生物
小RNA
核糖核酸
cDNA文库
小RNA
基因
分子生物学
互补DNA
cDNA末端的快速扩增
计算生物学
遗传学
分子克隆
作者
Hanjiang Fu,Yi Tie,Chengwang Xu,Zhuoyuan Zhang,Jie Zhu,Yingxu Shi,Hong Jiang,Zhixian Sun,Xiaofei Zheng
出处
期刊:FEBS Letters
[Wiley]
日期:2005-06-14
卷期号:579 (17): 3849-3854
被引量:199
标识
DOI:10.1016/j.febslet.2005.05.064
摘要
MicroRNAs (miRNAs) are short 20-25 nucleotides RNA molecules that have been shown to regulate gene expressions in a variety of eukaryotic systems. miRNAs are widespread in eukaryotes and several hundred of miRNAs have been identified, but still a lot of miRNAs have not been detected in various eukaryotic organisms. However, it is not an easy work to clone miRNAs by traditional methods. Here, we describe the identification of 27 miRNAs from a human fetal liver cDNA library by a novel cloning method. Low molecular weight RNA fraction (< or = 200 nt) from fetal liver tissue was extracted, and polyadenylated by poly(A) polymerase. A 5' RNA adaptor was ligated to poly(A)-tailed RNA using T4 RNA ligase. After reverse transcription, the cDNA was amplified by PCR with two adaptor primers. The PCR product with a size about 109 bp was recovered and cloned into T vector. After sequencing, database searching, and expression profiling, 5 novel miRNAs were discovered among other 22 known miRNAs in human fetal liver. These finding indicate that a large diverse population of miRNAs may function to regulate gene expression in hepatocyte.
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