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Rapid SNP diagnostics using asymmetric isothermal amplification and a new mismatch-suppression technology
Authors:Mitani Yasumasa  Lezhava Alexander  Kawai Yuki  Kikuchi Takeshi  Oguchi-Katayama Atsuko  Kogo Yasushi  Itoh Masayoshi  Miyagi Toru  Takakura Hideki  Hoshi Kanako  Kato Chiaki  Arakawa Takahiro  Shibata Kazuhiro  Fukui Kenji  Masui Ryoji  Kuramitsu Seiki  Kiyotani Kazuma  Chalk Alistair  Tsunekawa Katsuhiko  Murakami Masami  Kamataki Tetsuya  Oka Takanori  Shimada Hiroshi  Cizdziel Paul E  Hayashizaki Yoshihide
Affiliation:Genome Exploration Research Group (Genome Network Project Core Group), RIKEN Genomic Sciences Center (GSC), RIKEN Yokohama Institute, 1-7-22 Suehiro-cho, Tsurumi-ku, Yokohama, Kanagawa, 230-0045, Japan.
Abstract:
We developed a rapid single nucleotide polymorphism (SNP) detection system named smart amplification process version 2 (SMAP 2). Because DNA amplification only occurred with a perfect primer match, amplification alone was sufficient to identify the target allele. To achieve the requisite fidelity to support this claim, we used two new and complementary approaches to suppress exponential background DNA amplification that resulted from mispriming events. SMAP 2 is isothermal and achieved SNP detection from whole human blood in 30 min when performed with a new DNA polymerase that was cloned and isolated from Alicyclobacillus acidocaldarius (Aac pol). Furthermore, to assist the scientific community in configuring SMAP 2 assays, we developed software specific for SMAP 2 primer design. With these new tools, a high-precision and rapid DNA amplification technology becomes available to aid in pharmacogenomic research and molecular-diagnostics applications.
Keywords:
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