Evidence map›Paper›PMID 23873148›Full record

ArticleNature cell biology2013

A two-step mechanism for epigenetic specification of centromere identity and function.

Daniele Fachinetti, H Diego Folco, Yael Nechemia-Arbely, Luis P Valente, Kristen Nguyen, Alex J Wong, Quan Zhu, Andrew J Holland, Arshad Desai, Lars E T Jansen and 1 more

Erratum issuedOpen access · greenAbstract read
In one paragraph

Article in Nature cell biology, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 177 papers.

0numbers the graph read from it
0cells of the map it votes in
177citing papers in PubMed
35.1field-weighted citation impact, top 1% 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

177 citing papers in PubMed, 260 citations in OpenAlex.

  1. Structure and function of the centromere and inner kinetochore.Nature reviews. Molecular cell biology · 2026
    Review
  2. Article
  3. Dual Roads of CENP-A for Centromere Identification.BioEssays : news and reviews in molecular, cellular and developmental biology · 2026
    Review
  4. Article
  5. Article
  6. Determinants of centromeric nucleosome conformation.bioRxiv : the preprint server for biology · 2026
    Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. Sustainable integrative cell biology: CENP-C is guilty by association.Chromosome research : an international journal on the molecular, supramolecular and evolutionary aspects of chromosome biology · 2025
    Article
  13. Article
  14. The dynamic centromere.Chromosome research : an international journal on the molecular, supramolecular and evolutionary aspects of chromosome biology · 2025
    Review
  15. Article
  16. Review
  17. Article
  18. Article
  19. Review
  20. Article

117 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

11 authors at 4 institutions in 2 countries.

Daniele FachinettiLudwig Institute for Cancer Research and Department of Cellular and Molecular Medicine, University of California at San Diego, La Jolla, California 92093, USA.
H Diego Folco
Yael Nechemia-Arbely
Luis P Valente
Kristen Nguyen
Alex J Wong
Quan Zhu
Andrew J Holland
Arshad Desai
Lars E T Jansen
Don W Cleveland
Ludwig Cancer Research · USInstituto Gulbenkian de Ciência · PTUniversity of California, San Diego · USSalk Institute for Biological Studies · US

Funding

U of Calif, San Diego Neuroscience Microscopy ImagingP30NS047101 · NINDS · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI GLEESON, JOSEPH G, ZHENG, BINHAI · 2003 to 2022
$9.0M
Mammalian Centromere AssemblyR01GM074150 · NIGMS · LUDWIG INSTITUTE FOR CANCER RES LTD · PI CLEVELAND, DON W · 2006 to 2016
$3.7M
NIGMS NIH HHS GM 074150NIGMS NIH HHS R01 GM074150NINDS NIH HHS P30 NS047101
6 · The paper itself

Abstract

The basic determinant of chromosome inheritance, the centromere, is specified in many eukaryotes by an epigenetic mark. Using gene targeting in human cells and fission yeast, chromatin containing the centromere-specific histone H3 variant CENP-A is demonstrated to be the epigenetic mark that acts through a two-step mechanism to identify, maintain and propagate centromere function indefinitely. Initially, centromere position is replicated and maintained by chromatin assembled with the centromere-targeting domain (CATD) of CENP-A substituted into H3. Subsequently, nucleation of kinetochore assembly onto CATD-containing chromatin is shown to require either the amino- or carboxy-terminal tail of CENP-A for recruitment of inner kinetochore proteins, including stabilizing CENP-B binding to human centromeres or direct recruitment of CENP-C, respectively.

Indexed as

Epigenesis, GeneticAdenoviridaeAutoantigensCentromereCentromere Protein ACentromere Protein BChromatinChromosomal Proteins, Non-HistoneEpithelial CellsGenetic VectorsHistonesHumansProtein Structure, TertiaryRetinaSchizosaccharomycesSchizosaccharomyces pombe ProteinsAutoantigensCENPA protein, humanCentromere Protein ACentromere Protein Bcentromere protein CChromatinChromosomal Proteins, Non-HistoneHistonesSchizosaccharomyces pombe Proteins

Identifiers

PMID23873148
PMCPMC4418506
OpenAlexW2042967115

What OpenQuestion holds

Textmetadata
LicenceTDM
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.