Abstract

BackgroundChloroplast genomes supply valuable genetic information for evolutionary and functional studies in plants. The past five years have witnessed a dramatic increase in the number of completely sequenced chloroplast genomes with the application of second-generation sequencing technology in plastid genome sequencing projects. However, cost-effective high-throughput chloroplast DNA (cpDNA) extraction becomes a major bottleneck restricting the application, as conventional methods are difficult to make a balance between the quality and yield of cpDNAs.Methodology/Principal FindingsWe first tested two traditional methods to isolate cpDNA from the three species, Oryza brachyantha, Leersia japonica and Prinsepia utihis. Both of them failed to obtain properly defined cpDNA bands. However, we developed a simple but efficient method based on sucrose gradients and found that the modified protocol worked efficiently to isolate the cpDNA from the same three plant species. We sequenced the isolated DNA samples with Illumina (Solexa) sequencing technology to test cpDNA purity according to aligning sequence reads to the reference chloroplast genomes, showing that the reference genome was properly covered. We show that 40–50% cpDNA purity is achieved with our method.ConclusionHere we provide an improved method used to isolate cpDNA from angiosperms. The Illumina sequencing results suggest that the isolated cpDNA has reached enough yield and sufficient purity to perform subsequent genome assembly. The cpDNA isolation protocol thus will be widely applicable to the plant chloroplast genome sequencing projects.

Highlights

  • Chloroplasts are plant organelles that contain a circular DNA containing,130 genes with the size ranging from 72 to 217 kb [1,2]. chloroplast DNA (cpDNA) of green plants are exceptionally conserved in their gene content and organization, providing sufficient information for genome-wide evolutionary studies

  • The cpDNA isolation protocol will be widely applicable to the plant chloroplast genome sequencing projects

  • The former method is polymerase chain reaction (PCR)-based cpDNA sequencing, which is usually used to the situation that substantial plant leaf materials (e.g.,20 to 100 g fresh leaves) are unavailable but can be substituted by extracting total DNA from limited materials

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Summary

Conclusion

We provide an improved method used to isolate cpDNA from angiosperms. The Illumina sequencing results suggest that the isolated cpDNA has reached enough yield and sufficient purity to perform subsequent genome assembly. The cpDNA isolation protocol will be widely applicable to the plant chloroplast genome sequencing projects

Introduction
Results and Discussion
Materials and Methods

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