Genetic architecture of microRNA expression and its link to complex diseases in the Japanese population

• Published in: Human molecular genetics 2022-06, Vol.31 (11), p.1806-1820
• Main Authors: Sonehara, Kyuto, Sakaue, Saori, Maeda, Yuichi, Hirata, Jun, Kishikawa, Toshihiro, Yamamoto, Kenichi, Matsuoka, Hidetoshi, Yoshimura, Maiko, Nii, Takuro, Ohshima, Shiro, Kumanogoh, Atsushi, Okada, Yukinori
• Format: Article
• Language: English
• Subjects: Adult; Diabetes Mellitus, Type 2; DNA Copy Number Variations; Genome-Wide Association Study; Humans; Japan; MicroRNAs - genetics; MicroRNAs - metabolism; Original; Polymorphism, Single Nucleotide - genetics; RNA, Untranslated
• ISSN: 0964-6906; 1460-2083
• DOI: 10.1093/hmg/ddab361

Understanding the genetic effects on non-coding RNA (ncRNA) expression facilitates functional characterization of disease-associated genetic loci. Among several classes of ncRNAs, microRNAs (miRNAs) are key post-transcriptional gene regulators. Despite its biological importance, previous studies on the genetic architecture of miRNA expression focused mostly on the European individuals, underrepresented in other populations. Here, we mapped miRNA expression quantitative trait loci (miRNA-eQTL) for 343 miRNAs in 141 Japanese using small RNA sequencing and whole-genome sequencing, identifying 1275 cis-miRNA-eQTL variants for 40 miRNAs (false discovery rate < 0.2). Of these, 25 miRNAs having eQTL were unreported in the European studies, including 5 miRNAs with their lead variant monomorphic in the European populations, which demonstrates the value of miRNA-eQTL analysis in diverse ancestral populations. MiRNAs with eQTL effect showed allele-specific expression (ASE; e.g. miR-146a-3p), and ASE analysis further detected cis-regulatory variants not captured by the conventional miRNA-eQTL mapping (e.g. miR-933). We identified a copy number variation associated with miRNA expression (e.g. miR-570-3p, P = 7.2 × 10-6), which contributes to a more comprehensive landscape of miRNA-eQTLs. To elucidate a post-transcriptional modification in miRNAs, we created a catalog of miRNA-editing sites, including 10 canonical and 6 non-canonical sites. Finally, by integrating the miRNA-eQTLs and Japanese genome-wide association studies of 25 complex traits (mean n = 192 833), we conducted a transcriptome-wide association study, identifying miR-1908-5p as a potential mediator for adult height, colorectal cancer and type 2 diabetes (P < 9.1 × 10-5). Our study broadens the population diversity in ncRNA-eQTL studies and contributes to functional annotation of disease-associated loci found in non-European populations.