Evidence map›Paper›PMID 23657009›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2013

Phosphorylation of the CENP-A amino-terminus in mitotic centromeric chromatin is required for kinetochore function.

Damien Goutte-Gattat, Muhammad Shuaib, Khalid Ouararhni, Thierry Gautier, Dimitrios A Skoufias, Ali Hamiche, Stefan Dimitrov

Open access · bronzeAbstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 38 papers.

0numbers the graph read from it
0cells of the map it votes in
38citing papers in PubMed
3.3field-weighted citation impact, top 7% 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

38 citing papers in PubMed, 59 citations in OpenAlex.

  1. Structure and function of the centromere and inner kinetochore.Nature reviews. Molecular cell biology · 2026
    Review
  2. Article
  3. Article
  4. Review
  5. Article
  6. Kinetochore assembly throughout the cell cycle.Seminars in cell & developmental biology · 2021
    Article
  7. Article
  8. Review
  9. Article
  10. Review
  11. Epigenetic regulation of centromere function.Cellular and molecular life sciences : CMLS · 2020
    Review
  12. Article
  13. Article
  14. Review
  15. Review
  16. Review
  17. Article
  18. Review
  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

7 authors at 5 institutions in 1 country.

Damien Goutte-GattatInstitut National de la Santé et de la Recherche Médicale, Université Joseph-Fourier-Grenoble 1, Institut Albert Bonniot, Unité 823, 38042 Grenoble Cedex 9, France.
Muhammad Shuaib
Khalid Ouararhni
Thierry Gautier
Dimitrios A Skoufias
Ali Hamiche
Stefan Dimitrov
Institut de génétique et de biologie moléculaire et cellulaire · FRUniversité Joseph Fourier · FRCommissariat à l'Énergie Atomique et aux Énergies Alternatives · FRInserm · FRUniversité de Strasbourg · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The role of the mitotic phosphorylation of the amino (NH2) terminus of Centromere Protein A (CENP-A), the histone variant epigenetic centromeric marker, remains elusive. Here, we show that the NH2 terminus of human CENP-A is essential for mitotic progression and that localization of CENP-C, another key centromeric protein, requires only phosphorylation of the CENP-A NH2 terminus, and is independent of the CENP-A NH2 terminus length and amino acid sequence. Mitotic CENP-A nucleosomal complexes contain CENP-C and phosphobinding 14-3-3 proteins. In contrast, mitotic nucleosomal complexes carrying nonphosphorylatable CENP-A-S7A contained only low levels of CENP-C and no detectable 14-3-3 proteins. Direct interactions between the phosphorylated form of CENP-A and 14-3-3 proteins as well as between 14-3-3 proteins and CENP-C were demonstrated. Taken together, our results reveal that 14-3-3 proteins could act as specific mitotic "bridges," linking phosphorylated CENP-A and CENP-C, which are necessary for the platform function of CENP-A centromeric chromatin in the assembly and maintenance of active kinetochores.

Indexed as

14-3-3 ProteinsAmino Acid SubstitutionAutoantigensCentromere Protein AChromosomal Proteins, Non-HistoneHeLa CellsHumansKinetochoresMitosisMutation, MissenseNucleosomesPhosphorylationProtein Structure, Tertiary14-3-3 ProteinsAutoantigensCENPA protein, humanCentromere Protein Acentromere protein CChromosomal Proteins, Non-HistoneNucleosomes

Identifiers

PMID23657009
PMCPMC3666736
OpenAlexW2056902844

What OpenQuestion holds

Textmetadata
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.