Yamauchi Mitsugu M, Miya Masaki U, Machida Ryuji J, Nishida Mutsumi
Ocean Research Institute, University of Tokyo, 1-15-1 Minamidai, Nakano-ku, Tokyo 164-8639, Japan.
Mar Biotechnol (NY). 2004 Sep-Oct;6(5):419-29. doi: 10.1007/s10126-003-0036-2. Epub 2004 May 13.
An approach for sequencing the entire mitochondrial genomes (mitogenomes) of decapod crustaceans using 79 newly designed and 7 published polymerase chain reaction (PCR) primers is described. The approach comprises the following steps: (1) the entire mitogenome is amplified in 2 or 3 long PCRs; (2) the 86 primers are used in different combinations to amplify contiguous, overlapping short segments of the entire mitogenome with the diluted long PCR products as templates; (3) direct cycle sequencing is conducted using the short PCR products. This strategy allows a more rapid determination of decapod mitogenomic sequences than a traditional method using cloned mitochondrial DNA and primer walking strategy. As a practical example, the mitogenomic sequence for a kuruma prawn Marsupenaeus japonicus (Crustacea: Decapoda), was determined using the PCR-based approach.
本文描述了一种使用79种新设计的和7种已发表的聚合酶链反应(PCR)引物对十足目甲壳类动物的整个线粒体基因组(线粒体基因组)进行测序的方法。该方法包括以下步骤:(1)通过2次或3次长PCR扩增整个线粒体基因组;(2)以稀释后的长PCR产物为模板,将86种引物以不同组合用于扩增整个线粒体基因组的连续、重叠短片段;(3)使用短PCR产物进行直接循环测序。与使用克隆线粒体DNA和引物步移策略的传统方法相比,该策略能够更快地确定十足目线粒体基因组序列。作为一个实际例子,使用基于PCR的方法确定了日本对虾(甲壳纲:十足目)的线粒体基因组序列。