Evidence map›Paper›PMID 15371340›Full record

ArticleGenes & development2004

A conserved protein network controls assembly of the outer kinetochore and its ability to sustain tension.

Iain M Cheeseman, Sherry Niessen, Scott Anderson, Francie Hyndman, John R Yates, Karen Oegema, Arshad Desai

Open access · diamondAbstract read
In one paragraph

Article in Genes & development, 2004. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 252 papers.

0numbers the graph read from it
0cells of the map it votes in
252citing papers in PubMed
–field-weighted citation impact
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

252 citing papers in PubMed, 410 citations in OpenAlex.

  1. Dual Roads of CENP-A for Centromere Identification.BioEssays : news and reviews in molecular, cellular and developmental biology · 2026
    Review
  2. Article
  3. 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
  4. Article
  5. Article
  6. Article
  7. Review
  8. Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. Article
  14. The Loss-Function ofSensors (Basel, Switzerland) · 2023
    Article
  15. Article
  16. Article
  17. Cell cycle control of kinetochore assembly.Nucleus (Austin, Tex.) · 2022
    Review
  18. Article
  19. Article
  20. Review

192 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

7 authors at 2 institutions in 1 country.

Iain M CheesemanLudwig Institute for Cancer Research, La Jolla, California 92093, USA. icheeseman@ucsd.edu
Sherry Niessen
Scott Anderson
Francie Hyndman
John R Yates
Karen Oegema
Arshad Desai
Scripps Research Institute · USLudwig Cancer Research · US

Funding

ZDS2P REGULATES SWE1P-DEPENDENT POLARIZED CELL GROWTH IN S CEREVISIAEP41RR011823 · NCRR · UNIVERSITY OF WASHINGTON · PI DAVIS, TRACY · 1996 to 2011
$24.7M
NCRR NIH HHS P41 RR011823NCRR NIH HHS P41 RR11823
6 · The paper itself

Abstract

Kinetochores play an essential role in chromosome segregation by forming dynamic connections with spindle microtubules. Here, we identify a set of 10 copurifying kinetochore proteins from Caenorhabditis elegans, seven of which were previously uncharacterized. Using in vivo assays to monitor chromosome segregation, kinetochore assembly, and the mechanical stability of chromosome-microtubule attachments, we show that this copurifying protein network plays a central role at the kinetochore-microtubule interface. In addition, our analysis suggests that the network is comprised of three groups of proteins that contribute in distinct ways to this interface: KNL proteins act after the assembly of centromeric chromatin to generate the core of the microtubule-binding interface, MIS proteins control the rate and extent of formation of this interface, and NDC proteins are necessary to sustain tension during interactions with spindle microtubules. We also purify a similar set of associated proteins from human cells that includes four novel proteins and has recognizable homologs from each functional class. Thus, this protein network is a conserved constituent of the outer kinetochore, and the functions defined by our analysis in C. elegans are likely to be widely relevant.

Indexed as

Amino Acid SequenceAnimalsCaenorhabditis elegansCaenorhabditis elegans ProteinsCell Cycle ProteinsChromosomal Proteins, Non-HistoneChromosome SegregationConserved SequenceEmbryo, NonmammalianHeLa CellsHumansKinetochoresMicrotubule-Associated ProteinsMitosisMutationNuclear ProteinsCaenorhabditis elegans ProteinsCell Cycle Proteinscentromere protein CChromosomal Proteins, Non-HistoneKNL-1 protein, C elegansKNL-3 protein, C elegansMicrotubule-Associated ProteinsMIS12 protein, humanNDC-80 protein, C elegansNuclear ProteinsNUF2 protein, humanRecombinant Proteins

Identifiers

PMID15371340
PMCPMC517519
OpenAlexW2099009321

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.