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Data-Mining Approach on Transcriptomics and Methylomics Placental Analysis Highlights Genes in Fetal Growth Restriction

Authors :
Floris Chabrun
Noémie Huetz
Xavier Dieu
Guillaume Rousseau
Guillaume Bouzillé
Juan Manuel Chao de la Barca
Vincent Procaccio
Guy Lenaers
Odile Blanchet
Guillaume Legendre
Delphine Mirebeau-Prunier
Marc Cuggia
Philippe Guardiola
Pascal Reynier
Geraldine Gascoin
Source :
Frontiers in Genetics, Vol 10 (2020)
Publication Year :
2020
Publisher :
Frontiers Media S.A., 2020.

Abstract

Intrauterine Growth Restriction (IUGR) affects 8% of newborns and increases morbidity and mortality for the offspring even during later stages of life. Single omics studies have evidenced epigenetic, genetic, and metabolic alterations in IUGR, but pathogenic mechanisms as a whole are not being fully understood. An in-depth strategy combining methylomics and transcriptomics analyses was performed on 36 placenta samples in a case-control study. Data-mining algorithms were used to combine the analysis of more than 1,200 genes found to be significantly expressed and/or methylated. We used an automated text-mining approach, using the bulk textual gene annotations of the discriminant genes. Machine learning models were then used to explore the phenotypic subgroups (premature birth, birth weight, and head circumference) associated with IUGR. Gene annotation clustering highlighted the alteration of cell signaling and proliferation, cytoskeleton and cellular structures, oxidative stress, protein turnover, muscle development, energy, and lipid metabolism with insulin resistance. Machine learning models showed a high capacity for predicting the sub-phenotypes associated with IUGR, allowing a better description of the IUGR pathophysiology as well as key genes involved.

Details

Language :
English
ISSN :
16648021
Volume :
10
Database :
Directory of Open Access Journals
Journal :
Frontiers in Genetics
Publication Type :
Academic Journal
Accession number :
edsdoj.8863fff350a4dbc81549bb759719899
Document Type :
article
Full Text :
https://doi.org/10.3389/fgene.2019.01292