Uemori Takashi, Mukai Hiroyuki, Takeda Osamu, Moriyama Mariko, Sato Yoshimi, Hokazono Shigekazu, Takatsu Nariaki, Asada Kiyozo, Kato Ikunoshin
Biotechnology Research Laboratories, Takara Bio Inc., Seta 3-4-1 Otsu, Shiga 520-2193, Japan.
J Biochem. 2007 Aug;142(2):283-92. doi: 10.1093/jb/mvm137. Epub 2007 Aug 24.
Isothermal and Chimeric primer-initiated Amplification of Nucleic acids (ICAN) allows the amplification of target DNA under isothermal conditions at around 55 degrees C using only a pair of 5'-DNA-RNA-3' chimeric primers, thermostable RNaseH and a DNA polymerase with strand-displacing activity (H. Mukai et al. J. Biochemistry, in the preceding paper in this issue). Here we elucidated the mechanism of ICAN by analysing the nicking site of RNaseH, behaviour of chimeric primers and extension products. We found that the ICAN reaction was composed of two unique mechanisms, multi-priming and template-switching, that were responsible for the highly efficient amplifying capability of ICAN. The simultaneous occurrence of two types of reactions, one based on multi-priming and the other based on template-switching, is likely to drive the DNA amplification in ICAN.
核酸等温嵌合引物引发扩增(ICAN)能够在约55摄氏度的等温条件下,仅使用一对5'-DNA-RNA-3'嵌合引物、耐热核糖核酸酶H和具有链置换活性的DNA聚合酶来扩增目标DNA(H. Mukai等人,《生物化学杂志》,本期上一篇论文)。在此,我们通过分析核糖核酸酶H的切口位点、嵌合引物的行为和延伸产物,阐明了ICAN的机制。我们发现ICAN反应由两种独特的机制组成,即多重引物引发和模板转换,这两种机制导致了ICAN的高效扩增能力。基于多重引物引发和基于模板转换的两种反应同时发生,可能推动了ICAN中的DNA扩增。