Evidence map›Paper›PMID 11086012›Full record

ArticleThe Journal of cell biology2000

Chromatin assembly at kinetochores is uncoupled from DNA replication.

R D Shelby, K Monier, K F Sullivan

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of cell biology, 2000. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 115 papers.

0numbers the graph read from it
0cells of the map it votes in
115citing papers in PubMed
20.2field-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

115 citing papers in PubMed, 228 citations in OpenAlex.

  1. Structure and function of the centromere and inner kinetochore.Nature reviews. Molecular cell biology · 2026
    Review
  2. Article
  3. 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
  4. Review
  5. Review
  6. Review
  7. Article
  8. Centromere Identity and the Regulation of Chromosome Segregation.Frontiers in cell and developmental biology · 2022
    Review
  9. Review
  10. Review
  11. Review
  12. Review
  13. Article
  14. Review
  15. Epigenetic regulation of centromere function.Cellular and molecular life sciences : CMLS · 2020
    Review
  16. Review
  17. Review
  18. Article
  19. The regulation of chromosome segregation via centromere loops.Critical reviews in biochemistry and molecular biology · 2019
    Review
  20. Article

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

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 at 1 institution in 1 country.

R D ShelbyDepartment of Cell Biology, The Scripps Research Institute, La Jolla, California 92037, USA.
K Monier
K F Sullivan
Scripps Research Institute · US

Funding

TARGETING AND FUNCTION OF HUMAN CENTROMERE PROTEIN-AR01GM039068 · NIGMS · SCRIPPS RESEARCH INSTITUTE · PI SULLIVAN, KEVIN F · 1994 to 2004
$1.9M
MOLECULAR ANALYSIS OF MAMMALIAN KINETOCHORE STRUCTURER29GM039068 · NIGMS · SCRIPPS RESEARCH INSTITUTE · PI SULLIVAN, KEVIN F · 1988 to 1992
–
NIGMS NIH HHS GM39068NIGMS NIH HHS R01 GM039068
6 · The paper itself

Abstract

The specification of metazoan centromeres does not depend strictly on centromeric DNA sequences, but also requires epigenetic factors. The mechanistic basis for establishing a centromeric "state" on the DNA remains unclear. In this work, we have directly examined replication timing of the prekinetochore domain of human chromosomes. Kinetochores were labeled by expression of epitope-tagged CENP-A, which stably marks prekinetochore domains in human cells. By immunoprecipitating CENP-A mononucleosomes from synchronized cells pulsed with [(3)H]thymidine we demonstrate that CENP-A-associated DNA is replicated in mid-to-late S phase. Cytological analysis of DNA replication further demonstrated that centromeres replicate asynchronously in parallel with numerous other genomic regions. In contrast, quantitative Western blot analysis demonstrates that CENP-A protein synthesis occurs later, in G2. Quantitative fluorescence microscopy and transient transfection in the presence of aphidicolin, an inhibitor of DNA replication, show that CENP-A can assemble into centromeres in the absence of DNA replication. Thus, unlike most genomic chromatin, histone synthesis and assembly are uncoupled from DNA replication at the kinetochore. Uncoupling DNA replication from CENP-A synthesis suggests that regulated chromatin assembly or remodeling could play a role in epigenetic centromere propagation.

Indexed as

AutoantigensCell CycleCentromereCentromere Protein AChromatinChromosomal Proteins, Non-HistoneDNA ReplicationEpitopesGene ExpressionHeLa CellsHumansKinetochoresRNA, MessengerTransfectionAutoantigensCENPA protein, humanCentromere Protein AChromatinChromosomal Proteins, Non-HistoneEpitopesRNA, Messenger

Identifiers

PMID11086012
PMCPMC2174364
OpenAlexW2041808377

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-SA
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.