Roden Suzanne E, Dutton Peter H, Morin Phillip A
Southwest Fisheries Science Center, La Jolla, CA 92037, USA.
J Hered. 2009 May-Jun;100(3):390-3. doi: 10.1093/jhered/esn108. Epub 2008 Dec 12.
The green sea turtle, Chelonia mydas, was used as a case study for single nucleotide polymorphism (SNP) discovery in a species that has little genetic sequence information available. As green turtles have a complex population structure, additional nuclear markers other than microsatellites could add to our understanding of their complex life history. Amplified fragment length polymorphism technique was used to generate sets of random fragments of genomic DNA, which were then electrophoretically separated with precast gels, stained with SYBR green, excised, and directly sequenced. It was possible to perform this method without the use of polyacrylamide gels, radioactive or fluorescent labeled primers, or hybridization methods, reducing the time, expense, and safety hazards of SNP discovery. Within 13 loci, 2547 base pairs were screened, resulting in the discovery of 35 SNPs. Using this method, it was possible to yield a sufficient number of loci to screen for SNP markers without the availability of prior sequence information.
绿海龟(Chelonia mydas)被用作一个案例研究对象,用于在一个几乎没有可用遗传序列信息的物种中发现单核苷酸多态性(SNP)。由于绿海龟具有复杂的种群结构,除微卫星外的其他核标记可能会增进我们对其复杂生活史的理解。扩增片段长度多态性技术被用于生成基因组DNA的随机片段集,然后用预制凝胶进行电泳分离,用SYBR Green染色,切除并直接测序。不使用聚丙烯酰胺凝胶、放射性或荧光标记引物或杂交方法就可以执行此方法,从而减少了SNP发现的时间、费用和安全风险。在13个位点内,筛选了2547个碱基对,结果发现了35个SNP。使用这种方法,在没有先前序列信息的情况下,也有可能产生足够数量的位点来筛选SNP标记。