{"title":"Chd8 haploinsufficiency impacts rearing experience in C57BL/6 mice","authors":"Manal Tabbaa, Pat Levitt","doi":"10.1111/gbb.12892","DOIUrl":null,"url":null,"abstract":"<p>Mutations in <i>CHD8</i> are one of the highest genetic risk factors for autism spectrum disorder. Studies in mice that investigate underlying mechanisms have shown <i>Chd8</i> haploinsufficient mice display some trait disruptions that mimic clinical phenotypes, although inconsistencies have been reported in some traits across different models on the same strain background. One source of variation across studies may be the impact of <i>Chd8</i> haploinsufficiency on maternal-offspring interactions. While differences in maternal care as a function of <i>Chd8</i> genotype have not been studied directly, a previous study showed that pup survival was reduced when reared by <i>Chd8</i> heterozygous dams compared with wild-type (WT) dams, suggesting altered maternal care as a function of <i>Chd8</i> genotype. Through systematic observation of the C57BL/6 strain, we first determined the impact of <i>Chd8</i> haploinsufficiency in the offspring on WT maternal care frequencies across preweaning development. We next determined the impact of maternal <i>Chd8</i> haploinsufficiency on pup care. Compared with litters with all WT offspring, WT dams exhibited less frequent maternal behaviors toward litters consisting of offspring with mixed <i>Chd8</i> genotypes, particularly during postnatal week 1. Dam <i>Chd8</i> haploinsufficiency decreased litter survival and increased active maternal care also during postnatal week 1. Determining the impact of <i>Chd8</i> haploinsufficiency on early life experiences provides an important foundation for interpreting offspring outcomes and determining mechanisms that underlie heterogeneous phenotypes.</p>","PeriodicalId":50426,"journal":{"name":"Genes Brain and Behavior","volume":"23 2","pages":""},"PeriodicalIF":2.4000,"publicationDate":"2024-04-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://onlinelibrary.wiley.com/doi/epdf/10.1111/gbb.12892","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Genes Brain and Behavior","FirstCategoryId":"102","ListUrlMain":"https://onlinelibrary.wiley.com/doi/10.1111/gbb.12892","RegionNum":4,"RegionCategory":"心理学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"BEHAVIORAL SCIENCES","Score":null,"Total":0}
引用次数: 0
Abstract
Mutations in CHD8 are one of the highest genetic risk factors for autism spectrum disorder. Studies in mice that investigate underlying mechanisms have shown Chd8 haploinsufficient mice display some trait disruptions that mimic clinical phenotypes, although inconsistencies have been reported in some traits across different models on the same strain background. One source of variation across studies may be the impact of Chd8 haploinsufficiency on maternal-offspring interactions. While differences in maternal care as a function of Chd8 genotype have not been studied directly, a previous study showed that pup survival was reduced when reared by Chd8 heterozygous dams compared with wild-type (WT) dams, suggesting altered maternal care as a function of Chd8 genotype. Through systematic observation of the C57BL/6 strain, we first determined the impact of Chd8 haploinsufficiency in the offspring on WT maternal care frequencies across preweaning development. We next determined the impact of maternal Chd8 haploinsufficiency on pup care. Compared with litters with all WT offspring, WT dams exhibited less frequent maternal behaviors toward litters consisting of offspring with mixed Chd8 genotypes, particularly during postnatal week 1. Dam Chd8 haploinsufficiency decreased litter survival and increased active maternal care also during postnatal week 1. Determining the impact of Chd8 haploinsufficiency on early life experiences provides an important foundation for interpreting offspring outcomes and determining mechanisms that underlie heterogeneous phenotypes.
期刊介绍:
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