Evidence map›Paper›PMID 28266506›Full record

ArticleNature communications2017

α-amino trimethylation of CENP-A by NRMT is required for full recruitment of the centromere.

Kizhakke M Sathyan, Daniele Fachinetti, Daniel R Foltz

Abstract read
In one paragraph

Article in Nature communications, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 56 papers.

0numbers the graph read from it
0cells of the map it votes in
56citing papers in PubMed
–field-weighted citation impact
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

56 citing papers in PubMed.

  1. Determinants of centromeric nucleosome conformation.bioRxiv : the preprint server for biology · 2026
    Article
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  8. Impact of Protein NLife (Basel, Switzerland) · 2023
    Review
  9. Article
  10. Article
  11. Article
  12. Article
  13. Article
  14. Cell cycle control of kinetochore assembly.Nucleus (Austin, Tex.) · 2022
    Review
  15. Review
  16. Article
  17. Methyltransferases: Functions and Applications.Chembiochem : a European journal of chemical biology · 2022
    Review
  18. Article
  19. Article
  20. 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

3 authors.

Kizhakke M SathyanDepartment of Biochemistry and Molecular Genetics, University of Virginia, Charlottesville, Virginia 22908, USA.
Daniele FachinettiDepartment of Cell Biology and Cancer, Institut Curie, PSL Research University, CNRS, UMR 144, 26 rue d'Ulm, Paris 75005, France.ORCID 0000-0002-8795-6771
Daniel R FoltzDepartment of Biochemistry and Molecular Genetics, University of Virginia, Charlottesville, Virginia 22908, USA.

Funding

Tumor Environment and Metastasis (TEAM) Research ProgramP30CA060553 · NCI · NORTHWESTERN UNIVERSITY AT CHICAGO · PI Daniela E Matei · 1993 to 2026
$153.9M
Assembly and epigenetic inheritance of the human centromereR01GM111907 · NIGMS · UNIVERSITY OF VIRGINIA · PI FOLTZ, DANIEL RICHARD · 2014 to 2022
$2.8M
NCI NIH HHS P30 CA060553NIGMS NIH HHS R01 GM111907
6 · The paper itself

Abstract

Centromeres are unique chromosomal domains that control chromosome segregation, and are epigenetically specified by the presence of the CENP-A containing nucleosomes. CENP-A governs centromere function by recruiting the constitutive centromere associated network (CCAN) complex. The features of the CENP-A nucleosome necessary to distinguish centromeric chromatin from general chromatin are not completely understood. Here we show that CENP-A undergoes α-amino trimethylation by the enzyme NRMT in vivo. We show that α-amino trimethylation of the CENP-A tail contributes to cell survival. Loss of α-amino trimethylation causes a reduction in the CENP-T and CENP-I CCAN components at the centromere and leads to lagging chromosomes and spindle pole defects. The function of p53 alters the response of cells to defects associated with decreased CENP-A methylation. Altogether we show an important functional role for α-amino trimethylation of the CENP-A nucleosome in maintaining centromere function and faithful chromosomes segregation.

Indexed as

AminesAnimalsCell ProliferationCell SurvivalCentromereCentromere Protein AChromosome SegregationHCT116 CellsHeLa CellsHumansMethylationMethyltransferasesMiceSpindle ApparatusTumor Suppressor Protein p53AminesCENPA protein, humanCentromere Protein AMethyltransferasesNTMT1 protein, humanTumor Suppressor Protein p53

Identifiers

PMID28266506
PMCPMC5343448

What OpenQuestion holds

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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 OpenQuestion graph.