Evidence map›Paper›PMID 20864447›Full record

ArticleNucleic acids research2011

Centromere-associated topoisomerase activity in bloodstream form Trypanosoma brucei.

Samson O Obado, Christopher Bot, Maria C Echeverry, Julio C Bayona, Vanina E Alvarez, Martin C Taylor, John M Kelly

Open access · goldAbstract read
In one paragraph

Article in Nucleic acids research, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
1.7field-weighted citation impact, top 16% 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

18 citing papers in PubMed, 30 citations in OpenAlex.

  1. Article
  2. ML-792 impairsFrontiers in cellular and infection microbiology · 2026
    Article
  3. Article
  4. Review
  5. Review
  6. Site-Specific Cleavage by Topoisomerase 2: A Mark of the Core Centromere.International journal of molecular sciences · 2018
    Article
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  9. Review
  10. Review
  11. 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

7 authors at 2 institutions in 3 countries.

Samson O ObadoDepartment of Infectious and Tropical Diseases, London School of Hygiene and Tropical Medicine, London WC1E 7HT, UK.
Christopher Bot
Maria C Echeverry
Julio C Bayona
Vanina E Alvarez
Martin C Taylor
John M Kelly
University of London · GBLondon School of Hygiene & Tropical Medicine · GB

Funding

Research on trypanosomatid and apicomplexan parasitesD43TW007888 · FIC · UNIVERSITY OF GEORGIA · PI DOCAMPO, ROBERTO · 2007 to 2011
$809k
Biotechnology and Biological Sciences Research Council BB/C501292/1FIC NIH HHS D43TW007888
6 · The paper itself

Abstract

Topoisomerase-II accumulates at centromeres during prometaphase, where it resolves the DNA catenations that represent the last link between sister chromatids. Previously, using approaches including etoposide-mediated topoisomerase-II cleavage, we mapped centromeric domains in trypanosomes, early branching eukaryotes in which chromosome segregation is poorly understood. Here, we show that in bloodstream form Trypanosoma brucei, RNAi-mediated depletion of topoisomerase-IIα, but not topoisomerase-IIβ, results in the abolition of centromere-localized activity and is lethal. Both phenotypes can be rescued by expression of the corresponding enzyme from T. cruzi. Therefore, processes which govern centromere-specific topoisomerase-II accumulation/activation have been functionally conserved within trypanosomes, despite the long evolutionary separation of these species and differences in centromeric DNA organization. The variable carboxyl terminal region of topoisomerase-II has a major role in regulating biological function. We therefore generated T. brucei lines expressing T. cruzi topoisomerase-II truncated at the carboxyl terminus and examined activity at centromeres after the RNAi-mediated depletion of the endogenous enzyme. A region necessary for nuclear localization was delineated to six residues. In other organisms, sumoylation of topoisomerase-II has been shown to be necessary for regulated chromosome segregation. Evidence that we present here suggests that sumoylation of the T. brucei enzyme is not required for centromere-specific cleavage activity.

Indexed as

Amino Acid SequenceAntigens, NeoplasmCentromereDNA-Binding ProteinsDNA CleavageDNA Topoisomerases, Type IIMolecular Sequence DataRNA InterferenceSumoylationTrypanosoma brucei bruceiTrypanosoma cruziAntigens, NeoplasmDNA-Binding ProteinsDNA Topoisomerases, Type II

Identifiers

PMID20864447
PMCPMC3035458
OpenAlexW2088354543

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.