Evidence map›Paper›PMID 22257693›Full record

ArticleBMC genomics2012

Centromere-associated repeat arrays on Trypanosoma brucei chromosomes are much more extensive than predicted.

Maria C Echeverry, Christopher Bot, Samson O Obado, Martin C Taylor, John M Kelly

Abstract read
In one paragraph

Article in BMC genomics, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

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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

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3 · Its place in the literature

Who cites it

16 citing papers in PubMed.

  1. Article
  2. Article
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  4. RAD51-mediated R-loop formation acts to repair transcription-associated DNA breaks driving antigenic variation inProceedings of the National Academy of Sciences of the United States of America · 2023
    Article
  5. Article
  6. Review
  7. Article
  8. Article
  9. Site-Specific Cleavage by Topoisomerase 2: A Mark of the Core Centromere.International journal of molecular sciences · 2018
    Article
  10. Article
  11. Review
  12. Article
  13. Article
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  15. Article
  16. Review
4 · The record

Corrections and comments

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5 · Who and what money

Authors and funding

5 authors.

Maria C EcheverryDepartment of Infectious and Tropical Diseases, London School of Hygiene and Tropical Medicine, London, UK.
Christopher Bot
Samson O Obado
Martin C Taylor
John M Kelly

Funding

Biotechnology and Biological Sciences Research Council BB/C501292/1Biotechnology and Biological Sciences Research Council C501292/1Wellcome Trust 084175
6 · The paper itself

Abstract

backgroundAfrican trypanosomes belong to a eukaryotic lineage which displays many unusual genetic features. The mechanisms of chromosome segregation in these diploid protozoan parasites are poorly understood. Centromeres in Trypanosoma brucei have been localised to chromosomal regions that contain an array of ~147 bp AT-rich tandem repeats. Initial estimates from the genome sequencing project suggested that these arrays ranged from 2 - 8 kb. In this paper, we show that the centromeric repeat regions are much more extensive.

resultsWe used a long-range restriction endonuclease mapping approach to more accurately define the sizes of the centromeric repeat arrays on the 8 T. brucei chromosomes where unambiguous assembly data were available. The results indicate that the sizes of the arrays on different chromosomes vary from 20 to 120 kb. In addition, we found instances of length heterogeneity between chromosome homologues. For example, values of 20 and 65 kb were obtained for the arrays on chromosome 1, and 50 and 75 kb for chromosome 5.

conclusionsOur results show that centromeric repeat arrays on T. brucei chromosomes are more similar in size to those of higher eukaryotes than previously suspected. This information provides a firmer framework for investigating aspects of chromosome segregation and will allow epigenetic features associated with the process to be more accurately mapped.

Indexed as

CentromereGenome, ProtozoanOligonucleotide Array Sequence AnalysisRestriction MappingTandem Repeat SequencesTrypanosoma brucei brucei

Identifiers

PMID22257693
PMCPMC3292466

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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 OpenQuestion graph.