德罗沙
生物
基因沉默
生物发生
生殖系
阿尔戈瑙特
计算生物学
掷骰子
小RNA
遗传学
人类遗传学
基因表达调控
RNA干扰
基因
核糖核酸
作者
Dylan Pelletier,Bárbara Rivera,Marc R. Fabian,William D. Foulkes
标识
DOI:10.1016/j.tig.2023.01.009
摘要
MicroRNAs (miRNAs) play vital roles in the regulation of gene expression, a process known as miRNA-induced gene silencing. The human genome codes for many miRNAs, and their biogenesis relies on a handful of genes, including DROSHA, DGCR8, DICER1, and AGO1/2. Germline pathogenic variants (GPVs) in these genes cause at least three distinct genetic syndromes, with clinical manifestations that range from hyperplastic/neoplastic entities to neurodevelopmental disorders (NDDs). Over the past decade, DICER1 GPVs have been shown to lead to tumor predisposition. Moreover, recent findings have provided insight into the clinical consequences arising from GPVs in DGCR8, AGO1, and AGO2. Here we provide a timely update with respect to how GPVs in miRNA biogenesis genes alter miRNA biology and ultimately lead to their clinical manifestations.
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