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• W3048578375 abstract "Abstract Background Previous expression quantitative trait loci (eQTL) studies have identified thousands of genetic variants to be associated with gene expression at the mRNA level in the human liver. However, protein expression often correlates poorly with mRNA levels. Thus, protein quantitative trait loci (pQTL) study is required to identify genetic variants that regulate protein expression in human livers. Results We conducted a genome-wide pQTL study in 287 normal human liver samples and identified 900 local pQTL variants and 4026 distant pQTL variants. We further discovered 53 genome hotspots of pQTL variants. Transcriptional region mapping analysis showed that 1133 pQTL variants are in transcriptional regulatory regions. Genomic region enrichment analysis of the identified pQTL variants revealed 804 potential regulatory interactions among 595 predicted regulators (e.g., non-coding RNAs) and 394 proteins. Moreover, pQTL variants and trait-variant integration analysis implied several novel mechanisms underlying the relationships between protein expression and liver diseases, such as alcohol dependence. Notably, over 2000 of the identified pQTL variants have not been reported in previous eQTL studies, suggesting extensive involvement of genetic polymorphisms in post-transcriptional regulation of protein expression in human livers. Conclusions We have partially established protein expression regulation networks in human livers and generated a wealth of pQTL data that could serve as a valuable resource for the scientific community." @default.
• W3048578375 created "2020-08-18" @default.
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• W3048578375 date "2020-08-10" @default.
• W3048578375 modified "2023-10-13" @default.
• W3048578375 title "Genome-wide pQTL analysis of protein expression regulatory networks in the human liver" @default.
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• W3048578375 doi "https://doi.org/10.1186/s12915-020-00830-3" @default.
• W3048578375 hasPubMedCentralId "https://www.ncbi.nlm.nih.gov/pmc/articles/7418398" @default.
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• W3048578375 hasPublicationYear "2020" @default.
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