5' RNase activity of Phi29 DNA polymerase converts target RNA into a primer and the polyme'/> Novel application of Phi29 DNA polymerase: RNA detection and analysis in vitro and in situ by target RNA-primed RCA.
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Novel application of Phi29 DNA polymerase: RNA detection and analysis in vitro and in situ by target RNA-primed RCA.

机译:Phi29 DNA聚合酶的新应用:目标RNA引发的RCA在体外和原位进行RNA检测和分析。

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摘要

We present a novel Phi29 DNA polymerase application in RCA-based target RNA detection and analysis. The 3'-->5' RNase activity of Phi29 DNA polymerase converts target RNA into a primer and the polymerase uses this newly generated primer for RCA initiation. Therefore, using target RNA-primed RCA, padlock probes may be targeted to inner RNA sequences and their peculiarities can be analyzed directly. We demonstrate that the exoribonucleolytic activity of Phi29 DNA polymerase can be successfully applied in vitro and in situ. These findings expand the potential for detection and analysis of RNA sequences distanced from 3'-end.
机译:我们提出了一种新型的Phi29 DNA聚合酶在基于RCA的靶RNA检测和分析中的应用。 Phi29 DNA聚合酶的3'-> 5'RNase活性将靶RNA转化为引物,聚合酶使用这种新生成的引物进行RCA起始。因此,使用目标RNA引发的RCA,挂锁探针可以靶向内部RNA序列,并且可以直接分析其特殊性。我们证明Phi29 DNA聚合酶的exoribonucleolytic活性可以成功地在体外和原位应用。这些发现扩大了检测和分析距3'-末端的RNA序列的潜力。

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