Evidence map›Paper›PMID 27443923›Full record

ArticleMethods in cell biology2016

Precise genome editing by homologous recombination.

K Hoshijima, M J Jurynec, D J Grunwald

Open access · greenAbstract read
In one paragraph

Article in Methods in cell biology, 2016. 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
7.5field-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

14 citing papers in PubMed, 36 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Review
  5. Article
  6. Review
  7. Article
  8. Article
  9. Gene targeting in polymerase theta-deficient Arabidopsis thaliana.The Plant journal : for cell and molecular biology · 2022
    Article
  10. Article
  11. Article
  12. Article
  13. Review
  14. 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

3 authors at 1 institution in 1 country.

K HoshijimaUniversity of Utah, Salt Lake City, UT, United States.
M J JurynecUniversity of Utah, Salt Lake City, UT, United States.
D J GrunwaldUniversity of Utah, Salt Lake City, UT, United States.
University of Utah · US

Funding

UTAH REGIONAL CANCER CENTERP30CA042014 · NCI · UTAH STATE HIGHER EDUCATION SYSTEM--UNIVERSITY OF UTAH · PI CORNELIA M ULRICH · 1986 to 2026
$72.6M
TRAINING PROGRAM IN GENETICST32GM007464 · NIGMS · UNIVERSITY OF UTAH · PI GRUNWALD, DAVID J., STANFIELD, GILLIAN · 1985 to 2020
$6.1M
A Toolkit for Gene-Targeting in ZebrafishR01HD081950 · NICHD · UNIVERSITY OF UTAH · PI GRUNWALD, DAVID J. · 2014 to 2018
$2.0M
Gene targeting in zebrafish: building models to assay disease genesR21OD018323 · OD · UNIVERSITY OF UTAH · PI GRUNWALD, DAVID J. · 2014 to 2015
$406k
Gene Targeting by Homologous Recombination in the ZebrafishR21HD073847 · NICHD · UNIVERSITY OF UTAH · PI GRUNWALD, DAVID J. · 2012 to 2013
$401k
NCI NIH HHS P30 CA042014NICHD NIH HHS R01 HD081950NICHD NIH HHS R21 HD073847NIGMS NIH HHS T32 GM007464NIH HHS R21 OD018323
6 · The paper itself

Abstract

Simple and efficient methods are presented for creating precise modifications of the zebrafish genome. Edited alleles are generated by homologous recombination between the host genome and double-stranded DNA (dsDNA) donor molecules, stimulated by the induction of double-strand breaks at targeted loci in the host genome. Because several kilobase-long tracts of sequence can be exchanged, multiple genome modifications can be generated simultaneously at a single locus. Methods are described for creating: (1) alleles with simple sequence changes or in-frame additions, (2) knockin/knockout alleles that express a reporter protein from an endogenous locus, and (3) conditional alleles in which exons are flanked by recombinogenic loxP sites. Significantly, our approach to genome editing allows the incorporation of a linked reporter gene into the donor sequences so that successfully edited alleles can be identified by virtue of expression of the reporter. Factors affecting the efficiency of genome editing are discussed, including the finding that dsDNA products of I-SceI meganuclease enzyme digestion are particularly effective as donor molecules for gene-editing events. Reagents and procedures are described for accomplishing efficient genome editing in the zebrafish.

Indexed as

AnimalsDeoxyribonucleases, Type II Site-SpecificDNAGene EditingGene TargetingGenetic EngineeringGenomeHomologous RecombinationSaccharomyces cerevisiae ProteinsZebrafishAI4 protein, S cerevisiaeDeoxyribonucleases, Type II Site-SpecificDNASaccharomyces cerevisiae ProteinsConditional mutationGenome editingHomologous recombinationKnockin mutationZebrafish

Identifiers

PMID27443923
PMCPMC5127288
OpenAlexW2506112079

What OpenQuestion holds

Textmetadata
LicenceTDM
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.