Evidence map›Paper›PMID 12551952›Full record

ArticleThe Journal of cell biology2003

Rae1 is an essential mitotic checkpoint regulator that cooperates with Bub3 to prevent chromosome missegregation.

J Ramesh Babu, Karthik B Jeganathan, Darren J Baker, Xiaosheng Wu, Ningling Kang-Decker, Jan M van Deursen

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of cell biology, 2003. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 189 papers.

0numbers the graph read from it
0cells of the map it votes in
189citing papers in PubMed
7.4field-weighted citation impact, top 2% 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

189 citing papers in PubMed, 339 citations in OpenAlex.

  1. Review
  2. Review
  3. Advances in the understanding of nuclear pore complexes in human diseases.Journal of cancer research and clinical oncology · 2024
    Review
  4. Article
  5. The two sides of chromosomal instability: drivers and brakes in cancer.Signal transduction and targeted therapy · 2024
    Review
  6. Article
  7. Review
  8. Review
  9. Review
  10. [Progress in the Study of Spindle Assembly Checkpoint in Lung Cancer].Zhongguo fei ai za zhi = Chinese journal of lung cancer · 2023
    Article
  11. Review
  12. Article
  13. Review
  14. Article
  15. Article
  16. Article
  17. Review
  18. Review
  19. Article
  20. Review

129 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

6 authors at 1 institution in 1 country.

J Ramesh BabuDepartment of Pediatric and Adolescent Medicine, Mayo Clinic, Rochester, MN 55905, USA.
Karthik B Jeganathan
Darren J Baker
Xiaosheng Wu
Ningling Kang-Decker
Jan M van Deursen
Mayo Clinic in Florida · US

Funding

BUBRI in Normal and Neoplastic GrowthR01CA096985 · NCI · MAYO CLINIC ROCHESTER · PI BAKER, DARREN · 2002 to 2022
$6.2M
NUP98-HOXA9 AND AMLR01CA077262 · NCI · ST. JUDE CHILDREN'S RESEARCH HOSPITAL · PI VAN DEURSEN, JAN M. · 1998 to 2012
$3.9M
NCI NIH HHS R01 CA077262NCI NIH HHS R01 CA096985NCI NIH HHS R01 CA77262-01NCI NIH HHS R01 CA96985-1
6 · The paper itself

Abstract

The WD-repeat proteins Rae1 and Bub3 show extensive sequence homology, indicative of functional similarity. However, previous studies have suggested that Rae1 is involved in the mRNA export pathway and Bub3 in the mitotic checkpoint. To determine the in vivo roles of Rae1 and Bub3 in mammals, we generated knockout mice that have these genes deleted individually or in combination. Here we show that haplo-insufficiency of either Rae1 or Bub3 results in a similar phenotype involving mitotic checkpoint defects and chromosome missegregation. We also show that overexpression of Rae1 can correct for Rae1 haplo-insufficiency and, surprisingly, Bub3 haplo-insufficiency. Rae1-null and Bub3-null mice are embryonic lethal, although cells from these mice did not have a detectable defect in nuclear export of mRNA. Unlike null mice, compound haplo-insufficient Rae1/Bub3 mice are viable. However, cells from these mice exhibit much greater rates of premature sister chromatid separation and chromosome missegregation than single haplo-insufficient cells. Finally, we show that mice with mitotic checkpoint defects are more susceptible to dimethylbenzanthrene-induced tumorigenesis than wild-type mice. Thus, our data demonstrate a novel function for Rae1 and characterize Rae1 and Bub3 as related proteins with essential, overlapping, and cooperating roles in the mitotic checkpoint.

Indexed as

Active Transport, Cell NucleusAneuploidyAnimalsCell Cycle ProteinsCells, CulturedCell Transformation, NeoplasticChromosomal Proteins, Non-HistoneChromosome AberrationsChromosome SegregationFemaleFetusGene Expression Regulation, DevelopmentalGenes, cdcGenes, LethalGenetic Predisposition to DiseaseMaleBub3 protein, mouseCell Cycle ProteinsChromosomal Proteins, Non-HistoneNuclear Matrix-Associated ProteinsNucleocytoplasmic Transport ProteinsPoly-ADP-Ribose Binding ProteinsRae1 protein, mouseRNA, Messenger

Identifiers

PMID12551952
PMCPMC2172680
OpenAlexW2138968849

What OpenQuestion holds

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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.