The Goldyne Savad Institute for Gene Therapy, Hadassah Hebrew University Hospital, Jerusalem, Israel.
PLoS One. 2009 Oct 20;4(10):e7511. doi: 10.1371/journal.pone.0007511.
microRNAs (miRNAs) are small noncoding RNAs that regulate cognate mRNAs post-transcriptionally. miRNAs have been implicated in regulating gene expression in embryonic developmental processes, including proliferation and differentiation. The liver is a multifunctional organ, which undergoes rapid changes during the developmental period and relies on tightly-regulated gene expression. Little is known regarding the complex expression patterns of both mRNAs and miRNAs during the early stages of human liver development, and the role of miRNAs in the regulation of this process has not been studied. The aim of this work was to study the impact of miRNAs on gene expression during early human liver development.
Global gene and miRNA expression were profiled in adult and in 9-12w human embryonic livers, using high-density microarrays and quantitative RT-PCR.
Embryonic liver samples exhibited a gene expression profile that differentiated upon progression in the developmental process, and revealed multiple regulated genes. miRNA expression profiling revealed four major expression patterns that correlated with the known function of regulated miRNAs. Comparison of the expression of the most regulated miRNAs to that of their putative targets using a novel algorithm revealed a significant anti-correlation for several miRNAs, and identified the most active miRNAs in embryonic and in adult liver. Furthermore, our algorithm facilitated the identification of TGFbeta-R1 as a novel target gene of let-7.
Our results uncover multiple regulated miRNAs and genes throughout human liver development, and our algorithm assists in identification of novel miRNA targets with potential roles in liver development.
microRNAs(miRNAs)是一种小的非编码 RNA,可以在转录后调节同源 mRNA 的表达。miRNAs 参与调节胚胎发育过程中的基因表达,包括增殖和分化。肝脏是一个多功能器官,在发育过程中会发生快速变化,并且依赖于严格调控的基因表达。关于人类肝脏早期发育过程中 mRNA 和 miRNAs 的复杂表达模式知之甚少,并且 miRNAs 在调节这一过程中的作用尚未得到研究。本研究旨在研究 miRNAs 在早期人类肝脏发育过程中对基因表达的影响。
使用高密度微阵列和定量 RT-PCR 对成人和 9-12w 人类胚胎肝脏进行了全局基因和 miRNA 表达谱分析。
胚胎肝脏样本表现出随发育过程进展而分化的基因表达谱,并揭示了多个受调控的基因。miRNA 表达谱分析揭示了与调节 miRNA 已知功能相关的四种主要表达模式。使用新算法比较最受调节的 miRNA 与其假定靶基因的表达显示,几种 miRNA 呈显著负相关,并鉴定了胚胎和成人肝脏中最活跃的 miRNA。此外,我们的算法有助于鉴定 TGFbeta-R1 为 let-7 的新靶基因。
我们的研究结果揭示了人类肝脏发育过程中多个受调节的 miRNAs 和基因,并且我们的算法有助于鉴定在肝脏发育中具有潜在作用的新 miRNA 靶基因。