TARGETED ENRICHMENT STRATEGIES FOR NEXT-GENERATION PLANT BIOLOGY

被引:158
作者
Cronn, Richard [1 ]
Knaus, Brian J. [1 ]
Liston, Aaron [2 ]
Maughan, Peter J. [3 ]
Parks, Matthew [2 ]
Syring, John V. [4 ]
Udall, Joshua [3 ]
机构
[1] US Forest Serv, Pacific NW Res Stn, USDA, Corvallis, OR 97331 USA
[2] Oregon State Univ, Dept Bot & Plant Pathol, Corvallis, OR 97331 USA
[3] Brigham Young Univ, Dept Plant & Wildlife Sci, Provo, UT 84602 USA
[4] Linfield Coll, Dept Biol, Mcminneville, OR 97128 USA
基金
美国国家科学基金会;
关键词
target enrichment; genome reduction; hybridization; genotyping-by-sequencing; microfluidic PCR; multiplex PCR; transcriptome sequencing; SINGLE NUCLEOTIDE POLYMORPHISMS; DIFFERENTIAL EXPRESSION ANALYSIS; RNA-SEQ; SNP DISCOVERY; AMPLIFICATION PRODUCTS; GENOMIC REDUCTION; DIRECT SELECTION; DNA-SEQUENCES; PCR; TRANSCRIPTOME;
D O I
10.3732/ajb.1100356
中图分类号
Q94 [植物学];
学科分类号
071001 ;
摘要
Premise of the study: The dramatic advances offered by modern DNA sequencers continue to redefine the limits of what can be accomplished in comparative plant biology. Even with recent achievements, however, plant genomes present obstacles that can make it difficult to execute large-scale population and phylogenetic studies on next-generation sequencing platforms. Factors like large genome size, extensive variation in the proportion of organellar DNA in total DNA, polyploidy, and gene number/redundancy contribute to these challenges, and they demand flexible targeted enrichment strategies to achieve the desired goals. Methods: In this article, we summarize the many available targeted enrichment strategies that can be used to target partial-to-complete organellar genomes, as well as known and anonymous nuclear targets. These methods fall under four categories: PCR-based enrichment, hybridization-based enrichment, restriction enzyme-based enrichment, and enrichment of expressed gene sequences. Key results: Examples of plant-specific applications exist for nearly all methods described. While some methods are well established (e.g., transcriptome sequencing), other promising methods are in their infancy (hybridization enrichment). A direct comparison of methods shows that PCR-based enrichment may be a reasonable strategy for accessing small genomic targets (e.g., <= 50 kbp), but that hybridization and transcriptome sequencing scale more efficiently if larger targets are desired. Conclusions: While the benefits of targeted sequencing are greatest in plants with large genomes, nearly all comparative projects can benefit from the improved throughput offered by targeted multiplex DNA sequencing, particularly as the amount of data produced from a single instrument approaches a trillion bases per run.
引用
收藏
页码:291 / 311
页数:21
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