Evidence map›Paper›PMID 19952142›Full record

ArticleGenome research2010

Targeted chromosomal deletions in human cells using zinc finger nucleases.

Hyung Joo Lee, Eunji Kim, Jin-Soo Kim

Open access · bronzeAbstract readEvaluation Study
In one paragraph

Article in Genome research, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 147 papers.

0numbers the graph read from it
0cells of the map it votes in
147citing 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

147 citing papers in PubMed, 251 citations in OpenAlex.

  1. Review
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  6. CRISPR-based editing strategies to rectifyMolecular therapy. Nucleic acids · 2024
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  7. Multiplex Editing of theThe CRISPR journal · 2023
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  8. Review
  9. Article
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  11. Targeted genomic translocations and inversions generated using a paired prime editing strategy.Molecular therapy : the journal of the American Society of Gene Therapy · 2023
    Article
  12. Review
  13. Review
  14. Speciation and adaptation research meets genome editing.Philosophical transactions of the Royal Society of London. Series B, Biological sciences · 2022
    Review
  15. Review
  16. Article
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  18. Article
  19. Review
  20. Review

87 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

3 authors at 1 institution in 1 country.

Hyung Joo LeeDepartment of Chemistry, Seoul National University, Seoul, South Korea.
Eunji Kim
Jin-Soo Kim
Seoul National University · KR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

We present a novel approach for generating targeted deletions of genomic segments in human and other eukaryotic cells using engineered zinc finger nucleases (ZFNs). We found that ZFNs designed to target two different sites in a human chromosome could introduce two concurrent DNA double-strand breaks (DSBs) in the chromosome and give rise to targeted deletions of the genomic segment between the two sites. Using this method in human cells, we were able to delete predetermined genomic DNA segments in the range of several-hundred base pairs (bp) to 15 mega-bp at frequencies of 10(-3) to 10(-1). These high frequencies allowed us to isolate clonal populations of cells, in which the target chromosomal segments were deleted, by limiting dilution. Sequence analysis revealed that many of the deletion junctions contained small insertions or deletions and microhomologies, indicative of DNA repair via nonhomologous end-joining. Unlike other genome engineering tools such as recombinases and meganucleases, ZFNs do not require preinsertion of target sites into the genome and allow precise manipulation of endogenous genomic scripts in animal and plant cells. Thus, ZFN-induced genomic deletions should be broadly useful as a novel method in biomedical research, biotechnology, and gene therapy.

Indexed as

Chromosome DeletionDNA Breaks, Double-StrandedGene TargetingZinc FingersCell LineChromosomes, HumanCloning, MolecularEndonucleasesGenetic EngineeringGenetic TechniquesHumansPolymerase Chain ReactionReceptors, CCR2Receptors, CCR5Sequence Analysis, DNACCR2 protein, humanEndonucleasesReceptors, CCR2Receptors, CCR5

Identifiers

PMID19952142
PMCPMC2798833
OpenAlexW1977036449

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.