Evidence map›Paper›PMID 20528238›Full record

ReviewFuture oncology (London, England)2010

The multifunctional SNM1 gene family: not just nucleases.

Yiyi Yan, Shamima Akhter, Xiaoshan Zhang, Randy Legerski

Open access · greenAbstract readReview
In one paragraph

Review in Future oncology (London, England), 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 24 papers.

0numbers the graph read from it
0cells of the map it votes in
24citing papers in PubMed
2.2field-weighted citation impact, top 13% 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

24 citing papers in PubMed, 40 citations in OpenAlex.

  1. Article
  2. Article
  3. Structure and Function of SNM1 Family Nucleases.Advances in experimental medicine and biology · 2023
    Review
  4. Article
  5. Article
  6. Article
  7. Review
  8. Article
  9. Article
  10. Review
  11. Article
  12. Review
  13. Article
  14. Article
  15. Review
  16. Repair of double-strand breaks by end joining.Cold Spring Harbor perspectives in biology · 2013
    Review
  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.

Yiyi YanDepartment of Genetics, University of Texas MD Anderson Cancer Center, 1515 Holcombe Boulevard, Houston, TX 77030, USA.
Shamima Akhter
Xiaoshan Zhang
Randy Legerski
The University of Texas MD Anderson Cancer Center · US

Funding

Recognition and processing of complex lesions by components from multiple DNAP01CA097175 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI NAIRN, RODNEY S · 2004 to 2014
$15.3M
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 CA096574NCI NIH HHS CA097175NCI NIH HHS P01 CA097175NCI NIH HHS R01 CA052461NCI NIH HHS R01 CA096574
6 · The paper itself

Abstract

The archetypical member of the SNM1 gene family was discovered 30 years ago in the budding yeast Saccharomyces cerevisiae. This small but ubiquitous gene family is characterized by metallo-beta-lactamase and beta-CASP domains, which together have been demonstrated to comprise a nuclease activity. Three mammalian members of this family, SNM1A, SNM1B/Apollo and Artemis, have been demonstrated to play surprisingly divergent roles in cellular metabolism. These pathways include variable (diversity) joining recombination, nonhomologous end-joining of double-strand breaks, DNA damage and mitotic cell cycle checkpoints, telomere maintenance and protein ubiquitination. Not all of these functions are consistent with a model in which these proteins act only as nucleases, and indicate that the SNM1 gene family encodes multifunctional products that can act in diverse biochemical pathways. In this article we discuss the various functions of SNM1A, SNM1B/Apollo and Artemis.

Indexed as

Multigene FamilyAnimalsCell Cycle ProteinsCross-Linking ReagentsDNA-Binding ProteinsDNA DamageDNA RepairDNA Repair EnzymesEndodeoxyribonucleasesEndonucleasesExodeoxyribonucleasesGenes, cdcGenetic Complementation TestHumansMammalsMiceCell Cycle ProteinsCross-Linking ReagentsDclre1a protein, mouseDCLRE1B protein, humanDCLRE1C protein, humanDNA-Binding ProteinsDNA Repair EnzymesEndodeoxyribonucleasesEndonucleasesExodeoxyribonucleasesNuclear ProteinsPSO2 protein, S cerevisiaeSaccharomyces cerevisiae ProteinsTumor Suppressor Proteins

Identifiers

PMID20528238
PMCPMC2904241
OpenAlexW2013132855

What OpenQuestion holds

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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.