Hewitt Seanna, Kilian Benjamin, Hari Ramyya, Koepke Tyson, Sharpe Richard, Dhingra Amit
Molecular Plant Sciences Graduate Program, Washington State University, Pullman, WA 99164, United States; Department of Horticulture, Washington State University, Pullman, WA 99164-6414, United States.
Department of Horticulture, Washington State University, Pullman, WA 99164-6414, United States.
Comput Struct Biotechnol J. 2017 Mar 18;15:290-298. doi: 10.1016/j.csbj.2017.03.002. eCollection 2017.
Identification of genetic polymorphisms and subsequent development of molecular markers is important for marker assisted breeding of superior cultivars of economically important species. Sweet cherry ( L.) is an economically important non-climacteric tree fruit crop in the Rosaceae family and has undergone a genetic bottleneck due to breeding, resulting in limited genetic diversity in the germplasm that is utilized for breeding new cultivars. Therefore, it is critical to recognize the best platforms for identifying genome-wide polymorphisms that can help identify, and consequently preserve, the diversity in a genetically constrained species. For the identification of polymorphisms in five closely related genotypes of sweet cherry, a gel-based approach (TRAP), reduced representation sequencing (TRAPseq), a 6k cherry SNParray, and whole genome sequencing (WGS) approaches were evaluated in the identification of genome-wide polymorphisms in sweet cherry cultivars. All platforms facilitated detection of polymorphisms among the genotypes with variable efficiency. In assessing multiple SNP detection platforms, this study has demonstrated that a combination of appropriate approaches is necessary for efficient polymorphism identification, especially between closely related cultivars of a species. The information generated in this study provides a valuable resource for future genetic and genomic studies in sweet cherry, and the insights gained from the evaluation of multiple approaches can be utilized for other closely related species with limited genetic diversity in the breeding germplasm.
鉴定遗传多态性并随后开发分子标记对于经济重要物种优良品种的标记辅助育种至关重要。甜樱桃(L.)是蔷薇科一种经济重要的非跃变型树果作物,由于育种导致经历了遗传瓶颈,使得用于培育新品种的种质遗传多样性有限。因此,识别用于鉴定全基因组多态性的最佳平台至关重要,这有助于识别并进而保护遗传受限物种的多样性。为了鉴定甜樱桃五个密切相关基因型中的多态性,对基于凝胶的方法(TRAP)、简化代表性测序(TRAPseq)、6k樱桃SNP阵列和全基因组测序(WGS)方法在甜樱桃品种全基因组多态性鉴定中的应用进行了评估。所有平台均以不同效率促进了基因型间多态性的检测。在评估多种SNP检测平台时,本研究表明,对于高效鉴定多态性,尤其是物种密切相关品种之间的多态性,需要结合适当的方法。本研究产生的信息为甜樱桃未来的遗传和基因组研究提供了宝贵资源,并且从多种方法评估中获得的见解可用于育种种质中遗传多样性有限的其他密切相关物种。