Department of Biomedical Sciences, Seoul National University College of Medicine, Seoul, Korea; Genomic Medicine Institute, Medical Research Center, Seoul National University, Seoul, Korea.
Department of Obstetrics and Gynecology, Seoul National University College of Medicine, Seoul, Korea.
HGG Adv. 2024 Apr 11;5(2):100276. doi: 10.1016/j.xhgg.2024.100276. Epub 2024 Feb 3.
Expression quantitative trait loci (eQTL) analysis measures the contribution of genetic variation in gene expression on complex traits. Although this methodology has been used to examine gene regulation in numerous human tissues, eQTL research in solid tissues is relatively lacking. We conducted eQTL analysis on placentas collected from an East Asian population in an effort to identify gene regulatory mechanisms in this tissue. Placentas (n = 102) were collected at the time of cesarean delivery. mRNA was extracted, sequenced with NGS, and compared with matched maternal and fetal DNA arrays performed using maternal and neonatal cord blood. Linear regression modeling was performed using tensorQTL. Fine-mapping along with epigenomic annotation was used to select putative functional variants. We identified 2,703 coding genes that contained at least one eQTL with statistical significance (false discovery rate <0.05). After fine-mapping, we found 108 previously unreported eQTL variants with posterior inclusion probability >0.1. Of these, 19% were located in genomic regions with evidence from public placental epigenome suggesting that they may be functionally relevant. For example, variant rs28379289 located in the placenta-specific regulatory region changes the binding affinity of transcription factor leading to higher expression of LGALS3, which is known to affect placental function. This study expands the knowledge base of regulatory elements within the human placenta and identifies 108 previously unreported placenta eQTL signals, which are listed in our publicly available GMI eQTL database. Further studies are needed to identify and characterize genetic regulatory mechanisms that affect placental function in normal pregnancy and placenta-related diseases.
表达数量性状基因座 (eQTL) 分析衡量基因变异对复杂性状基因表达的贡献。尽管这种方法已被用于研究许多人体组织中的基因调控,但在实体组织中进行 eQTL 研究相对较少。我们对来自东亚人群的胎盘进行了 eQTL 分析,以努力确定该组织中的基因调控机制。胎盘(n=102)是在剖宫产时收集的。提取 mRNA,用 NGS 进行测序,并与使用母血和新生儿脐带血进行的匹配母本和胎儿 DNA 阵列进行比较。使用 tensorQTL 进行线性回归建模。精细映射和表观基因组注释用于选择推定的功能变体。我们确定了 2703 个编码基因,其中至少有一个具有统计学意义的 eQTL(错误发现率<0.05)。精细映射后,我们发现了 108 个以前未报道的 eQTL 变体,其后验纳入概率>0.1。其中,19%位于具有公共胎盘表观基因组证据的基因组区域,表明它们可能具有功能相关性。例如,位于胎盘特异性调节区域的变体 rs28379289 改变了转录因子的结合亲和力,导致 LGALS3 的表达升高,已知其影响胎盘功能。这项研究扩展了人类胎盘内调节元件的知识库,并确定了 108 个以前未报道的胎盘 eQTL 信号,这些信号列在我们公开的 GMI eQTL 数据库中。需要进一步研究以确定和表征影响正常妊娠和胎盘相关疾病中胎盘功能的遗传调节机制。