Evidence map›Paper›PMID 29599445›Full record

ArticleScientific reports2018

Recruitment kinetics of the homologous recombination pathway in procyclic forms of Trypanosoma brucei after ionizing radiation treatment.

Paula Andrea Marin, Marcelo Santos da Silva, Raphael Souza Pavani, Carlos Renato Machado, Maria Carolina Elias

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
2.9field-weighted citation impact, top 9% 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

14 citing papers in PubMed, 29 citations in OpenAlex.

  1. Microbiology spectrum · 2026
    Article
  2. Article
  3. Telomere maintenance in African trypanosomes.Frontiers in molecular biosciences · 2023
    Review
  4. Article
  5. DNA Double-Strand Breaks: A Double-Edged Sword for Trypanosomatids.Frontiers in cell and developmental biology · 2021
    Review
  6. Article
  7. Specific Human ATR and ATM Inhibitors Modulate Single Strand DNA Formation inFrontiers in cellular and infection microbiology · 2021
    Article
  8. Review
  9. Article
  10. ATR Kinase Is a Crucial Player Mediating the DNA Damage Response inFrontiers in cell and developmental biology · 2020
    Article
  11. Article
  12. Article
  13. Article
  14. 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

5 authors at 2 institutions in 1 country.

Paula Andrea MarinCell Cycle Laboratory (LECC) - Center of Toxins, Immune Response and Cell Signaling (CeTICS), Butantan Institute, São Paulo, São Paulo, 05503-900, Brazil.
Marcelo Santos da SilvaCell Cycle Laboratory (LECC) - Center of Toxins, Immune Response and Cell Signaling (CeTICS), Butantan Institute, São Paulo, São Paulo, 05503-900, Brazil.ORCID 0000-0003-4203-9299
Raphael Souza PavaniCell Cycle Laboratory (LECC) - Center of Toxins, Immune Response and Cell Signaling (CeTICS), Butantan Institute, São Paulo, São Paulo, 05503-900, Brazil.
Carlos Renato MachadoBiochemical and Immunology Department, Institute of Biomedical Science, ICB, Federal University of Minas Gerais (UFMG), Minas Gerais, Belo Horizonte, 31270-901, Brazil.
Maria Carolina EliasCell Cycle Laboratory (LECC) - Center of Toxins, Immune Response and Cell Signaling (CeTICS), Butantan Institute, São Paulo, São Paulo, 05503-900, Brazil. carolina.eliassabbaga@butantan.gov.br.
Instituto Butantan · BRUniversidade Federal de Minas Gerais · BR

Funding

Wellcome Trust
6 · The paper itself

Abstract

One of the most important mechanisms for repairing double-strand breaks (DSBs) in model eukaryotes is homologous recombination (HR). Although the genes involved in HR have been found in Trypanosoma brucei and studies have identified some of the proteins that participate in this HR pathway, the recruitment kinetics of the HR machinery onto DNA during DSB repair have not been clearly elucidated in this organism. Using immunofluorescence, protein DNA-bound assays, and DNA content analysis, we established the recruitment kinetics of the HR pathway in response to the DSBs generated by ionizing radiation (IR) in procyclic forms of T. brucei. These kinetics involved the phosphorylation of histone H2A and the sequential recruitment of the essential HR players Exo1, RPA, and Rad51. The process of DSB repair took approximately 5.5 hours. We found that DSBs led to a decline in the G2/M phase after IR treatment, concomitant with cell cycle arrest in the G1/S phase. This finding suggests that HR repairs DSBs faster than the other possible DSB repair processes that act during the G1/S transition. Taken together, these data suggest that the interplay between DNA damage detection and HR machinery recruitment is finely coordinated, allowing these parasites to repair DNA rapidly after DSBs during the late S/G2 proficient phases.

Indexed as

Radiation, IonizingDNA FragmentationG1 Phase Cell Cycle CheckpointsHistonesHomologous RecombinationPhosphorylationProtozoan ProteinsRecombinational DNA RepairReplication Protein AS Phase Cell Cycle CheckpointsTrypanosoma brucei bruceiHistonesProtozoan ProteinsReplication Protein A

Identifiers

PMID29599445
PMCPMC5876374
OpenAlexW2795011724

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.