Evidence map›Paper›PMID 19656849›Full record

ArticleMolecular biology of the cell2009

Function and assembly of DNA looping, clustering, and microtubule attachment complexes within a eukaryotic kinetochore.

Marybeth Anderson, Julian Haase, Elaine Yeh, Kerry Bloom

Open access · greenAbstract read
In one paragraph

Article in Molecular biology of the cell, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 53 papers.

0numbers the graph read from it
0cells of the map it votes in
53citing papers in PubMed
2.7field-weighted citation impact, top 10% 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

53 citing papers in PubMed, 59 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. The regulation of chromosome segregation via centromere loops.Critical reviews in biochemistry and molecular biology · 2019
    Review
  6. Article
  7. Article
  8. Point centromere activity requires an optimal level of centromeric noncoding RNA.Proceedings of the National Academy of Sciences of the United States of America · 2019
    Article
  9. Fork pausing allows centromere DNA loop formation and kinetochore assembly.Proceedings of the National Academy of Sciences of the United States of America · 2018
    Article
  10. Review
  11. Article
  12. Article
  13. Article
  14. Stepwise unfolding supports a subunit model for vertebrate kinetochores.Proceedings of the National Academy of Sciences of the United States of America · 2017
    Article
  15. Article
  16. Article
  17. Article
  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

4 authors at 1 institution in 1 country.

Marybeth AndersonDepartment of Biology, University of North Carolina at Chapel Hill, Chapel Hill, NC 27599-3280, USA.
Julian Haase
Elaine Yeh
Kerry Bloom
University of North Carolina at Chapel Hill · US

Funding

Structure and Function of a Eukaryotic CentromereR01GM032238 · NIGMS · UNIV OF NORTH CAROLINA CHAPEL HILL · PI BLOOM, KERRY S · 1985 to 2025
$6.2M
NIGMS NIH HHS R01 GM032238NIGMS NIH HHS R01 GM-32238
6 · The paper itself

Abstract

The kinetochore is a complex protein-DNA assembly that provides the mechanical linkage between microtubules and the centromere DNA of each chromosome. Centromere DNA in all eukaryotes is wrapped around a unique nucleosome that contains the histone H3 variant CENP-A (Cse4p in Saccharomyces cerevisiae). Here, we report that the inner kinetochore complex (CBF3) is required for pericentric DNA looping at the Cse4p-containing nucleosome. DNA within the pericentric loop occupies a spatially confined area that is radially displaced from the interpolar central spindle. Microtubule-binding kinetochore complexes are not involved in pericentric DNA looping but are required for the geometric organization of DNA loops around the spindle microtubules in metaphase. Thus, the mitotic segregation apparatus is a composite structure composed of kinetochore and interpolar microtubules, the kinetochore, and organized pericentric DNA loops. The linkage of microtubule-binding to centromere DNA-looping complexes positions the pericentric chromatin loops and stabilizes the dynamic properties of individual kinetochore complexes in mitosis.

Indexed as

Cell Cycle ProteinsChromosomal Proteins, Non-HistoneDNA-Binding ProteinsDNA, FungalEukaryotic CellsFluorescence Recovery After PhotobleachingGreen Fluorescent ProteinsKinetochoresMicrotubulesMitosisNuclear ProteinsNucleosomesSaccharomyces cerevisiaeSaccharomyces cerevisiae ProteinsSpindle ApparatusCBF2 protein, S cerevisiaeCell Cycle ProteinsChromosomal Proteins, Non-HistoneCSE4 protein, S cerevisiaeDNA-Binding ProteinsDNA, FungalGreen Fluorescent ProteinsMTW1 protein, S cerevisiaeNDC80 protein, S cerevisiaeNuclear ProteinsNucleosomesNUF2 protein, S cerevisiaeSaccharomyces cerevisiae Proteins

Identifiers

PMID19656849
PMCPMC2754927
OpenAlexW2165606404

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.