Comparative transcriptomic and metabolomic analysis of FTO knockout and wild-type porcine iliac artery endothelial cells
- Libao Xie 1, Ninglin Fan 2, Xiaoting Ding 2, Taohua Zhang 3, Wei Wang 2, Pengyuan Ji 2, Huijuan Wu 2
- Libao Xie 1, Ninglin Fan 2, Xiaoting Ding 2
- 1Beijing Laboratory Animal Research Center, Co., Ltd., Beijing 102609, China; Beijing Academy of Science and Technology, Beijing 100089, China.
- 2Beijing Laboratory Animal Research Center, Co., Ltd., Beijing 102609, China.
- 3The Seventh Department of General Surgery, The First Hospital of Lanzhou University, Lanzhou 730000, Gansu, China.
- 0Beijing Laboratory Animal Research Center, Co., Ltd., Beijing 102609, China; Beijing Academy of Science and Technology, Beijing 100089, China.
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View abstract on PubMed
Summary
This summary is machine-generated.The fat mass and obesity associated (FTO) gene knockout reveals significant changes in cell gene expression and metabolism. This study uncovers FTO
Area Of Science
- Molecular Biology
- Genetics
- Metabolomics
Background
- The fat mass and obesity associated (FTO) gene is a key genetic factor in adiposity.
- Emerging evidence links the FTO gene to various cancer types.
- Understanding FTO's cellular functions is crucial for its role in disease.
Purpose Of The Study
- To investigate the FTO gene's function and impact on cellular processes.
- To analyze gene expression and metabolic changes in FTO-deficient cells.
- To explore the molecular mechanisms underlying FTO's role in health and disease.
Main Methods
- Established an FTO knockout (KO) cell line in porcine iliac artery endothelial cells (PIECs) using CRISPR/Cas9 technology.
- Conducted comprehensive transcriptomic and metabolomic analyses to compare FTO KO and wild-type (WT) cells.
- Performed enrichment analysis and correlation studies between gene expression and metabolite profiles.
Main Results
- Significant differences in gene expression and metabolic profiles were observed between FTO KO and WT cells.
- Enrichment analysis identified involvement in metabolic pathways, cellular functions, and disease-related cascades (e.g., atherosclerosis, insulin signaling).
- Metabolomic profiling showed distinct metabolic alterations in FTO KO cells, with melatonin correlating with multiple gene expressions.
Conclusions
- FTO gene deficiency profoundly impacts cellular gene expression and metabolism.
- The study highlights FTO's involvement in diverse biological pathways, including metabolic and signaling processes.
- Findings provide a basis for further research into FTO's role in physiological and pathological conditions.
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