Sorenson M D, Ast J C, Dimcheff D E, Yuri T, Mindell D P
Department of Biology, Boston University, Boston, Massachusetts 02215, USA.
Mol Phylogenet Evol. 1999 Jul;12(2):105-14. doi: 10.1006/mpev.1998.0602.
A PCR-based approach to sequencing complete mitochondrial genomes is described along with a set of 86 primers designed primarily for avian mitochondrial DNA (mtDNA). This PCR-based approach allows an accurate determination of complete mtDNA sequences that is faster than sequencing cloned mtDNA. The primers are spaced at about 500-base intervals along both DNA strands. Many of the primers incorporate degenerate positions to accommodate variation in mtDNA sequence among avian taxa and to reduce the potential for preferential amplification of nuclear pseudogenes. Comparison with published vertebrate mtDNA sequences suggests that many of the primers will have broad taxonomic utility. In addition, these primers should make available a wider variety of mitochondrial genes for studies based on smaller data sets.
本文描述了一种基于聚合酶链式反应(PCR)的方法来测序完整的线粒体基因组,并介绍了一组主要针对鸟类线粒体DNA(mtDNA)设计的86条引物。这种基于PCR的方法能够准确测定完整的mtDNA序列,且比克隆mtDNA测序更快。引物沿着两条DNA链以大约500个碱基的间隔排列。许多引物包含简并位点,以适应鸟类分类群中mtDNA序列的变异,并减少核假基因优先扩增的可能性。与已发表的脊椎动物mtDNA序列比较表明,许多引物具有广泛的分类学用途。此外,这些引物应为基于较小数据集的研究提供更多种类的线粒体基因。