Evidence map›Paper›PMID 10494832›Full record

ReviewBiological chemistry

Chimeric restriction enzymes: what is next?

S Chandrasegaran, J Smith

Abstract readReview
In one paragraph

Review in Biological chemistry. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 29 papers.

0numbers the graph read from it
0cells of the map it votes in
29citing papers in PubMed
2.1field-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

29 citing papers in PubMed, 85 citations in OpenAlex.

  1. Gene Editing and Human iPSCs in Cardiovascular and Metabolic Diseases.Advances in experimental medicine and biology · 2023
    Article
  2. Points of View on the Tools for Genome/Gene Editing.International journal of molecular sciences · 2021
    Review
  3. Article
  4. Article
  5. Genome editing: a robust technology for human stem cells.Cellular and molecular life sciences : CMLS · 2017
    Review
  6. CRISPR-Cas Genome Surgery in Ophthalmology.Translational vision science & technology · 2017
    Review
  7. Review
  8. Review
  9. Article
  10. Article
  11. Article
  12. Zinc-finger nuclease-induced gene repair with oligodeoxynucleotides: wanted and unwanted target locus modifications.Molecular therapy : the journal of the American Society of Gene Therapy · 2010
    Article
  13. Article
  14. Article
  15. Article
  16. Review
  17. Article
  18. Review
  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

2 authors at 1 institution in 1 country.

S ChandrasegaranDepartment of Environmental Health Sciences, School of Public Health, The Johns Hopkins University, Baltimore, MD 21205, USA.
J Smith
Johns Hopkins University · US

Funding

HYBRID ENDONUCLEASES FOR GENOMIC RESEARCH AND ANALYSISR01GM053923 · NIGMS · JOHNS HOPKINS UNIVERSITY · PI CHANDRASEGARAN, SRINIVASAN · 1996 to 2003
$1.1M
NIGMS NIH HHS GM 53923NIGMS NIH HHS R01 GM053923
6 · The paper itself

Abstract

Chimeric restriction enzymes are a novel class of engineered nucleases in which the non-specific DNA cleavage domain of Fokl (a type IIS restriction endonuclease) is fused to other DNA-binding motifs. The latter include the three common eukaryotic DNA-binding motifs, namely the helix-turn-helix motif, the zinc finger motif and the basic helix-loop-helix protein containing a leucine zipper motif. Such chimeric nucleases have been shown to make specific cuts in vitro very close to the expected recognition sequences. The most important chimeric nucleases are those based on zinc finger DNA-binding proteins because of their modular structure. Recently, one such chimeric nuclease, Zif-QQR-F(N) was shown to find and cleave its target in vivo. This was tested by microinjection of DNA substrates and the enzyme into frog oocytes (Carroll et al., 1999). The injected enzyme made site-specific double-strand breaks in the targets even after assembly of the DNA into chromatin. In addition, this cleavage activated the target molecules for efficient homologous recombination. Since the recognition specificity of zinc fingers can be manipulated experimentally, chimeric nucleases could be engineered so as to target a specific site within a genome. The availability of such engineered chimeric restriction enzymes should make it feasible to do genome engineering, also commonly referred to as gene therapy.

Indexed as

DNA Restriction EnzymesHydrolysisRecombinant Fusion ProteinsRecombination, GeneticSubstrate SpecificityDNA Restriction EnzymesRecombinant Fusion Proteins

Identifiers

PMID10494832
PMCPMC4033837
OpenAlexW2005881308

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.