Evidence map›Paper›PMID 16533944›Full record

ArticleThe Journal of cell biology2006

The selective continued linkage of centromeres from mitosis to interphase in the absence of mammalian separase.

Kazuki Kumada, Ryoji Yao, Tokuichi Kawaguchi, Mika Karasawa, Yutaka Hoshikawa, Koji Ichikawa, Yoshinobu Sugitani, Issei Imoto, Johji Inazawa, Minoru Sugawara and 2 more

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of cell biology, 2006. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 36 papers.

0numbers the graph read from it
0cells of the map it votes in
36citing papers in PubMed
4.1field-weighted citation impact, top 6% 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

36 citing papers in PubMed, 72 citations in OpenAlex.

  1. Article
  2. The Effect ofLife (Basel, Switzerland) · 2025
    Article
  3. Article
  4. Article
  5. Role of chromosomal cohesion and separation in aneuploidy and tumorigenesis.Cellular and molecular life sciences : CMLS · 2024
    Review
  6. Building the right centriole for each cell type.The Journal of cell biology · 2018
    Review
  7. Article
  8. Cohesin Mutations in Cancer.Cold Spring Harbor perspectives in medicine · 2016
    Review
  9. Article
  10. Article
  11. Article
  12. Article
  13. Article
  14. Review
  15. Review
  16. Article
  17. Article
  18. Article
  19. Article
  20. Review
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

12 authors at 4 institutions in 1 country.

Kazuki KumadaJapanese Foundation for Cancer Research, Cancer Institute, Tokyo 135-8550, Japan.
Ryoji Yao
Tokuichi Kawaguchi
Mika Karasawa
Yutaka Hoshikawa
Koji Ichikawa
Yoshinobu Sugitani
Issei Imoto
Johji Inazawa
Minoru Sugawara
Mitsuhiro Yanagida
Tetsuo Noda
Japanese Foundation For Cancer Research · JPTohoku University · JPTokyo Medical and Dental University · JPKyoto University · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Separase is an evolutionarily conserved protease that is essential for chromosome segregation and cleaves cohesin Scc1/Rad21, which joins the sister chromatids together. Although mammalian separase also functions in chromosome segregation, our understanding of this process in mammals is still incomplete. We generated separase knockout mice, reporting an essential function for mammalian separase. Separase-deficient mouse embryonic fibroblasts exhibited severely restrained increases in cell number, polyploid chromosomes, and amplified centrosomes. Chromosome spreads demonstrated that multiple chromosomes connected to a centromeric region. Live observation demonstrated that the chromosomes of separase-deficient cells condensed, but failed to segregate, although subsequent cytokinesis and chromosome decondensation proceeded normally. These results establish that mammalian separase is essential for the separation of centromeres, but not of the arm regions of chromosomes. Other cell cycle events, such as mitotic exit, DNA replication, and centrosome duplication appear to occur normally. We also demonstrated that heterozygous separase-deficient cells exhibited severely restrained increases in cell number with apparently normal mitosis in the absence of securin, which is an inhibitory partner of separase.

Indexed as

AnimalsCarrier ProteinsCell Cycle ProteinsCell ProliferationCells, CulturedCentromereCentrosomeChromosome SegregationCytokinesisEndopeptidasesFemaleFibroblastsInterphaseMaleMiceMice, KnockoutCarrier ProteinsCell Cycle ProteinsEndopeptidasesSecurinSeparase

Identifiers

PMID16533944
PMCPMC2063728
OpenAlexW2135317081

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.