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长度多态性扫描是揭示叶绿体DNA变异的一种有效方法。

Length polymorphism scanning is an efficient approach for revealing chloroplast DNA variation.

作者信息

Horning Matthew E, Cronn Richard C

机构信息

USDA Forest Service, Pacific Northwest Research Station, Corvallis, OR 97331, USA.

出版信息

Genome. 2006 Feb;49(2):134-42. doi: 10.1139/g05-093.

DOI:10.1139/g05-093
PMID:16498463
Abstract

Phylogeographic and population genetic screens of chloroplast DNA (cpDNA) provide insights into seed-based gene flow in angiosperms, yet studies are frequently hampered by the low mutation rate of this genome. Detection methods for intraspecific variation can be either direct (DNA sequencing) or indirect (PCR-RFLP), although no single method incorporates the best features of both approaches. We show that screening universal chloroplast amp li cons for length polymorphism provides an accurate and efficient method for identifying cpDNA variation. By sequencing 4500 bp of cpDNA from 17 accessions of Purshia tridentata (bitterbrush), we detected 9 haplotypes, 8 of which were identifiable by unique multilocus length combinations resolvable by automated fragment analysis. In silico estimates of PCR-RFLP for these loci show that 5 haplotypes would be resolved by agarose electrophoresis. A survey of 4 intraspecific data sets from diverse angiosperms revealed that length variation in cpDNA amplicons is nearly ubiquitous, and 61 of 67 haplotypes identified by direct sequencing could be identified by screening length variation. Combined with automated fluorescent detection, length polymorphism screening of universal cpDNA regions offers a simple screen for intraspecific variation that can be used across angiosperms with minimal optimization, providing detection limits that rival direct sequencing at a fraction of the cost.

摘要

叶绿体DNA(cpDNA)的系统地理学和群体遗传学筛选为被子植物基于种子的基因流提供了见解,但该基因组的低突变率常常阻碍相关研究。种内变异的检测方法可以是直接的(DNA测序)或间接的(PCR-RFLP),不过没有一种单一方法能兼具这两种方法的最佳特性。我们表明,筛选通用叶绿体扩增子的长度多态性为鉴定cpDNA变异提供了一种准确且高效的方法。通过对17个三齿苦木(bitterbrush)样本的4500 bp cpDNA进行测序,我们检测到9种单倍型,其中8种可通过自动片段分析解析的独特多位点长度组合来识别。对这些位点的PCR-RFLP进行的电子估计表明,5种单倍型可通过琼脂糖电泳解析。对来自不同被子植物的4个种内数据集的调查显示,cpDNA扩增子的长度变异几乎普遍存在,通过直接测序鉴定的67种单倍型中的61种可通过筛选长度变异来识别。结合自动荧光检测,通用cpDNA区域的长度多态性筛选为种内变异提供了一种简单的筛选方法,该方法可在几乎无需优化的情况下用于整个被子植物,提供的检测限可与直接测序相媲美,而成本仅为其一小部分。

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