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A primer-based approach to genome walking

机译:基于引物的基因组行走方法

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摘要

A genome walking strategy based on annealing and ligation of single-stranded DNA primers to 3′ overhangs following restriction endonuclease digestion was developed. A set of primers contains 4 nucleotides at the 3′ end that are complementary to overhangs formed by restriction endonucleasesApaI;PstI;SacI andSphI. Following ligation, 5′ end overhangs are formed on the DNA, which serves as sites for the adaptor primers and nested primers for PCR amplification in combination with the gene-specific primers. This strategy was verified by the amplification of up to 4 kb of a potato leafroll virus full-length infectious clone. The procedure could be adopted to target any upstream and downstream regions flanking known sequences within the plant genome.
机译:开发了基于限制性内切核酸酶消化后单链DNA引物退火和连接至3'突出端的基因组步移策略。一组引物在3'端含有4个核苷酸,它们与限制性核酸内切酶ApaI; PstI; SacI和SphI形成的突出端互补。连接后,在DNA上形成5'末端突出端,与基因特异性引物结合在一起,用作PCR扩增的衔接子引物和嵌套引物的位点。通过扩增多达4 kb的马铃薯卷叶病毒全长感染性克隆,验证了该策略。可以采用该方法靶向植物基因组内已知序列侧翼的任何上游和下游区域。

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