Evidence map›Paper›PMID 34799578›Full record

ArticleNature communications2021

Mechanistic and genetic basis of single-strand templated repair at Cas12a-induced DNA breaks in Chlamydomonas reinhardtii.

Aron Ferenczi, Yen Peng Chew, Erika Kroll, Charlotte von Koppenfels, Andrew Hudson, Attila Molnar

Open access · goldAbstract read
In one paragraph

Article in Nature communications, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
1.9field-weighted citation impact, top 14% 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

16 citing papers in PubMed, 35 citations in OpenAlex.

  1. Gene Editing inBio-protocol · 2026
    Article
  2. Article
  3. CRISPR-Cas Technology TurnsMarine drugs · 2025
    Review
  4. Article
  5. Article
  6. Manipulating alternative end-joining alters carbon-ion beam-induced genome mutation profiles in Arabidopsis thaliana.DNA research : an international journal for rapid publication of reports on genes and genomes · 2025
    Article
  7. Article
  8. Review
  9. Article
  10. Review
  11. Article
  12. Review
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  14. Article
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  16. Review
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 at 2 institutions in 1 country.

Aron FerencziInstitute of Molecular Plant Sciences, University of Edinburgh, Edinburgh, EH9 3BF, UK.ORCID http://orcid.org/0000-0002-2100-1702
Yen Peng ChewInstitute of Molecular Plant Sciences, University of Edinburgh, Edinburgh, EH9 3BF, UK.
Erika KrollInstitute of Molecular Plant Sciences, University of Edinburgh, Edinburgh, EH9 3BF, UK.ORCID http://orcid.org/0000-0001-8832-7208
Charlotte von KoppenfelsInstitute of Molecular Plant Sciences, University of Edinburgh, Edinburgh, EH9 3BF, UK.
Andrew HudsonInstitute of Molecular Plant Sciences, University of Edinburgh, Edinburgh, EH9 3BF, UK.ORCID http://orcid.org/0000-0001-9049-0100
Attila MolnarInstitute of Molecular Plant Sciences, University of Edinburgh, Edinburgh, EH9 3BF, UK. attila.molnar@ed.ac.uk.ORCID http://orcid.org/0000-0002-1044-6327
University of Edinburgh · GBRothamsted Research · GB

Funding

Biotechnology and Biological Sciences Research Council BB/R506163/1Biotechnology and Biological Sciences Research Council BB/V509188/1Biotechnology and Biological Sciences Research Council PHYCIBSC-03
6 · The paper itself

Abstract

Single-stranded oligodeoxynucleotides (ssODNs) are widely used as DNA repair templates in CRISPR/Cas precision genome editing. However, the underlying mechanisms of single-strand templated DNA repair (SSTR) are inadequately understood, constraining rational improvements to precision editing. Here we study SSTR at CRISPR/Cas12a-induced DNA double-strand breaks (DSBs) in the eukaryotic model green microalga Chlamydomonas reinhardtii. We demonstrate that ssODNs physically incorporate into the genome during SSTR at Cas12a-induced DSBs. This process is genetically independent of the Rad51-dependent homologous recombination and Fanconi anemia pathways, is strongly antagonized by non-homologous end-joining, and is mediated almost entirely by the alternative end-joining enzyme polymerase θ. These findings suggest differences in SSTR between C. reinhardtii and animals. Our work illustrates the promising potentially of C. reinhardtii as a model organism for studying nuclear DNA repair.

Indexed as

DNA End-Joining RepairBacterial ProteinsChlamydomonas reinhardtiiCRISPR-Associated ProteinsCRISPR-Cas SystemsDNA Breaks, Double-StrandedDNA-Directed DNA PolymeraseDNA, PlantDNA Polymerase thetaDNA, Single-StrandedEndodeoxyribonucleasesGene EditingGenomic InstabilityOligodeoxyribonucleotidesRNA, Guide, CRISPR-Cas SystemsBacterial ProteinsCas12a proteinCRISPR-Associated ProteinsDNA-Directed DNA PolymeraseDNA, PlantDNA Polymerase thetaDNA, Single-StrandedEndodeoxyribonucleasesOligodeoxyribonucleotidesRNA, Guide, CRISPR-Cas Systems

Identifiers

PMID34799578
PMCPMC8604939
OpenAlexW3211125905

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.