遗传 ›› 2010, Vol. 32 ›› Issue (7): 737-743.doi: 10.3724/SP.J.1005.2010.00737

• 研究报告 • 上一篇    下一篇

中国龙虾微卫星标记的筛选及遗传多样性分析

刘楚吾, 黎锦明, 刘丽, 郭昱嵩   

  1. 广东海洋大学水产学院, 南海水产经济动物增养殖广东普通高校重点实验室, 湛江 524025
  • 收稿日期:2009-10-11 修回日期:2010-02-07 出版日期:2010-07-20 发布日期:2010-07-20
  • 通讯作者: 刘楚吾 E-mail:swyjs@gdou.edu.cn
  • 基金资助:

    国家科技支撑计划项目(编号:2007BAD29B03)资助

Screening and genetic diversity analysis of microsatellite markers in Chinese lobster(Panulirus stimpsoni)

LIU Chu-Wu, LI Jin-Ming, LIU Li, GUO Yu-Song   

  1. Fisheries College, Key Laboratory of Aquaculture in South China Sea for Aquatic Economic Animal of Guangdong Higher Education Institutes, Guangdong Ocean University, Zhanjiang 524025, China
  • Received:2009-10-11 Revised:2010-02-07 Online:2010-07-20 Published:2010-07-20
  • Contact: LIU Chu-Wu E-mail:swyjs@gdou.edu.cn

摘要: 文章以M13通用引物和重复序列(CT)15、(AT)15引物, 利用PCR法对中国龙虾(Panulirus stimpsoni Hoehuis)部分基因组DNA文库进行筛选。共获得78个微卫星序列, 分别分布于55个阳性重组克隆中, 其中完美型(perfect)共50个, 占64%; 非完美型(imperfect)3个, 占3.8%; 混合完美型(compound perfect)6个, 占7.7%; 混合非完美型(compound imperfect)19个, 占24.5%。根据微卫星序列, 设计并筛选出15对微卫星多态性引物, 对中国龙虾的群体进行了遗传多样性分析。获得3~12个等位基因, 等位基因大小在78~425 bp之间, 基本符合引物设计的理论长度。期望杂合度范围为0.48~0.87, 平均值为0.71, 表明中国龙虾基因组微卫星具有较高的杂合度与遗传多样性。15个微卫星位点的PIC值从0.44到0.84, 平均值为0.60, 说明这些微卫星位点在中国龙虾基因组中包含丰富的遗传信息, 合适用于中国龙虾的各种分子标记及遗传学分析和应用。

关键词: 中国龙虾, 基因组文库, 微卫星标记, 遗传多样性, 引物筛选

Abstract: With the construction of a library of partial fractionated genomic DNA of Panulirus stimpsoni Hoehuis, the microsatellite sequences of P. stimpsoni were screened by PCR technique. Then, the genetic diversity was analyzed with the microsatellite markers. Seventy-eight microsatellite sequences in 55 positive recombinant clones were obtained by PCR technique with primers of M13+/- and (CT)15, and (AT)15. Among these microsatellite sequences, the numbers of perfect, imperfect, compound perfect, and compound imperfect sequences were 50 (64%), 3 (3.8%), 5 (7.7%), and 19 (24.5%), respectively. To analyze genomic DNA diversity of P. stimpsoni, 15 pairs of primers were designed from the microsatellite flanking sequences. In these microsatellite loci, the alleles numbers ranged from 3 to 12; and the sizes of these alleles ranged from 78 to 425 bp, which are in accordance with their predicted size range. The expected heterozygosity (He) and the polymorphism information content (PIC) ranged from 0.48 to 0.87 and 0.44 to 0.84 with the average values of 0.71 and 0.60, respectively. These results showed that these microsatellite loci were suitable for P. stimpsoni molecule markers and genetic analysis because of their richness in genetic information.

Key words: Panulirus stimpsoni, genomic library, microsatellite markers, genetic diversity, primer screen