Evidence map›Paper›PMID 27855195›Full record

ArticlePloS one2016

Paternal Aging Affects Behavior in Pax6 Mutant Mice: A Gene/Environment Interaction in Understanding Neurodevelopmental Disorders.

Kaichi Yoshizaki, Tamio Furuse, Ryuichi Kimura, Valter Tucci, Hideki Kaneda, Shigeharu Wakana, Noriko Osumi

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed
1.8field-weighted citation impact, top 15% 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

20 citing papers in PubMed, 41 citations in OpenAlex.

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  8. Article
  9. The Role of Advanced Parental Age in Reproductive Genetics.Reproductive sciences (Thousand Oaks, Calif.) · 2023
    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

7 authors at 3 institutions in 2 countries.

Kaichi YoshizakiDepartment of Developmental Neuroscience, Tohoku University Graduate School of Medicine, Sendai, Miyagi, Japan.
Tamio FuruseTechnology and Development Team for Mouse Phenotype Analysis, The Japan Mouse Clinic, RIKEN BRC, Tsukuba, Ibaraki, Japan.
Ryuichi KimuraDepartment of Developmental Neuroscience, Tohoku University Graduate School of Medicine, Sendai, Miyagi, Japan.
Valter TucciDepartment of Neuroscience and Brain Technologies. Istituto Italiano di Tecnologia, Genova, Italy.
Hideki KanedaTechnology and Development Team for Mouse Phenotype Analysis, The Japan Mouse Clinic, RIKEN BRC, Tsukuba, Ibaraki, Japan.
Shigeharu WakanaTechnology and Development Team for Mouse Phenotype Analysis, The Japan Mouse Clinic, RIKEN BRC, Tsukuba, Ibaraki, Japan.
Noriko OsumiDepartment of Developmental Neuroscience, Tohoku University Graduate School of Medicine, Sendai, Miyagi, Japan.
RIKEN BioResource Research Center · JPTohoku University · JPItalian Institute of Technology · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Neurodevelopmental disorders such as autism spectrum disorder (ASD) and attention deficit and hyperactivity disorder (ADHD) have increased over the last few decades. These neurodevelopmental disorders are characterized by a complex etiology, which involves multiple genes and gene-environmental interactions. Various genes that control specific properties of neural development exert pivotal roles in the occurrence and severity of phenotypes associated with neurodevelopmental disorders. Moreover, paternal aging has been reported as one of the factors that contribute to the risk of ASD and ADHD. Here we report, for the first time, that paternal aging has profound effects on the onset of behavioral abnormalities in mice carrying a mutation of Pax6, a gene with neurodevelopmental regulatory functions. We adopted an in vitro fertilization approach to restrict the influence of additional factors. Comprehensive behavioral analyses were performed in Sey/+ mice (i.e., Pax6 mutant heterozygotes) born from in vitro fertilization of sperm taken from young or aged Sey/+ fathers. No body weight changes were found in the four groups, i.e., Sey/+ and wild type (WT) mice born to young or aged father. However, we found important differences in maternal separation-induced ultrasonic vocalizations of Sey/+ mice born from young father and in the level of hyperactivity of Sey/+ mice born from aged fathers in the open-field test, respectively, compared to WT littermates. Phenotypes of anxiety were observed in both genotypes born from aged fathers compared with those born from young fathers. No significant difference was found in social behavior and sensorimotor gating among the four groups. These results indicate that mice with a single genetic risk factor can develop different phenotypes depending on the paternal age. Our study advocates for serious considerations on the role of paternal aging in breeding strategies for animal studies.

Indexed as

Behavior, AnimalGene-Environment InteractionAffectAgingAnimalsAnxietyFearFemaleLocomotionMaleMemoryMice, Inbred C57BLMice, Mutant StrainsNeurodevelopmental DisordersPaternal AgePAX6 Transcription FactorPax6 protein, mousePAX6 Transcription Factor

Identifiers

PMID27855195
PMCPMC5113965
OpenAlexW2551912255

What OpenQuestion holds

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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.