Evidence map›Paper›PMID 35180218›Full record

ArticlePLoS genetics2022

Considerations for homology-based DNA repair in mosquitoes: Impact of sequence heterology and donor template source.

Joshua Xin De Ang, Katherine Nevard, Rebekah Ireland, Deepak-Kumar Purusothaman, Sebald A N Verkuijl, Lewis Shackleford, Estela Gonzalez, Michelle A E Anderson, Luke Alphey

Open access · goldAbstract read
In one paragraph

Article in PLoS genetics, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
1.2field-weighted citation impact, top 23% 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

10 citing papers in PubMed, 15 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Review
  10. 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

9 authors at 1 institution in 1 country.

Joshua Xin De AngThe Pirbright Institute, Pirbright, Woking, United Kingdom.ORCID 0000-0002-4710-8831
Katherine NevardThe Pirbright Institute, Pirbright, Woking, United Kingdom.ORCID 0000-0002-1008-6587
Rebekah IrelandThe Pirbright Institute, Pirbright, Woking, United Kingdom.
Deepak-Kumar PurusothamanThe Pirbright Institute, Pirbright, Woking, United Kingdom.ORCID 0000-0003-4827-6519
Sebald A N VerkuijlThe Pirbright Institute, Pirbright, Woking, United Kingdom.ORCID 0000-0002-6771-0280
Lewis ShacklefordThe Pirbright Institute, Pirbright, Woking, United Kingdom.ORCID 0000-0002-8154-5154
Estela GonzalezThe Pirbright Institute, Pirbright, Woking, United Kingdom.ORCID 0000-0002-4296-0080
Michelle A E AndersonThe Pirbright Institute, Pirbright, Woking, United Kingdom.ORCID 0000-0003-1510-2942
Luke AlpheyThe Pirbright Institute, Pirbright, Woking, United Kingdom.ORCID 0000-0002-2916-3802
The Pirbright Institute · GB

Funding

Biotechnology and Biological Sciences Research Council BBS/E/I/00007033Biotechnology and Biological Sciences Research Council BBS/E/I/00007038Biotechnology and Biological Sciences Research Council BBS/E/I/00007039
6 · The paper itself

Abstract

The increasing prevalence of insecticide resistance and the ongoing global burden of vector-borne diseases have encouraged new efforts in mosquito control. For Aedes aegypti, the most important arboviral vector, integration rates achieved in Cas9-based knock-ins so far have been rather low, highlighting the need to understand gene conversion patterns and other factors that influence homology-directed repair (HDR) events in this species. In this study, we report the effects of sequence mismatches or donor template forms on integration rates. We found that modest sequence differences between construct homology arms [DNA sequence in the donor template which resembles the region flanking the target cut] and genomic target comprising 1.2% nucleotide dissimilarity (heterology) significantly reduced integration rates. While most integrations (59-88%) from plasmid templates were the result of canonical [on target, perfect repair] HDR events, no canonical events were identified from other donor types (i.e. ssDNA, biotinylated ds/ssDNA). Sequencing of the transgene flanking region in 69 individuals with canonical integrations revealed 60% of conversion tracts to be unidirectional and extend up to 220 bp proximal to the break, though in three individuals bidirectional conversion of up to 725 bp was observed.

Indexed as

CRISPR-Cas SystemsCulicidaeAnimalsDNA RepairGenomeHumansMosquito Vectors

Identifiers

PMID35180218
PMCPMC8893643
OpenAlexW4213081408

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.