Genesis Research and Development Corporation Limited, Auckland, New Zealand.
Nucleic Acids Res. 2010 Jan;38(3):e19. doi: 10.1093/nar/gkp1076. Epub 2009 Nov 26.
Specific detection of mRNA cleavage by 5'RACE is the only method to confirm the knockdown of mRNA by RNA interference, but is rarely reported for in vivo studies. We have combined 5'-RNA-linker-mediated RACE (5'-RLM-RACE) with real-time PCR using a molecular beacon to develop a rapid and specific method termed MBRACE, which we have used to detect small-interfering RNA (siRNA)-induced cleavage of ApoB, RRM1 and YBX1 transcripts in vitro, and ApoB in vivo. When RNA from siRNA-transfected cells was used for 5'-RLM-RACE and a cleavage site-specific molecular beacon probe was included in subsequent real-time PCR analysis, the specific mRNA cleavage product was detected. Detection of siRNA-mediated cleavage was also observed when RNA from mouse liver following administration of ApoB-specific siRNA was analysed, even in cases where ApoB knockdown measured by real-time PCR was <10%. With its sensitivity and specificity, this variation on the 5'RACE method should prove a useful tool to detect mRNA cleavage and corroborate knockdown studies following siRNA use in vivo.
通过 5'RACE 进行特定的 mRNA 切割检测是唯一能够确认 RNA 干扰导致 mRNA 敲低的方法,但很少有用于体内研究的报道。我们已经将 5'-RNA 接头介导的 RACE(5'-RLM-RACE)与使用分子信标进行的实时 PCR 相结合,开发了一种称为 MBRACE 的快速而特异的方法,我们已经使用该方法检测了体外小干扰 RNA(siRNA)诱导的 ApoB、RRM1 和 YBX1 转录本以及体内 ApoB 的切割。当使用转染了 siRNA 的细胞的 RNA 进行 5'-RLM-RACE 时,并在随后的实时 PCR 分析中包含了切割位点特异性的分子信标探针,就可以检测到特定的 mRNA 切割产物。当分析给予 ApoB 特异性 siRNA 后小鼠肝脏中的 RNA 时,也观察到了 siRNA 介导的切割,即使实时 PCR 测量的 ApoB 敲低<10%。这种 5'RACE 方法的变体具有敏感性和特异性,应该是一种有用的工具,可用于检测体内使用 siRNA 后 mRNA 的切割,并证实敲低研究。