Evidence map›Paper›PMID 31160708›Full record

ArticleNature cell biology2019

DNA replication acts as an error correction mechanism to maintain centromere identity by restricting CENP-A to centromeres.

Yael Nechemia-Arbely, Karen H Miga, Ofer Shoshani, Aaron Aslanian, Moira A McMahon, Ah Young Lee, Daniele Fachinetti, John R Yates, Bing Ren, Don W Cleveland

Open access · greenAbstract read
In one paragraph

Article in Nature cell biology, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 64 papers.

0numbers the graph read from it
0cells of the map it votes in
64citing papers in PubMed
5.3field-weighted citation impact, top 3% 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

64 citing papers in PubMed, 99 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. Article
  7. Article
  8. Article
  9. Article
  10. The dynamic centromere.Chromosome research : an international journal on the molecular, supramolecular and evolutionary aspects of chromosome biology · 2025
    Review
  11. Article
  12. Preserving centromere identity: right amounts of CENP-A at the right place and time.Chromosome research : an international journal on the molecular, supramolecular and evolutionary aspects of chromosome biology · 2025
    Review
  13. A brief historical perspective on cell cycle control of CENP-A assembly and inheritance.Chromosome research : an international journal on the molecular, supramolecular and evolutionary aspects of chromosome biology · 2025
    Review
  14. Review
  15. Article
  16. Article
  17. Article
  18. DNA strand breaks at centromeres: Friend or foe?Seminars in cell & developmental biology · 2024
    Review
  19. Article
  20. Article

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

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

10 authors at 6 institutions in 3 countries.

Yael Nechemia-ArbelyLudwig Institute for Cancer Research and Department of Cellular and Molecular Medicine, University of California at San Diego, La Jolla, CA, USA. arbelyy@upmc.edu.ORCID http://orcid.org/0000-0001-5753-5485
Karen H MigaCenter for Biomolecular Science & Engineering, University of California Santa Cruz, Santa Cruz, CA, USA.
Ofer ShoshaniLudwig Institute for Cancer Research and Department of Cellular and Molecular Medicine, University of California at San Diego, La Jolla, CA, USA.
Aaron AslanianDepartment of Chemical Physiology, The Scripps Research Institute, La Jolla, CA, USA.
Moira A McMahonLudwig Institute for Cancer Research and Department of Cellular and Molecular Medicine, University of California at San Diego, La Jolla, CA, USA.
Ah Young LeeLudwig Institute for Cancer Research and Department of Cellular and Molecular Medicine, University of California at San Diego, La Jolla, CA, USA.
Daniele FachinettiLudwig Institute for Cancer Research and Department of Cellular and Molecular Medicine, University of California at San Diego, La Jolla, CA, USA.ORCID http://orcid.org/0000-0002-8795-6771
John R YatesDepartment of Chemical Physiology, The Scripps Research Institute, La Jolla, CA, USA.ORCID http://orcid.org/0000-0001-5267-1672
Bing RenLudwig Institute for Cancer Research and Department of Cellular and Molecular Medicine, University of California at San Diego, La Jolla, CA, USA.ORCID http://orcid.org/0000-0002-5435-1127
Don W ClevelandLudwig Institute for Cancer Research and Department of Cellular and Molecular Medicine, University of California at San Diego, La Jolla, CA, USA. dcleveland@ucsd.edu.ORCID http://orcid.org/0000-0002-1934-3682
Ludwig Cancer Research · USLudwig Cancer Research · BEScripps Research Institute · USCentre National de la Recherche Scientifique · FRIonis Pharmaceuticals (United States) · USUniversity of California, Santa Cruz · US

Funding

Mechanisms of chromosome segregation, aneuploidy, and tumorigenesisR35GM122476 · NIGMS · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI Don W Cleveland · 2017 to 2026
$9.0M
Mammalian Centromere AssemblyR01GM074150 · NIGMS · LUDWIG INSTITUTE FOR CANCER RES LTD · PI CLEVELAND, DON W · 2006 to 2016
$3.7M
NIGMS NIH HHS R01 GM074150NIGMS NIH HHS R35 GM122476
6 · The paper itself

Abstract

Chromatin assembled with the histone H3 variant CENP-A is the heritable epigenetic determinant of human centromere identity. Using genome-wide mapping and reference models for 23 human centromeres, CENP-A binding sites are identified within the megabase-long, repetitive α-satellite DNAs at each centromere. CENP-A is shown in early G1 to be assembled into nucleosomes within each centromere and onto 11,390 transcriptionally active sites on the chromosome arms. DNA replication is demonstrated to remove ectopically loaded, non-centromeric CENP-A. In contrast, tethering of centromeric CENP-A to the sites of DNA replication through the constitutive centromere associated network (CCAN) is shown to enable precise reloading of centromere-bound CENP-A onto the same DNA sequences as in its initial prereplication loading. Thus, DNA replication acts as an error correction mechanism for maintaining centromere identity through its removal of non-centromeric CENP-A coupled with CCAN-mediated retention and precise reloading of centromeric CENP-A.

Indexed as

CentromereCentromere Protein AChromatinChromosomal Proteins, Non-HistoneChromosomes, HumanDNA ReplicationG1 PhaseHeLa CellsHistonesHumansNucleosomesCentromere Protein AChromatinChromosomal Proteins, Non-HistoneHistonesNucleosomes

Identifiers

PMID31160708
PMCPMC7015266
OpenAlexW2948322052

What OpenQuestion holds

Textmetadata
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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.