Morse Daniel P
Chemistry Department, United States Naval Academy, Annapolis, MD, USA.
Methods Mol Biol. 2004;265:199-218. doi: 10.1385/1-59259-775-0:199.
Adenosine deaminases that acts on RNA (ADARs) are RNA-editing enzymes that convert adenosine to inosine in double-stranded RNA. This chapter provides a detailed protocol for identifying inosine-containing RNAs. Candidate ADAR substrates are identified by cleaving poly (A)+ RNA specifically after inosine and using differential display to detect cleaved molecules. To confirm the presence of inosine, each individual candidate substrate is amplified by reverse transcriptase polymerase chain reaction (RT-PCR) and the PCR product is directly sequenced. Sites that contain inosine at the RNA level appear as a mixture of adenosine and guanosine in the cDNA. The relative peak areas provide an estimate of the extent of editing at each site.
作用于RNA的腺苷脱氨酶(ADARs)是一类RNA编辑酶,可将双链RNA中的腺苷转化为次黄苷。本章提供了一份详细的鉴定含次黄苷RNA的实验方案。通过在次黄苷后特异性切割聚腺苷酸(poly(A)+)RNA,并利用差异显示来检测切割后的分子,从而鉴定出ADAR候选底物。为确认次黄苷的存在,通过逆转录聚合酶链反应(RT-PCR)扩增每个单独的候选底物,并对PCR产物进行直接测序。在RNA水平含有次黄苷的位点在cDNA中表现为腺苷和鸟苷的混合物。相对峰面积可估计每个位点的编辑程度。