Evidence map›Paper›PMID 27053096›Full record

ArticleExperimental animals2016

Generation of CRISPR/Cas9-mediated bicistronic knock-in ins1-cre driver mice.

Yoshikazu Hasegawa, Yoshikazu Hoshino, Abdelaziz E Ibrahim, Kanako Kato, Yoko Daitoku, Yoko Tanimoto, Yoshihisa Ikeda, Hisashi Oishi, Satoru Takahashi, Atsushi Yoshiki and 4 more

Open access · diamondAbstract read
In one paragraph

Article in Experimental animals, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
2.8field-weighted citation impact, top 10% 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

19 citing papers in PubMed, 26 citations in OpenAlex.

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  16. Gene-edited CRISPy Critters for alcohol research.Alcohol (Fayetteville, N.Y.) · 2019
    Review
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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

14 authors at 4 institutions in 2 countries.

Yoshikazu HasegawaLaborarory Animal Resource Center, University of Tsukuba, 1-1-1 Tennodai, Tsukuba, Ibaraki 305-8575, Japan.
Yoshikazu Hoshino
Abdelaziz E Ibrahim
Kanako Kato
Yoko Daitoku
Yoko Tanimoto
Yoshihisa Ikeda
Hisashi Oishi
Satoru Takahashi
Atsushi Yoshiki
Ken-Ichi Yagami
Hiroyoshi Iseki
Seiya Mizuno
Fumihiro Sugiyama
University of Tsukuba · JPRIKEN BioResource Research Center · JPSuez Canal University · EGTsukuba International University · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

In the present study, we generated novel cre driver mice for gene manipulation in pancreatic β cells. Using the CRISPR/Cas9 system, stop codon sequences of Ins1 were targeted for insertion of cre, including 2A sequences. A founder of C57BL/6J-Ins1(em1 (cre) Utr) strain was produced from an oocyte injected with pX330 containing the sequences encoding gRNA and Cas9 and a DNA donor plasmid carrying 2A-cre. (R26GRR x C57BL/6J-Ins1(em1 (cre) Utr)) F1 mice were histologically characterized for cre-loxP recombination in the embryonic and adult stages; cre-loxP recombination was observed in all pancreatic islets examined in which almost all insulin-positive cells showed tdsRed fluorescence, suggesting β cell-specific recombination. Furthermore, there were no significant differences in results of glucose tolerance test among genotypes (homo/hetero/wild). Taken together, these observations indicated that C57BL/6J-Ins1(em1 (cre) Utr) is useful for studies of glucose metabolism and the strategy of bicistronic cre knock-in using the CRISPR/Cas9 system could be useful for production of cre driver mice.

Indexed as

CRISPR-Cas SystemsInsulin-Secreting CellsMice, Mutant StrainsAnimalsCodon, TerminatorCrk-Associated Substrate ProteinGene EditingGlucoseInjectionsInsulinIntegrasesMice, Inbred C57BLMutagenesis, InsertionalOocytesRecombination, GeneticRNABcar1 protein, mouseCodon, TerminatorCre recombinaseCrk-Associated Substrate ProteinGlucoseIns1 protein, mouseInsulinIntegrasesRNA

Identifiers

PMID27053096
PMCPMC4976246
OpenAlexW2314187353

What OpenQuestion holds

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LicenceCC BY-NC-ND
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.