Evidence map›Paper›PMID 34913119›Full record

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

Generating Zebrafish RNA-Less Mutant Alleles by Deleting Gene Promoters with CRISPR/Cas9.

Priyanka Kumari, Morgan Sturgeon, Gregory Bonde, Robert A Cornell

Abstract read
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 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Expanding the CRISPR/Cas toolkit: applications in proteomics and theranostics.Frontiers in bioengineering and biotechnology · 2025
    Review
  2. 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

4 authors.

Priyanka KumariDepartment of Anatomy and Cell Biology, University of Iowa, Iowa City, IA, USA.
Morgan SturgeonDepartment of Anatomy and Cell Biology, University of Iowa, Iowa City, IA, USA.
Gregory BondeDepartment of Anatomy and Cell Biology, University of Iowa, Iowa City, IA, USA.
Robert A CornellDepartment of Anatomy and Cell Biology, University of Iowa, Iowa City, IA, USA. robert-cornell@uiowa.edu.

Funding

Dissecting the transcriptional network governing differentiation of peridermR01DE023575 · NIDCR · UNIVERSITY OF WASHINGTON · PI CORNELL, ROBERT AARON, SCHUTTE, BRIAN C · 2013 to 2023
$4.3M
Transfer 5R01DE027983 - Genomic and Functional Analysis of IRF6 Target Genes in Orofacial Cleft PathogenesisR01DE027983 · NIDCR · MASSACHUSETTS GENERAL HOSPITAL · PI LIAO, ERIC CHIEN-WEI · 2019 to 2023
$3.3M
Genetic underpinnings of craniofacial disorders explored with spatial sequencingR01DE033016 · NIDCR · UNIVERSITY OF WASHINGTON · PI Robert Aaron Cornell, Julie Mathieu · 2023 to 2026
$2.9M
Functional tests of non-coding DNA variants associated with risk for orofacial clefting.R01DE027362 · NIDCR · UNIVERSITY OF WASHINGTON · PI CORNELL, ROBERT AARON · 2018 to 2022
$2.2M
NIDCR NIH HHS R01 DE023575NIDCR NIH HHS R01 DE027362NIDCR NIH HHS R01 DE027983NIDCR NIH HHS R01 DE033016
6 · The paper itself

Abstract

Danio rerio (zebrafish), traditionally used in forward genetic screens, has in the last decade become a popular model for reverse genetic studies with the introduction of TALENS, zinc finger nucleases, and CRISPR/Cas9. Unexpectedly, homozygous frameshift mutations generated by these tools frequently result in phenotypes that are less penetrant than those seen in embryos injected with antisense morpholino oligonucleotides targeting the same gene. One explanation for the difference is that some frameshift mutations result in nonsense-mediated decay of the gene transcript, a process which can induce expression of homologous genes. This form of genetic compensation, called transcriptional adaptation, does not occur when the mutant allele results in no RNA transcripts being produced from the targeted gene. Such RNA-less mutants can be generated by deleting a gene's promoter using a pair of guide RNAs and Cas9 protein. Here, we present a protocol and use it to generate alleles of arhgap29b and slc41a1 that lack detectable zygotic transcription. In the case of the arhgap29b mutant, an emerging phenotype did not segregate with the promoter deletion mutation, highlighting the potential for off-target mutagenesis with these tools. In summary, this chapter describes a method to generate zebrafish mutants that avoid a form of genetic compensation that occurs in many frameshift mutants.

Indexed as

ZebrafishAllelesAnimalsCation Transport ProteinsCRISPR-Cas SystemsRNARNA, Guide, CRISPR-Cas SystemsZebrafish ProteinsCation Transport ProteinsRNARNA, Guide, CRISPR-Cas SystemsSLC41A1 protein, zebrafishZebrafish Proteinsarhgap29bCRISPR/Cas9RNA-less mutantZebrafish

Identifiers

PMID34913119
PMCPMC10136374

What Socratic holds

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Registered trials

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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 Socratic graph.