Evidence map›Paper›PMID 26269544›Full record

ArticlePlant physiology2015

Targeted Mutagenesis, Precise Gene Editing, and Site-Specific Gene Insertion in Maize Using Cas9 and Guide RNA.

Sergei Svitashev, Joshua K Young, Christine Schwartz, Huirong Gao, S Carl Falco, A Mark Cigan

Abstract read
In one paragraph

Article in Plant physiology, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 315 papers.

0numbers the graph read from it
0cells of the map it votes in
315citing 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

315 citing papers in PubMed.

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  7. Targeted knockout of a host peroxisomal peptidase confers field resistance to maize lethal necrosis.Proceedings of the National Academy of Sciences of the United States of America · 2026
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  16. The Role ofInternational journal of molecular sciences · 2025
    Review
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255 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

6 authors.

Sergei SvitashevTrait Enabling Technologies, DuPont Pioneer, Johnston, Iowa 50131 mark.cigan@pioneer.com.ORCID http://orcid.org/0000-0002-5926-3839
Joshua K YoungTrait Enabling Technologies, DuPont Pioneer, Johnston, Iowa 50131 mark.cigan@pioneer.com.
Christine SchwartzTrait Enabling Technologies, DuPont Pioneer, Johnston, Iowa 50131.
Huirong GaoTrait Enabling Technologies, DuPont Pioneer, Johnston, Iowa 50131.
S Carl FalcoTrait Enabling Technologies, DuPont Pioneer, Johnston, Iowa 50131.
A Mark CiganTrait Enabling Technologies, DuPont Pioneer, Johnston, Iowa 50131 mark.cigan@pioneer.com.ORCID http://orcid.org/0000-0002-5983-5235

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Targeted mutagenesis, editing of endogenous maize (Zea mays) genes, and site-specific insertion of a trait gene using clustered regularly interspaced short palindromic repeats (CRISPR)-associated (Cas)-guide RNA technology are reported in maize. DNA vectors expressing maize codon-optimized Streptococcus pyogenes Cas9 endonuclease and single guide RNAs were cointroduced with or without DNA repair templates into maize immature embryos by biolistic transformation targeting five different genomic regions: upstream of the liguleless1 (LIG1) gene, male fertility genes (Ms26 and Ms45), and acetolactate synthase (ALS) genes (ALS1 and ALS2). Mutations were subsequently identified at all sites targeted, and plants containing biallelic multiplex mutations at LIG1, Ms26, and Ms45 were recovered. Biolistic delivery of guide RNAs (as RNA molecules) directly into immature embryo cells containing preintegrated Cas9 also resulted in targeted mutations. Editing the ALS2 gene using either single-stranded oligonucleotides or double-stranded DNA vectors as repair templates yielded chlorsulfuron-resistant plants. Double-strand breaks generated by RNA-guided Cas9 endonuclease also stimulated insertion of a trait gene at a site near LIG1 by homology-directed repair. Progeny showed expected Mendelian segregation of mutations, edits, and targeted gene insertions. The examples reported in this study demonstrate the utility of Cas9-guide RNA technology as a plant genome editing tool to enhance plant breeding and crop research needed to meet growing agriculture demands of the future.

Indexed as

Clustered Regularly Interspaced Short Palindromic RepeatsRNA, Guide, CRISPR-Cas SystemsAcetolactate SynthaseAgrobacteriumAmino Acid SequenceGene Knockout TechniquesGenetic EngineeringMolecular Sequence DataMutagenesis, InsertionalMutationPlant BreedingPlant ProteinsZea maysAcetolactate SynthasePlant ProteinsRNA, Guide, CRISPR-Cas Systems

Identifiers

PMID26269544
PMCPMC4587463

What OpenQuestion holds

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Registered trials

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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.