Evidence map›Paper›PMID 15542852›Full record

ArticleMolecular and cellular biology2004

Deficiency in SNM1 abolishes an early mitotic checkpoint induced by spindle stress.

Shamima Akhter, Christopher T Richie, Jian Min Deng, Eric Brey, Xiaoshan Zhang, Charles Patrick, Richard R Behringer, Randy J Legerski

Open access · greenAbstract read
In one paragraph

Article in Molecular and cellular biology, 2004. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed
1.3field-weighted citation impact, top 23% 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

22 citing papers in PubMed, 32 citations in OpenAlex.

  1. Structure and Function of SNM1 Family Nucleases.Advances in experimental medicine and biology · 2023
    Review
  2. Review
  3. Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. The multifunctional SNM1 gene family: not just nucleases.Future oncology (London, England) · 2010
    Review
  12. SNM1A acts downstream of ATM to promote the G1 cell cycle checkpoint.Biochemical and biophysical research communications · 2008
    Article
  13. Article
  14. Article
  15. Article
  16. Mammalian SNM1 is required for genome stability.Molecular genetics and metabolism · 2008
    Article
  17. The hSNM1 protein is a DNA 5'-exonuclease.Nucleic acids research · 2007
    Article
  18. Article
  19. 53BP1 and p53 synergize to suppress genomic instability and lymphomagenesis.Proceedings of the National Academy of Sciences of the United States of America · 2006
    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

8 authors at 1 institution in 1 country.

Shamima AkhterUniversity of Texas M. D. Anderson Cancer Center, Department of Molecular Genetics, 1515 Holcombe Blvd., Houston, TX 77030, USA.
Christopher T Richie
Jian Min Deng
Eric Brey
Xiaoshan Zhang
Charles Patrick
Richard R Behringer
Randy J Legerski
The University of Texas MD Anderson Cancer Center · US

Funding

Tumor Evolution and Metastasis ProgramP30CA016672 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI Scott Kopetz · 1985 to 2026
$290.8M
Pilot Project ProgramP30ES007784 · NIEHS · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI RICHIE, ELLEN R · 1996 to 2011
$16.4M
University of Texas SPORE in Prostate CancerP50CA090270 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI LOGOTHETIS, CHRISTOPHER J. · 2001 to 2007
$13.6M
ISOLATION AND ANALYSIS OF HUMAN DNA REPAIR GENESR01CA052461 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI LEGERSKI, RANDY J · 1992 to 2006
$1.6M
The Role of Artemis in Cellular Responses to DNA DamageR01CA096574 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI LEGERSKI, RANDY J · 2004 to 2008
$1.5M
NCI NIH HHS CA16672NCI NIH HHS CA52461NCI NIH HHS CA90270NCI NIH HHS CA96574NCI NIH HHS P30 CA016672NCI NIH HHS P50 CA090270NCI NIH HHS R01 CA052461NCI NIH HHS R01 CA096574NIEHS NIH HHS ES07784NIEHS NIH HHS P30 ES007784
6 · The paper itself

Abstract

Spindle poisons represent an important class of anticancer drugs that act by interfering with microtubule polymerization and dynamics and thereby induce mitotic checkpoints and apoptosis. Here we show that mammalian SNM1 functions in an early mitotic stress checkpoint that is distinct from the well-characterized spindle checkpoint that regulates the metaphase-to-anaphase transition. Specifically, we found that compared to wild-type cells, Snm1-deficient mouse embryonic fibroblasts exposed to spindle poisons exhibited elevated levels of micronucleus formation, decreased mitotic delay, a failure to arrest in mitosis prior to chromosome condensation, supernumerary centrosomes, and decreased viability. In addition, we show that both Snm1 and 53BP1, previously shown to interact, coimmunoprecipitate with components of the anaphase-promoting complex (APC)/cyclosome. These findings suggest that Snm1 is a component of a mitotic stress checkpoint that negatively targets the APC prior to chromosome condensation.

Indexed as

MitosisSpindle ApparatusAnaphaseAnimalsAntineoplastic AgentsApoptosisCDC2-CDC28 KinasesCell LineCell NucleusChromosomesDNA-Binding ProteinsDNA, ComplementaryEndodeoxyribonucleasesFlow CytometryHeLa CellsHumansAntineoplastic AgentsCDC2-CDC28 KinasesDNA-Binding ProteinsDNA, ComplementaryEndodeoxyribonucleasesIfi202b protein, mouseIntracellular Signaling Peptides and ProteinsNocodazoleNuclear ProteinsPhosphoproteinsPSO2 protein, S cerevisiaeRNA, Small InterferingSaccharomyces cerevisiae ProteinsTP53BP1 protein, humanTumor Suppressor p53-Binding Protein 1

Identifiers

PMID15542852
PMCPMC529044
OpenAlexW2128962134

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.