Evidence map›Paper›PMID 33674604›Full record

ArticleNature communications2021

Inherently confinable split-drive systems in Drosophila.

Gerard Terradas, Anna B Buchman, Jared B Bennett, Isaiah Shriner, John M Marshall, Omar S Akbari, Ethan Bier

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 48 papers.

0numbers the graph read from it
0cells of the map it votes in
48citing papers in PubMed
6.1field-weighted citation impact, top 2% 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

48 citing papers in PubMed, 93 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Review
  6. Article
  7. Article
  8. Article
  9. Review
  10. Review
  11. Article
  12. Article
  13. Article
  14. Review
  15. Article
  16. Article
  17. Article
  18. Article
  19. Article
  20. 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

7 authors at 3 institutions in 1 country.

Gerard TerradasSection of Cell and Developmental Biology, University of California, San Diego, La Jolla, CA, USA.ORCID 0000-0003-4285-4007
Anna B BuchmanSection of Cell and Developmental Biology, University of California, San Diego, La Jolla, CA, USA.
Jared B BennettBiophysics Graduate Group, Division of Biological Sciences, College of Letters and Science, University of California, Berkeley, CA, USA.ORCID 0000-0003-4718-257X
Isaiah ShrinerSection of Cell and Developmental Biology, University of California, San Diego, La Jolla, CA, USA.
John M MarshallDivisions of Epidemiology and Biostatistics, School of Public Health, University of California, Berkeley, CA, USA.ORCID 0000-0003-0603-7341
Omar S AkbariSection of Cell and Developmental Biology, University of California, San Diego, La Jolla, CA, USA.ORCID 0000-0002-6853-9884
Ethan BierSection of Cell and Developmental Biology, University of California, San Diego, La Jolla, CA, USA. ebier@ucsd.edu.ORCID 0000-0002-2892-3005
University of California San Diego · USBerkeley College · USInnovative Genomics Institute · US

Funding

The mutagenic chain reaction: a method for autocatalyic gene disseminationR01GM117321 · NIGMS · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI BIER, ETHAN · 2016 to 2024
$2.5M
Development of synthetic viral circuitry to regulate viruses in mosquito disease vectorsDP2AI152071 · NIAID · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI AKBARI, OMAR SULTAN · 2019 to 2019
$2.4M
Precision guided SIT for the control of vector-borne diseaseR01AI151004 · NIAID · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI AKBARI, OMAR SULTAN · 2020 to 2024
$2.3M
Transcriptome engineering technologies for the development of antiviral effectors in mosquitoesR21AI149161 · NIAID · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI AKBARI, OMAR SULTAN · 2020 to 2021
$434k
NIAID NIH HHS DP2 AI152071NIAID NIH HHS R01 AI151004NIAID NIH HHS R21 AI149161NIGMS NIH HHS R01 GM117321
6 · The paper itself

Abstract

CRISPR-based gene-drive systems, which copy themselves via gene conversion mediated by the homology-directed repair (HDR) pathway, have the potential to revolutionize vector control. However, mutant alleles generated by the competing non-homologous end-joining (NHEJ) pathway, resistant to Cas9 cleavage, can interrupt the spread of gene-drive elements. We hypothesized that drives targeting genes essential for viability or reproduction also carrying recoded sequences that restore endogenous gene functionality should benefit from dominantly-acting maternal clearance of NHEJ alleles combined with recessive Mendelian culling processes. Here, we test split gene-drive (sGD) systems in Drosophila melanogaster that are inserted into essential genes required for viability (rab5, rab11, prosalpha2) or fertility (spo11). In single generation crosses, sGDs copy with variable efficiencies and display sex-biased transmission. In multigenerational cage trials, sGDs follow distinct drive trajectories reflecting their differential tendencies to induce target chromosome damage and/or lethal/sterile mosaic Cas9-dependent phenotypes, leading to inherently confinable drive outcomes.

Indexed as

AllelesAnimalsAnimals, Genetically ModifiedClustered Regularly Interspaced Short Palindromic RepeatsCRISPR-Cas SystemsDNA End-Joining RepairDrosophilaDrosophila melanogasterFemaleGene Drive TechnologyGene EditingMaleRecombinational DNA Repair

Identifiers

PMID33674604
PMCPMC7935863
OpenAlexW3135419966

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.