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| 基于Roche 454 GS FLX的钝吻黄盖鲽(Pleuronectes yokohamae)微卫星标记的开发 |
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潘 婷1,2, 张 岩3, 张辉4, 高天翔5, 肖永双4, 姜云荣1,2
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1. 上海海洋大学水产与生命学院 上海 201306;2. 农业部海洋渔业可持续发展重点实验室
中国水产科学研究院黄海水产研究所 青岛 266071;3.农业部海洋渔业可持续发展重点实验室
中国水产科学研究院黄海水产研究所 青岛 266071;4.中国科学院海洋研究所 青岛 266071;5.中国海洋大学水产学院 青岛 266003
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| 摘要: |
| 利用Roche 454 GS FLX平台测序技术进行了钝吻黄盖鲽微卫星引物筛选，并采用聚类分析的方法对得到的5641个微卫星位点进行类比分析，得到247种多态性位点，其中完美型占52.22%，非完美型占20.24%，复合型占27.54%，(AC)n、(AG)n两碱基重复类型的比例是44%，重复次数在10次以上的占总数的87.5%。随机选取11个位点的微卫星引物，采用5个野生个体，利用荧光标记和毛细管电泳进行多样性评价，4个位点偏离Hardy-Weinberg平衡，不同位点得到的等位基因范围为3−8，平均等位基因数为5.0。平均观望杂合度(Ho)、平均期望杂合度(He)及平均多态性信息含量(PIC)分别为0.588、0.788和0.670。结果表明，454 GS FLX提供了一种直观、高效开发微卫星的方法。 |
| 关键词: Roche 454 GS FLX 钝吻黄盖鲽 开发 微卫星标记 |
| DOI：10.11758/yykxjz.20150104 |
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| 基金项目:国家科技基础条件平台项目(2006DKA30470-006)资助 |
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| Microsatellite Loci Isolated by Roche 454 GS FLX in Pleuronectes yokohamae |
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| Abstract: |
| Roche 454 GS FLX, the second-generation sequencing technique, can read longer fragments accurately and isolate SSR markers, and thus has been widely used in many fields of research. In this study, we applied Roche 454 GS FLX to isolate the microsatellite loci and developed the identification of microsatellites markers in Pleuronectes yokohamae. (AC)12, (AG)12, (AAT)12, (AGG)8, (AGC)8, (AGAT)8 and (ACAG)6 were hybridized with shotgun library of DNA samples. This SSR library was constructed through magnetic beads enrichment, cleaning, elution and purification. The SSR library was then sequenced with Roche 454 GS FLX. MISA was used to search for microsatellite motifs and primer 3 was used to design the primers for P. yokohamae. FAM, HEX, and TAMRA were used to label the microsatellite primers (5′), which were used in the triplex PCR or the nested PCR to identify the genotype of the microsatellite loci. The cluster similarity comparison method was first used to analyze 5641 loci that we obtained, and 247 types of loci with high polymorphism were screened. Among these loci, 52.22% were perfect, 20.24% were imperfect and the rest 27.54% were compound. The percentage of (AC)n and (AG)n was 44% in these loci, and 87.5% of them were more than 10-time repeats. Eleven pairs of fluorescent primers were designed according to the selected loci (more than 10-time repeats) and were applied in 5 individuals. The number of alleles per locus ranged from 3 to 8 with an average value of 5. The average values of Ho, He and PIC were 0.588, 0.788 and 0.670 respectively. Four loci among 11 deviated from Hardy-Weinberg. The results of this research indicated that 454 GS FLX was an intuitive and efficient technique for microsatellite isolating. Our study provides essential information about the population genetic diversity of P. yokohamae, and helps improve the artificial breeding. |
| Key words: Roche 454 GS FLX Pleuronectes yokohamae Isolating Microsatellite markers |