Impact of fetal expression quantitative trait loci on transcriptome-wide association study of childhood leukemia

Author:

Yang Tianzhong12ORCID,Mills Lauren J23,Xue Haoran4,Raduski Andrew3,Williams Lindsay A235,Spector Logan G23

Affiliation:

1. Department of Biostatistics, School of Public Health, University of Minnesota, MN, USA

2. Masonic Cancer Center, University of Minnesota, Minneapolis, MN, USA

3. Division of Epidemiology and Clinical Research, Department of Pediatrics, University of Minnesota School of Medicine, Minneapolis, MN, USA

4. Department of Statistics, University of Minnesota, MN, USA

5. Brain Tumor Program, University of Minnesota, Minneapolis, MN, USA

Abstract

Abstract Transcriptome-wide association studies increase the yield of loci associated with disease phenotypes by focusing on expression quantitative trait loci (eQTL). The major source of eQTL data for is the Gene and Tissue Expression (GTEx) project, which is comprised entirely of adults, mainly those >50 years of age at death. Since gene expression levels differ by developmental stage, it is not clear whether eQTLs derived from adult data sources are best suited for use in young-onset diseases such as pediatric cancers. To fill in this knowledge gap, we performed a large-scale eQTL mapping analysis in the GenCord study with newborn samples and compared it with GTEx. Under matched conditions, we found around 80% of the eQTLs in one study can be replicated in the other. However, among all eQTLs identified in GenCord (GTEx), 584 (1045) showed statistically significant differences in effect sizes in GTEx (GenCord). We further investigated how using fetal eQTL data can facilitate the genetic association study of acute lymphoblastic leukemia. GenCord and GTEx identified the same genetic loci with statistical significance; however, the overall association pattern was only weakly correlated. Our paper demonstrates age-differential eQTLs and shows their potential influence on childhood leukemia research.

Funder

Children's Cancer Research Fund

Publisher

Oxford University Press (OUP)

Subject

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

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