一种适用于虾类育种项目中高通量基因分型的磁珠DNA提取方法

Q4 Agricultural and Biological Sciences Genetics of Aquatic Organisms Pub Date : 2019-12-02 DOI:10.4194/2459-1831-v3_2_02
Cheryl K. Y. Tan, J. Cowley, D. Jerry
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引用次数: 0

摘要

基于磁珠的核酸提取试剂盒由于其便利性,在对虾基因分型和病原体筛选中得到了广泛的应用。然而,在需要测试成千上万只虾的高级育种项目中,它们的成本可能令人望而却步。因此,评估了不同蛋白酶K消化,组织裂解和头洗涤缓冲液以及磁头类型的各种排列,以设计高通量虾DNA提取(SDE)方案,能够使用KingFisher™Flex磁颗粒处理器回收高纯度DNA。当使用MassARRAY®平台(Agena Bioscience)进行基因分型时,需要在单个多重PCR中共同扩增60-61个基因组区域,使用SDE协议或商业试剂盒从虾肌肉组织中提取的DNA产生可比的单核苷酸多态性(SNP)呼叫数据。SDE方案还从鲑鱼鳍夹中提取了高纯度的DNA。因此,它提供了显著降低虾和鲑鱼育种计划中大规模基因分型成本的潜力。
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A Magnetic Bead-Based DNA Extraction Protocol Suitable for High-Throughput Genotyping in Shrimp Breeding Programs
Due to their convenience, magnetic bead-based nucleic acid extraction kits are commonly used in shrimp genotyping and pathogen screening applications. However, in advanced breeding programs requiring the testing of many thousands of shrimp, their cost can be prohibitive. Various permutations of different Proteinase K digestion, tissue lysis and bead washing buffers as well as magnetic bead types were thus evaluated to devise a high-throughput shrimp DNA extraction (SDE) protocol capable of recovering high-purity DNA using a KingFisher™ Flex Magnetic Particle processor. When genotyped using a MassARRAY® platform (Agena Bioscience) requiring 60-61 genome regions to be co-amplified in a single multiplexed PCR, DNA extracted from shrimp muscle tissue using either the SDE protocol or a commercial kit generated comparable single-nucleotide polymorphism (SNP) call data. The SDE protocol also extracted high-purity DNA from salmon fin clips. It thus offers potential to markedly reduce the costs of large-scale genotyping in shrimp and salmon breeding programs.
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来源期刊
Genetics of Aquatic Organisms
Genetics of Aquatic Organisms Agricultural and Biological Sciences-Aquatic Science
CiteScore
0.90
自引率
0.00%
发文量
8
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