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Updated: Mar 25, 2026

Transcriptional Analysis by Nascent RNA FISH of In Vivo Trophoblast Giant Cells or In Vitro Short-term Cultures of Ectoplacental Cone Explants
Published on: August 31, 2016
Gestational diabetic transcriptomic profiling of microdissected human trophoblast
Muhammad Furqan Bari1, Sherry Ngo2, Claire C Bastie3
1Department of PathologyDow International Medical College, Karachi, Pakistan.
Gestational diabetes mellitus (GDM) is linked to specific placental gene expression changes, particularly in RNA processing and ubiquitination, even when accounting for obesity. These findings help clarify GDM
Area of Science:
- Obstetrics and Gynecology
- Metabolic Disorders
- Genomics
Background:
- Gestational diabetes mellitus (GDM) is a common pregnancy complication.
- Obesity is a significant risk factor for GDM.
- Placental heterogeneity complicates GDM research.
Purpose of the Study:
- To identify genes differentiating GDM from obesity in placental trophoblast.
- To investigate the role of RNA processing and ubiquitination in GDM.
- To understand the relationship between gene expression and maternal glucose levels in GDM.
Main Methods:
- Laser capture microdissection (LCM) for placental trophoblast isolation.
- Genome-wide gene expression analysis (transcriptomic profiling).
- Statistical analysis to identify differentially expressed genes (DEGs).
Main Results:
- Forty-five DEGs distinguished GDM from matched obese placentae.
- Increased PSG6 and SLC38A1 expression in GDM.
- DEGs involved in RNA processing, splicing, and ubiquitination correlated with maternal fasting plasma glucose.
Conclusions:
- Specific DEGs discriminate GDM from obesity.
- A biological link exists between RNA processing/ubiquitination genes and GDM pathophysiology.
- These findings provide insights into GDM etiology, controlling for obesity.
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