Identifying BMI-associated genes via a genome-wide multi-omics integrative approach using summary data

Author:

Tang Jingxian1,Xu Hanfei1,Xin Zihao1,Mei Quanshun1,Gao Musong1,Yang Tiantian1,Zhang Xiaoyu1,Levy Daniel234,Liu Ching-Ti1ORCID

Affiliation:

1. Department of Biostatistics, Boston University School of Public Health , 801 Massachusetts Ave, Boston, MA 02118 , United States

2. Framingham Heart Study, National Heart, Lung, and Blood Institute’s Framingham Heart Study , 73 Mt Wayte Ave, Framingham, MA , United States

3. Population Sciences Branch , National Heart, Lung, and Blood Institute, , 9000 Rockville Pike, Bethesda, MD , United States

4. National Institutes of Health , National Heart, Lung, and Blood Institute, , 9000 Rockville Pike, Bethesda, MD , United States

Abstract

Abstract Objective This study aims to identify BMI-associated genes by integrating aggregated summary information from different omics data. Methods We conducted a meta-analysis to leverage information from a genome-wide association study (n = 339 224), a transcriptome-wide association study (n = 5619), and an epigenome-wide association study (n = 3743). We prioritized the significant genes with a machine learning-based method, netWAS, which borrows information from adipose tissue-specific interaction networks. We also used the brain-specific network in netWAS to investigate genes potentially involved in brain-adipose interaction. Results We identified 195 genes that were significantly associated with BMI through meta-analysis. The netWAS analysis narrowed down the list to 21 genes in adipose tissue. Among these 21 genes, six genes, including FUS, STX4, CCNT2, FUBP1, NDUFS3, and RAPSN, were not reported to be BMI-associated in PubMed or GWAS Catalog. We also identified 11 genes that were significantly associated with BMI in both adipose and whole brain tissues. Conclusion This study integrated three types of omics data and identified a group of genes that have not previously been reported to be associated with BMI. This strategy could provide new insights for future studies to identify molecular mechanisms contributing to BMI regulation.

Funder

National Institute of Diabetes and Digestive and Kidney Diseases

National Heart, Lung, and Blood Institute

Publisher

Oxford University Press (OUP)

Subject

Genetics (clinical),Genetics,Molecular Biology,General Medicine

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