Evidence map›Paper›PMID 36418866›Full record

ArticleNature communications2022

CRISPR-Cas12a induced DNA double-strand breaks are repaired by multiple pathways with different mutation profiles in Magnaporthe oryzae.

Jun Huang, David Rowe, Pratima Subedi, Wei Zhang, Tyler Suelter, Barbara Valent, David E Cook

Open access · goldAbstract read
In one paragraph

Article in Nature communications, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed
3.2field-weighted citation impact, top 7% 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

21 citing papers in PubMed, 39 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Genome editing in grain legumes for food security.Frontiers in genome editing · 2025
    Review
  8. Article
  9. Article
  10. Comparison of CRISPR-MAD7 and CRISPR-Cas9 for Gene Disruptions inJournal of fungi (Basel, Switzerland) · 2024
    Article
  11. Article
  12. Review
  13. Unanticipated Large-Scale Deletion inJournal of fungi (Basel, Switzerland) · 2023
    Article
  14. Article
  15. Review
  16. Review
  17. The Devastating Rice Blast Airborne PathogenPathogens (Basel, Switzerland) · 2023
    Review
  18. Article
  19. A Mad7 System for Genetic Engineering of Filamentous Fungi.Journal of fungi (Basel, Switzerland) · 2022
    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

7 authors at 1 institution in 1 country.

Jun HuangDepartment of Plant Pathology, Kansas State University, Manhattan, KS, 66506-5502, USA.ORCID 0000-0002-4071-0926
David RoweDepartment of Plant Pathology, Kansas State University, Manhattan, KS, 66506-5502, USA.
Pratima SubediDepartment of Plant Pathology, Kansas State University, Manhattan, KS, 66506-5502, USA.
Wei ZhangDepartment of Plant Pathology, Kansas State University, Manhattan, KS, 66506-5502, USA.
Tyler SuelterDepartment of Plant Pathology, Kansas State University, Manhattan, KS, 66506-5502, USA.
Barbara ValentDepartment of Plant Pathology, Kansas State University, Manhattan, KS, 66506-5502, USA.ORCID 0000-0002-5088-3345
David E CookDepartment of Plant Pathology, Kansas State University, Manhattan, KS, 66506-5502, USA. decook@ksu.edu.ORCID 0000-0002-2719-4701
Kansas State University · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

CRISPR-Cas mediated genome engineering has revolutionized functional genomics. However, understanding of DNA repair following Cas-mediated DNA cleavage remains incomplete. Using Cas12a ribonucleoprotein genome editing in the fungal pathogen, Magnaporthe oryzae, we detail non-canonical DNA repair outcomes from hundreds of transformants. Sanger and nanopore sequencing analysis reveals significant variation in DNA repair profiles, ranging from small INDELs to kilobase size deletions and insertions. Furthermore, we find the frequency of DNA repair outcomes varies between loci. The results are not specific to the Cas-nuclease or selection procedure. Through Ku80 deletion analysis, a key protein required for canonical non-homologous end joining, we demonstrate activity of an alternative end joining mechanism that creates larger DNA deletions, and uses longer microhomology compared to C-NHEJ. Together, our results suggest preferential DNA repair pathway activity in the genome that can create different mutation profiles following repair, which could create biased genome variation and impact genome engineering and genome evolution.

Indexed as

CRISPR-Cas SystemsDNA Breaks, Double-StrandedAscomycotaDNAMutationDNA

Identifiers

PMID36418866
PMCPMC9684475
OpenAlexW4309745565

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.