Expression Changes in Epigenetic Gene Pathways Associated With One-Carbon Nutritional Metabolites in Maternal Blood

Yihui Zhu1,2, Charles E Mordaunt1,2, Blythe P Durbin-Johnson3

  • 1Department of Medical Microbiology and Immunology, Genome Center, and Perinatal Origins of Disparities Center, University of California, Davis, California, USA.

Insights

Maternal nutrient metabolites during pregnancy are linked to gene expression changes in mothers of children later diagnosed with autism spectrum disorder (ASD). These findings highlight the role of prenatal nutrition in neurodevelopmental outcomes.

Area of Science:

  • Neuroscience
  • Genetics
  • Nutritional Science

Background:

  • The prenatal period is critical for neurodevelopment and autism spectrum disorder (ASD) risk.
  • The interplay between maternal nutrition, specifically one-carbon metabolites, and gestational gene expression in relation to ASD is not well understood.

Purpose of the Study:

  • To investigate the association between prenatal one-carbon metabolites and maternal blood gene expression in mothers of children later diagnosed with ASD or non-typical development (Non-TD).
  • To identify specific gene pathways and transcripts affected by nutrient status during pregnancy relevant to neurodevelopmental outcomes.

Main Methods:

  • Genome-wide transcriptomes were analyzed from 300 maternal blood samples using microarrays.
  • Levels of sixteen one-carbon metabolites, including folic acid, betaine, 5-methyltetrahydrofolate (5-MeTHF), and dimethylglycine (DMG), were measured.
  • Differential gene expression analysis and weighted gene correlation network analysis (WGCNA) were employed to correlate gene expression with child neurodevelopmental outcomes and metabolite levels.

Main Results:

  • Six transcripts (TGR-AS1, SQSTM1, HLA-C, and RFESD) were significantly associated with child outcomes (ASD, Non-TD, TD).
  • WGCNA revealed gene modules significantly correlated with folic acid, 5-MeTHF, DMG, and betaine.
  • A DNA methylation-enriched module showed a protective association with folic acid/5-MeTHF and ASD risk; maternal betaine and DMG were linked to genes involved in immune function and gene regulation.

Conclusions:

  • Prenatal maternal blood transcriptome reflects gestational one-carbon metabolite status and is associated with neurodevelopmental outcomes.
  • Maternal nutrient status during pregnancy influences gene expression pathways relevant to ASD risk and neurodevelopment.

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