Evidence map›Paper›PMID 34893590›Full record

ArticleNature communications2021

Exploiting a Y chromosome-linked Cas9 for sex selection and gene drive.

Stephanie Gamez, Duverney Chaverra-Rodriguez, Anna Buchman, Nikolay P Kandul, Stelia C Mendez-Sanchez, Jared B Bennett, Héctor M Sánchez C, Ting Yang, Igor Antoshechkin, Jonny E Duque and 3 more

Abstract 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 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
–field-weighted citation impact
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

14 citing papers in PubMed.

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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

13 authors.

Stephanie Gamez *Division of Biological Sciences, Section of Cell and Developmental Biology, University of California, San Diego, La Jolla, CA, 92093, USA.ORCID http://orcid.org/0000-0003-0665-0066
Duverney Chaverra-Rodriguez *Division of Biological Sciences, Section of Cell and Developmental Biology, University of California, San Diego, La Jolla, CA, 92093, USA.ORCID http://orcid.org/0000-0001-8068-7436
Anna BuchmanDivision of Biological Sciences, Section of Cell and Developmental Biology, University of California, San Diego, La Jolla, CA, 92093, USA.ORCID http://orcid.org/0000-0002-8775-6147
Nikolay P KandulDivision of Biological Sciences, Section of Cell and Developmental Biology, University of California, San Diego, La Jolla, CA, 92093, USA.
Stelia C Mendez-SanchezDivision of Biological Sciences, Section of Cell and Developmental Biology, University of California, San Diego, La Jolla, CA, 92093, USA.ORCID http://orcid.org/0000-0002-2402-3632
Jared B BennettBiophysics Graduate Group, University of California, Berkeley, CA, 94720, USA.ORCID http://orcid.org/0000-0003-4718-257X
Héctor M Sánchez CDivisions of Epidemiology & Biostatistics, School of Public Health, University of California, Berkeley, CA, 94720, USA.ORCID http://orcid.org/0000-0001-7378-8853
Ting YangDivision of Biological Sciences, Section of Cell and Developmental Biology, University of California, San Diego, La Jolla, CA, 92093, USA.ORCID http://orcid.org/0000-0001-7201-4231
Igor AntoshechkinDivision of Biology and Biological Engineering (BBE), California Institute of Technology, Pasadena, CA, 91125, USA.ORCID http://orcid.org/0000-0002-9934-3040
Jonny E DuqueDivision of Biological Sciences, Section of Cell and Developmental Biology, University of California, San Diego, La Jolla, CA, 92093, USA.ORCID http://orcid.org/0000-0003-2245-0558
Philippos A PapathanosDepartment of Entomology, Robert H. Smith Faculty of Agriculture, Food and Environment, Hebrew University of Jerusalem, Rehovot, 7610001, Israel.
John M MarshallDivisions of Epidemiology & Biostatistics, School of Public Health, University of California, Berkeley, CA, 94720, USA.ORCID http://orcid.org/0000-0003-0603-7341
Omar S AkbariDivision of Biological Sciences, Section of Cell and Developmental Biology, University of California, San Diego, La Jolla, CA, 92093, USA. oakbari@ucsd.edu.ORCID http://orcid.org/0000-0002-6853-9884

Funding

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
NIAID NIH HHS R01 AI151004
6 · The paper itself

Abstract

CRISPR-based genetic engineering tools aimed to bias sex ratios, or drive effector genes into animal populations, often integrate the transgenes into autosomal chromosomes. However, in species with heterogametic sex chromsomes (e.g. XY, ZW), sex linkage of endonucleases could be beneficial to drive the expression in a sex-specific manner to produce genetic sexing systems, sex ratio distorters, or even sex-specific gene drives, for example. To explore this possibility, here we develop a transgenic line of Drosophila melanogaster expressing Cas9 from the Y chromosome. We functionally characterize the utility of this strain for both sex selection and gene drive finding it to be quite effective. To explore its utility for population control, we built mathematical models illustrating its dynamics as compared to other state-of-the-art systems designed for both population modification and suppression. Taken together, our results contribute to the development of current CRISPR genetic control tools and demonstrate the utility of using sex-linked Cas9 strains for genetic control of animals.

Indexed as

CRISPR-Cas SystemsGenes, Y-LinkedY ChromosomeAnimalsAnimals, Genetically ModifiedDrosophila melanogasterEndonucleasesFemaleGene Drive TechnologyGene EditingMaleSex PreselectionSex RatioSynthetic BiologyTransgenesEndonucleases

Identifiers

PMID34893590
PMCPMC8664916

What OpenQuestion holds

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LicenceCC BY
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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.