Evidence map›Paper›PMID 23979943›Full record

ArticleG3 (Bethesda, Md.)2013

Targeted deletion and inversion of tandemly arrayed genes in Arabidopsis thaliana using zinc finger nucleases.

Yiping Qi, Xiaohong Li, Yong Zhang, Colby G Starker, Nicholas J Baltes, Feng Zhang, Jeffry D Sander, Deepak Reyon, J Keith Joung, Daniel F Voytas

Open access · goldAbstract read
In one paragraph

Article in G3 (Bethesda, Md.), 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 32 papers.

0numbers the graph read from it
0cells of the map it votes in
32citing papers in PubMed
5.2field-weighted citation impact, top 4% 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

32 citing papers in PubMed, 89 citations in OpenAlex.

  1. Review
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  8. Multiplex Editing of theThe CRISPR journal · 2023
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  12. Review
  13. Genome Editing in Agriculture: Technical and Practical Considerations.International journal of molecular sciences · 2019
    Review
  14. Review
  15. Article
  16. Review
  17. Genetically modified (GM) crops: milestones and new advances in crop improvement.TAG. Theoretical and applied genetics. Theoretische und angewandte Genetik · 2016
    Review
  18. Article
  19. Review
  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

10 authors at 5 institutions in 2 countries.

Yiping QiDepartment of Genetics, Cell Biology & Development and Center for Genome Engineering, University of Minnesota, Minneapolis, Minnesota 55455.
Xiaohong Li
Yong Zhang
Colby G Starker
Nicholas J Baltes
Feng Zhang
Jeffry D Sander
Deepak Reyon
J Keith Joung
Daniel F Voytas
University of Minnesota · USCenter for Cancer Research · USHarvard University · USMassachusetts General Hospital · USUniversity of Electronic Science and Technology of China · CN

Funding

ADVANCING ZINC FINGER NUCLEASES FOR TARGETED GENOME MANIPULATIONR01GM088040 · NIGMS · MASSACHUSETTS GENERAL HOSPITAL · PI JOUNG, J. KEITH, PETERSON, RANDALL T · 2009 to 2016
$4.5M
Advancing stem cell technologies using engineered zinc finger proteinsDP1GM105378 · NIGMS · MASSACHUSETTS GENERAL HOSPITAL · PI JOUNG, J. KEITH · 2012 to 2014
$2.6M
DNA targeting by TAL effectorsR01GM098861 · NIGMS · IOWA STATE UNIVERSITY · PI BOGDANOVE, ADAM J, STODDARD, BARRY L. · 2011 to 2014
$2.0M
NCCDPHP CDC HHS DP1 GM105378NIGMS NIH HHS DP1 GM105378NIGMS NIH HHS R01 GM088040
6 · The paper itself

Abstract

Tandemly arrayed genes (TAGs) or gene clusters are prevalent in higher eukaryotic genomes. For example, approximately 17% of genes are organized in tandem in the model plant Arabidopsis thaliana. The genetic redundancy created by TAGs presents a challenge for reverse genetics. As molecular scissors, engineered zinc finger nucleases (ZFNs) make DNA double-strand breaks in a sequence-specific manner. ZFNs thus provide a means to delete TAGs by creating two double-strand breaks in the gene cluster. Using engineered ZFNs, we successfully targeted seven genes from three TAGs on two Arabidopsis chromosomes, including the well-known RPP4 gene cluster, which contains eight resistance (R) genes. The resulting gene cluster deletions ranged from a few kb to 55 kb with frequencies approximating 1% in somatic cells. We also obtained large chromosomal deletions of ~9 Mb at approximately one tenth the frequency, and gene cluster inversions and duplications also were achieved. This study demonstrates the ability to use sequence-specific nucleases in plants to make targeted chromosome rearrangements and create novel chimeric genes for reverse genetics and biotechnology.

Indexed as

Chromosome DeletionGenes, PlantTandem Repeat SequencesArabidopsisBase SequenceEndodeoxyribonucleasesGene TargetingMolecular Sequence DataMultigene FamilyMutagenesis, Site-DirectedPlants, Genetically ModifiedZinc FingersEndodeoxyribonucleasesArabidopsisdeletioninversiontandemly arrayed genes (TAGs)zinc finger nuclease (ZFN)

Identifiers

PMID23979943
PMCPMC3789795
OpenAlexW2097433103

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.