Literature DB >> 32573780

Maternal approach behaviors toward neonatal calls are impaired by mother's experiences of raising pups with a risk gene variant for autism.

Risa Kato1, Akihiro Machida1, Kensaku Nomoto1, Gina Kang2, Takeshi Hiramoto2, Kenji Tanigaki3, Kazutaka Mogi1,4, Noboru Hiroi2,5,6,7, Takefumi Kikusui1,4.   

Abstract

How the intrinsic sequence structure of neonatal mouse pup ultrasonic vocalization (USV) and maternal experiences determine maternal behaviors in mice is poorly understood. Our previous work showed that pups with a Tbx1 heterozygous (HT) mutation, a genetic risk for autism spectrum disorder (ASD), emit altered call sequences that do not induce maternal approach behaviors in C57BL6/J mothers. Here, we tested how maternal approach behaviors induced by wild-type and HT USVs are influenced by the mother's experience in raising pups of these two genotypes. The results showed that wild-type USVs were effective in inducing maternal approach behaviors when mothers raised wild-type but not HT pups. The USVs of HT pups were ineffective regardless of whether mothers raised HT or wild-type pups. However, the sequence structure of pup USVs had no effect on the general, non-directional incentive motivation of maternal behaviors. Our data show how the mother's experience with a pup with a genetic risk for ASD alters the intrinsic incentive values of USV sequences in maternal approach behaviors.
© 2020 Wiley Periodicals LLC.

Entities:  

Keywords:  22q11; ASD; CNV; Tbx1; USV; maternal behaviors; mouse

Mesh:

Year:  2020        PMID: 32573780      PMCID: PMC7755688          DOI: 10.1002/dev.22006

Source DB:  PubMed          Journal:  Dev Psychobiol        ISSN: 0012-1630            Impact factor:   3.038


  28 in total

1.  Tbx1 haploinsufficiency is linked to behavioral disorders in mice and humans: implications for 22q11 deletion syndrome.

Authors:  Richard Paylor; Beate Glaser; Annalisa Mupo; Paris Ataliotis; Corinne Spencer; Angela Sobotka; Chelsey Sparks; Chul-Hee Choi; John Oghalai; Sarah Curran; Kieran C Murphy; Stephen Monks; Nigel Williams; Michael C O'Donovan; Michael J Owen; Peter J Scambler; Elizabeth Lindsay
Journal:  Proc Natl Acad Sci U S A       Date:  2006-05-09       Impact factor: 11.205

2.  Autism spectrum disorders and symptoms in children with molecularly confirmed 22q11.2 deletion syndrome.

Authors:  Sarah E Fine; Alison Weissman; Marsha Gerdes; Jennifer Pinto-Martin; Elaine H Zackai; Donna M McDonald-McGinn; Beverly S Emanuel
Journal:  J Autism Dev Disord       Date:  2005-08

3.  Mutation analysis of TBX1 in non-deleted patients with features of DGS/VCFS or isolated cardiovascular defects.

Authors:  W Gong; S Gottlieb; J Collins; A Blescia; H Dietz; E Goldmuntz; D M McDonald-McGinn; E H Zackai; B S Emanuel; D A Driscoll; M L Budarf
Journal:  J Med Genet       Date:  2001-12       Impact factor: 6.318

4.  Chromosome 22q11 deletion syndrome (CATCH 22): neuropsychiatric and neuropsychological aspects.

Authors:  Lena Niklasson; Peder Rasmussen; Sólveig Oskarsdóttir; Christopher Gillberg
Journal:  Dev Med Child Neurol       Date:  2002-01       Impact factor: 5.449

5.  Tbx1: identification of a 22q11.2 gene as a risk factor for autism spectrum disorder in a mouse model.

Authors:  Takeshi Hiramoto; Gina Kang; Go Suzuki; Yasushi Satoh; Raju Kucherlapati; Yasuhiro Watanabe; Noboru Hiroi
Journal:  Hum Mol Genet       Date:  2011-09-09       Impact factor: 6.150

6.  A role for maternal physiological state in preserving auditory cortical plasticity for salient infant calls.

Authors:  F G Lin; E E Galindo-Leon; T N Ivanova; R C Mappus; R C Liu
Journal:  Neuroscience       Date:  2013-05-21       Impact factor: 3.590

7.  Comparing phenotypes in patients with idiopathic autism to patients with velocardiofacial syndrome (22q11 DS) with and without autism.

Authors:  Wendy R Kates; Kevin M Antshel; Wanda P Fremont; Robert J Shprintzen; Leslie A Strunge; Courtney P Burnette; Anne Marie Higgins
Journal:  Am J Med Genet A       Date:  2007-11-15       Impact factor: 2.802

8.  TBX1 mutation identified by exome sequencing in a Japanese family with 22q11.2 deletion syndrome-like craniofacial features and hypocalcemia.

Authors:  Tsutomu Ogata; Tetsuya Niihori; Noriko Tanaka; Masahiko Kawai; Takeshi Nagashima; Ryo Funayama; Keiko Nakayama; Shinichi Nakashima; Fumiko Kato; Maki Fukami; Yoko Aoki; Yoichi Matsubara
Journal:  PLoS One       Date:  2014-03-17       Impact factor: 3.240

9.  Modeling and Predicting Developmental Trajectories of Neuropsychiatric Dimensions Associated With Copy Number Variations.

Authors:  Noboru Hiroi; Takahira Yamauchi
Journal:  Int J Neuropsychopharmacol       Date:  2019-08-01       Impact factor: 5.176

10.  Structure and function of neonatal social communication in a genetic mouse model of autism.

Authors:  T Takahashi; S Okabe; P Ó Broin; A Nishi; K Ye; M V Beckert; T Izumi; A Machida; G Kang; S Abe; J L Pena; A Golden; T Kikusui; N Hiroi
Journal:  Mol Psychiatry       Date:  2015-12-15       Impact factor: 15.992

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  3 in total

1.  Heterozygosity of murine Crkl does not recapitulate behavioral dimensions of human 22q11.2 hemizygosity.

Authors:  Takahira Yamauchi; Gina Kang; Noboru Hiroi
Journal:  Genes Brain Behav       Date:  2020-12-10       Impact factor: 3.449

2.  Tbx1, a gene encoded in 22q11.2 copy number variant, is a link between alterations in fimbria myelination and cognitive speed in mice.

Authors:  Takeshi Hiramoto; Akira Sumiyoshi; Takahira Yamauchi; Kenji Tanigaki; Qian Shi; Gina Kang; Rie Ryoke; Hiroi Nonaka; Shingo Enomoto; Takeshi Izumi; Manzoor A Bhat; Ryuta Kawashima; Noboru Hiroi
Journal:  Mol Psychiatry       Date:  2021-11-05       Impact factor: 13.437

3.  Advanced paternal age diversifies individual trajectories of vocalization patterns in neonatal mice.

Authors:  Lingling Mai; Hitoshi Inada; Ryuichi Kimura; Kouta Kanno; Takeru Matsuda; Ryosuke O Tachibana; Valter Tucci; Fumiyasu Komaki; Noboru Hiroi; Noriko Osumi
Journal:  iScience       Date:  2022-08-11
  3 in total

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