Evidence map›Paper›PMID 35696035›Full record

ArticleMethods in molecular biology (Clifton, N.J.)2022

Generation of Gene Drive Mice for Invasive Pest Population Suppression.

Mark D Bunting, Chandran Pfitzner, Luke Gierus, Melissa White, Sandra Piltz, Paul Q Thomas

Abstract read
PubMed Publisher
In one paragraph

Article in Methods in molecular biology (Clifton, N.J.), 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
3.5field-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

5 citing papers in PubMed, 8 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Leveraging a natural murine meiotic drive to suppress invasive populations.Proceedings of the National Academy of Sciences of the United States of America · 2022
    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

6 authors at 2 institutions in 1 country.

Mark D BuntingSchool of Medicine, University of Adelaide, North Terrace, Adelaide, SA, Australia.
Chandran PfitznerSchool of Medicine, University of Adelaide, North Terrace, Adelaide, SA, Australia.
Luke GierusSchool of Medicine, University of Adelaide, North Terrace, Adelaide, SA, Australia.
Melissa WhiteSchool of Medicine, University of Adelaide, North Terrace, Adelaide, SA, Australia.
Sandra PiltzSchool of Medicine, University of Adelaide, North Terrace, Adelaide, SA, Australia.
Paul Q ThomasSchool of Medicine, University of Adelaide, North Terrace, Adelaide, SA, Australia. paul.thomas@adelaide.edu.au.
University of Adelaide · AUAustralian Genome Research Facility · AU

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Gene drives are genetic elements that are transmitted to greater than 50% of offspring and have potential for population modification or suppression. While gene drives are known to occur naturally, the recent emergence of CRISPR-Cas9 genome-editing technology has enabled generation of synthetic gene drives in a range of organisms including mosquitos, flies, and yeast. For example, studies in Anopheles mosquitos have demonstrated >95% transmission of CRISPR-engineered gene drive constructs, providing a possible strategy for malaria control. Recently published studies have also indicated that it may be possible to develop gene drive technology in invasive rodents such as mice. Here, we discuss the prospects for gene drive development in mice, including synthetic "homing drive" and X-shredder strategies as well as modifications of the naturally occurring t haplotype. We also provide detailed protocols for generation of gene drive mice through incorporation of plasmid-based transgenes in a targeted and non-targeted manner. Importantly, these protocols can be used for generating transgenic mice for any project that requires insertion of kilobase-scale transgenes such as knock-in of fluorescent reporters, gene swaps, overexpression/ectopic expression studies, and conditional "floxed" alleles.

Indexed as

Gene Drive TechnologyAnimalsCRISPR-Cas SystemsGene EditingIntroduced SpeciesMiceMice, TransgenicTransgenesCRISPRGene driveGenetic biocontrolGenome editingMouse models

Identifiers

PMID35696035
OpenAlexW4285226724

What OpenQuestion holds

Textmetadata
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.