Genetic regulation of the placental transcriptome underlies birth weight and risk of childhood obesity.
Shouneng PengMaya A DeyssenrothAntonio F Di NarzoHaoxiang ChengZhongyang ZhangLuca LambertiniArno RuusaleppJason C KovacicJohan L M BjorkegrenCarmen J MarsitJia ChenKe HaoPublished in: PLoS genetics (2018)
GWAS identified variants associated with birth weight (BW), childhood obesity (CO) and childhood BMI (CBMI), and placenta is a critical organ for fetal development and postnatal health. We examined the role of placental transcriptome and eQTLs in mediating the genetic causes for BW, CO and CBMI, and applied integrative analysis (Colocalization and MetaXcan). GWAS loci associated with BW, CO, and CBMI were substantially enriched for placenta eQTLs (6.76, 4.83 and 2.26 folds, respectively). Importantly, compared to eQTLs of adult tissues, only placental eQTLs contribute significantly to both anthropometry outcomes at birth (BW) and childhood phenotypes (CO/CBMI). Eight, six and one transcripts colocalized with BW, CO and CBMI risk loci, respectively. Our study reveals that placental transcription in utero likely plays a key role in determining postnatal body size, and as such may hold new possibilities for therapeutic interventions to prevent childhood obesity.
Keyphrases
- birth weight
- genome wide
- gestational age
- weight gain
- copy number
- dna methylation
- gene expression
- genome wide association study
- body mass index
- preterm infants
- preterm birth
- healthcare
- rna seq
- public health
- single cell
- physical activity
- childhood cancer
- mental health
- transcription factor
- climate change
- early life
- metabolic syndrome
- social media
- insulin resistance
- young adults
- health promotion