatinaAnimalsDNA, ProtozoanDNA ReplicationMitochondriaDNA, KinetoplastDNA, MitochondrialDNA, ProtozoanProtozoan ProteinsCell proliferationGenotoxic agentskDNA replication and topologyKinetoplast-associated proteins (KAPs)SymbiosisTrypanosomatidsUltrastructure

Identifiers

PMID40877949
PMCPMC12395728

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.