Evidence map›Paper›PMID 24569350›Full record

ArticleNucleic acids research2014

Comprehensive analysis of the specificity of transcription activator-like effector nucleases.

Alexandre Juillerat, Gwendoline Dubois, Julien Valton, Séverine Thomas, Stefano Stella, Alan Maréchal, Stéphanie Langevin, Nassima Benomari, Claudia Bertonati, George H Silva and 5 more

Abstract read
In one paragraph

Article in Nucleic acids research, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 43 papers.

0numbers the graph read from it
0cells of the map it votes in
43citing 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

43 citing papers in PubMed.

  1. Article
  2. Review
  3. Article
  4. Review
  5. Review
  6. Detection of chromosomal alteration after infusion of gene-edited allogeneic CAR T cells.Molecular therapy : the journal of the American Society of Gene Therapy · 2023
    Article
  7. Review
  8. Review
  9. Article
  10. CRISPR/Cas9: a tool to eradicate HIV-1.AIDS research and therapy · 2022
    Review
  11. Article
  12. Efficient multitool/multiplex gene engineering with TALE-BE.Frontiers in bioengineering and biotechnology · 2022
    Article
  13. Article
  14. Article
  15. The Journal of neuroscience : the official journal of the Society for Neuroscience · 2021
    Article
  16. Description of CRISPR/Cas9 development and its prospect in hepatocellular carcinoma treatment.Journal of experimental & clinical cancer research : CR · 2020
    Review
  17. Article
  18. Article
  19. Review
  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

15 authors.

Alexandre JuilleratCellectis S.A., 8 Rue de la Croix Jarry, 75013 Paris, France, Structural Biology and Biocomputing Programme, Spanish National Cancer Research Centre, Macromolecular Crystallography Group, c/Melchor Fdez. Almagro 3, 28029 Madrid, Spain and Structural Biology Group, Novo Nordisk Foundation Center for Protein Research, Faculty of Health and Medical Sciences, University of Copenhagen, Blegdamsvej 3B, 2200 Copenhagen, Denmark.
Gwendoline Dubois
Julien Valton
Séverine Thomas
Stefano Stella
Alan Maréchal
Stéphanie Langevin
Nassima Benomari
Claudia Bertonati
George H Silva
Fayza Daboussi
Jean-Charles Epinat
Guillermo Montoya
Aymeric Duclert
Philippe Duchateau

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

A key issue when designing and using DNA-targeting nucleases is specificity. Ideally, an optimal DNA-targeting tool has only one recognition site within a genomic sequence. In practice, however, almost all designer nucleases available today can accommodate one to several mutations within their target site. The ability to predict the specificity of targeting is thus highly desirable. Here, we describe the first comprehensive experimental study focused on the specificity of the four commonly used repeat variable diresidues (RVDs; NI:A, HD:C, NN:G and NG:T) incorporated in transcription activator-like effector nucleases (TALEN). The analysis of >15 500 unique TALEN/DNA cleavage profiles allowed us to monitor the specificity gradient of the RVDs along a TALEN/DNA binding array and to present a specificity scoring matrix for RVD/nucleotide association. Furthermore, we report that TALEN can only accommodate a relatively small number of position-dependent mismatches while maintaining a detectable activity at endogenous loci in vivo, demonstrating the high specificity of these molecular tools. We thus envision that the results we provide will allow for more deliberate choices of DNA binding arrays and/or DNA targets, extending our engineering capabilities.

Indexed as

Amino AcidsAnimalsBase SequenceCHO CellsCricetinaeCricetulusDeoxyribonucleasesDNADNA-Binding ProteinsDNA CleavageMutationProtein Array AnalysisProtein EngineeringYeastsAmino AcidsDeoxyribonucleasesDNADNA-Binding Proteins

Identifiers

PMID24569350
PMCPMC4005648

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.