生物
RNA连接酶
互补DNA
信使核糖核酸
寡核苷酸
分子生物学
核糖核酸
逆转录酶
cDNA末端的快速扩增
焦磷酸酶
生物化学
酶
DNA
基因
分子克隆
作者
Kazuo Maruyama,Sumio Sugano
出处
期刊:Gene
[Elsevier BV]
日期:1994-01-01
卷期号:138 (1-2): 171-174
被引量:584
标识
DOI:10.1016/0378-1119(94)90802-8
摘要
We have devised a method to replace the cap structure of a mRNA with an oligoribonucleotide (r-oligo) to label the 5′ end of eukaryotic mRNAs. The method consists of removing the cap with tobacco acid pyrophosphatase (TAP) and ligating r-oligos to decapped mRNAs with T4 RNA ligase. This reaction was made cap-specific by removing 5′-phosphates of non-capped RNAs with alkaline phosphatase prior to TAP treatment. Unlike the conventional methods that label the 5′ end of cDNAs, this method specifically labels the capped end of the mRNAs with a synthetic r-oligo prior to first-strand cDNA synthesis. The 5′ end of the mRNA was identified quite simply by reverse transcription-polymerase chain reaction (RT-PCR).
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