Maternal high-fat diet associated with altered gene expression, DNA methylation, and obesity risk in mouse offspring.
Madeline Rose KeleherRabab ZaidiShyam ShahM Elsa OakleyCassondra PavlatosSamir El IdrissiXiaoyun XingDaofeng LiTing WangJames M CheverudPublished in: PloS one (2018)
We investigated maternal obesity in inbred SM/J mice by assigning females to a high-fat diet or a low-fat diet at weaning, mating them to low-fat-fed males, cross-fostering the offspring to low-fat-fed SM/J nurses at birth, and weaning the offspring onto a high-fat or low-fat diet. A maternal high-fat diet exacerbated obesity in the high-fat-fed daughters, causing them to weigh more, have more fat, and have higher serum levels of leptin as adults, accompanied by dozens of gene expression changes and thousands of DNA methylation changes in their livers and hearts. Maternal diet particularly affected genes involved in RNA processing, immune response, and mitochondria. Between one-quarter and one-third of differentially expressed genes contained a differentially methylated region associated with maternal diet. An offspring high-fat diet reduced overall variation in DNA methylation, increased body weight and organ weights, increased long bone lengths and weights, decreased insulin sensitivity, and changed the expression of 3,908 genes in the liver. Although the offspring were more affected by their own diet, their maternal diet had epigenetic effects lasting through adulthood, and in the daughters these effects were accompanied by phenotypic changes relevant to obesity and diabetes.
Keyphrases
- high fat diet
- insulin resistance
- adipose tissue
- dna methylation
- weight loss
- gene expression
- high fat diet induced
- birth weight
- genome wide
- type diabetes
- pregnancy outcomes
- weight gain
- metabolic syndrome
- physical activity
- immune response
- body weight
- skeletal muscle
- glycemic control
- fatty acid
- cardiovascular disease
- pregnant women
- gestational age
- healthcare
- poor prognosis
- mental health
- dendritic cells
- copy number
- mechanical ventilation
- bioinformatics analysis
- bone mineral density
- soft tissue
- intensive care unit
- transcription factor
- mass spectrometry
- extracorporeal membrane oxygenation
- genome wide identification
- atomic force microscopy