Evidence map›Paper›PMID 28195201›Full record

ArticleScientific reports2017

CRISPR/Cas9-mediated genome editing in wild-derived mice: generation of tamed wild-derived strains by mutation of the a (nonagouti) gene.

Michiko Hirose, Ayumi Hasegawa, Keiji Mochida, Shogo Matoba, Yuki Hatanaka, Kimiko Inoue, Tatsuhiko Goto, Hideki Kaneda, Ikuko Yamada, Tamio Furuse and 6 more

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
0.9field-weighted citation impact, top 27% 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

7 citing papers in PubMed, 20 citations in OpenAlex.

  1. Article
  2. Article
  3. Mammalian genome research resources available from the National BioResource Project in Japan.Mammalian genome : official journal of the International Mammalian Genome Society · 2024
    Review
  4. Article
  5. Article
  6. Article
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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

16 authors at 5 institutions in 1 country.

Michiko HiroseRIKEN BioResource Center, Tsukuba, Ibaraki 305-0074, Japan.
Ayumi HasegawaRIKEN BioResource Center, Tsukuba, Ibaraki 305-0074, Japan.
Keiji MochidaRIKEN BioResource Center, Tsukuba, Ibaraki 305-0074, Japan.
Shogo MatobaRIKEN BioResource Center, Tsukuba, Ibaraki 305-0074, Japan.
Yuki HatanakaRIKEN BioResource Center, Tsukuba, Ibaraki 305-0074, Japan.
Kimiko InoueRIKEN BioResource Center, Tsukuba, Ibaraki 305-0074, Japan.
Tatsuhiko GotoDepartment of Biological Production Science, College of Agriculture, Ibaraki University, Ami, Ibaraki 300-0393, Japan.
Hideki KanedaRIKEN BioResource Center, Tsukuba, Ibaraki 305-0074, Japan.
Ikuko YamadaRIKEN BioResource Center, Tsukuba, Ibaraki 305-0074, Japan.
Tamio FuruseRIKEN BioResource Center, Tsukuba, Ibaraki 305-0074, Japan.
Kuniya AbeRIKEN BioResource Center, Tsukuba, Ibaraki 305-0074, Japan.
Yoshihisa UenoyamaGraduate School of Bioagricultural Sciences, Nagoya University, Nagoya, Aichi 464-8601, Japan.
Hiroko TsukamuraGraduate School of Bioagricultural Sciences, Nagoya University, Nagoya, Aichi 464-8601, Japan.
Shigeharu WakanaRIKEN BioResource Center, Tsukuba, Ibaraki 305-0074, Japan.
Arata HondaRIKEN BioResource Center, Tsukuba, Ibaraki 305-0074, Japan.
Atsuo OguraRIKEN BioResource Center, Tsukuba, Ibaraki 305-0074, Japan.
RIKEN BioResource Research Center · JPNagoya University · JPIbaraki University · JPUniversity of Miyazaki · JPUniversity of Tsukuba · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Wild-derived mice have contributed to experimental mouse genetics by virtue of their genetic diversity, which may help increase the chance of identifying novel modifier genes responsible for specific phenotypes and diseases. However, gene targeting using wild-derived mice has been unsuccessful because of the unavailability of stable embryonic stem cells. Here, we report that CRISPR/Cas9-mediated gene targeting can be applied to the Japanese wild-derived MSM/Ms strain (Mus musculus molossinus). We targeted the nonagouti (a) gene encoding the agouti protein that is localized in hair and the brain. We obtained three homozygous knockout mice as founders, all showing black coat colour. While homozygous knockout offspring were physiologically indistinguishable from wild-type litter-mates, they showed specific domesticated behaviours: hypoactivity in the dark phase and a decline in the avoidance of a human hand. These phenotypes were consistent over subsequent generations. Our findings support the empirical hypothesis that nonagouti is a domestication-linked gene, the loss of which might repress aggressive behaviour.

Indexed as

CRISPR-Cas SystemsGene EditingAgouti Signaling ProteinAllelesAnimalsAnimals, WildDNA Mutational AnalysisDopamineGene ExpressionHumansMesencephalonMiceMice, KnockoutMutationPhenotypeAgouti Signaling Proteina protein, mouseDopamine

Identifiers

PMID28195201
PMCPMC5307340
OpenAlexW2588029483

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.