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植物研究 ›› 2017, Vol. 37 ›› Issue (3): 447-452.doi: 10.7525/j.issn.1673-5102.2017.03.016

• 研究报告 • 上一篇    下一篇

基于RAD-seq技术的异型花SSR信息分析

王久利1,2, 朱明星3, 徐明行3, 陈世龙1, 张发起1   

  1. 1. 中国科学院高原生物适应与进化重点实验室, 中国科学院西北高原生物研究所, 西北生态环境资源研究院, 西宁 810001;
    2. 中国科学院大学, 北京 100039;
    3. 青海大学生态环境工程学院, 西宁 810016
  • 收稿日期:2016-12-26 出版日期:2017-05-15 发布日期:2017-06-03
  • 通讯作者: 张发起,E-mail:fqzhang@nwipb.cas.cn E-mail:fqzhang@nwipb.cas.cn
  • 作者简介:王久利(1991-),男,博士研究生,主要从事植物学方面的研究。
  • 基金资助:
    国家自然科学基金(31400322);青海省应用基础研究计划(2016-ZJ-761)

Analysis on SSR in Sinoswertia tetraptera Base on RAD-seq

WANG Jiu-Li1,2, ZHU Ming-Xing3, XU Ming-Hang3, CHEN Shi-Long1, ZHANG Fa-Qi1   

  1. 1. Key Laboratory of Adaptation and Evolution of Plateau Biota, Northwest Institute of Plateau Biology, Northwest Institute of Eco-Environment and Resources, Chinese Academy of Sciences, Xining 810008;
    2. University of the Chinese Academy of Sciences, Beijing 100039;
    3. College of Ecology-Environment Engineering, Qinghai University, Xining 810016
  • Received:2016-12-26 Online:2017-05-15 Published:2017-06-03
  • Supported by:
    National Natural Science Foundation of China(31400322);Applied Basic Research Programs of Qinghai Province(2016-ZJ-761)

摘要: 用RAD-seq(restriction-site associated DNA sequencing)对异型花(Sinoswertia tetraptera(Maxiowicz) T.N.Ho,S.W.Liu & J.Q.Liu)进行简化基因组测序,并借此分析异型花的SSR(simple sequence repeats)信息。利用SR search软件甄别所得序列中的SSR,得到了双端各有至少100 bp的SSR位点5 844个,其中5 339个(91.38%)成功设计引物,而三核苷酸SSR位点最多(3 323个);在能成功设计引物的SSR位点中,重复序列长度包括17种(12~36 bp);重复序列的基序共277种,其中五核苷酸基序种类最多(106种);随机挑选10对SSR引物,用4个异型花居群的32个个体检测检测其可用性和多态性,经PCR和聚丙烯酰氨凝胶电泳检测,有4对(ST2、ST3、ST6和ST10)成功扩增并表现出多态性;经GENEPOP 4.4对4个位点分析,显示其等位基因数量均值为6,多态性较高且不连锁(P<0.01);4个位点在多数居群中偏离哈迪温伯格平衡(P<0.01)且存在较高的纯合子数量(观测杂合度均值0.023),该结果归因于异型花主要进行自花授粉,在自然界中很难形成进行自由交配的居群;此外,ST2和ST6可在椭圆叶花锚(Halenia elliptica D.Don)中成功扩增,具有潜在通用性。本研究将为日后基于异型花SSR标记的相关研究提供数据库支持。

关键词: RAD-seq, 简化基因组测序, 异型花, SSR, 獐牙菜亚族

Abstract: We used the restriction-site associated DNA sequencing(RAD-seq) technology to analyze simple sequence repeats(SSR) information of Sinoswertia tetraptera(Maxiowicz) T.N.Ho, S.W.Liu & J.Q.Liu. The 5844 SSR loci, with at least 100 bp at two ends, were identified using SR search software. The 5339(91.38%) loci's primers were designed successfully. Among which, amount of tri-nucleotide SSR loci is the most(3323); repeat sequence length type number is 17, while repeat motif type number is 227, and type number of penta-nucleotide motif is the most(106). We employed 32 individuals from 4 natural populations of S.tetraptera to estimate usability and polymorphism of 10 pairs of SSR primers selected randomly from the 5 339 pairs of primers. According to the result of PCR and Polyacrylamide gel electrophoresis, four pairs of primers(ST2, ST3, ST6 and ST10) amplified favorably and showed polymorphism. By the GENEPOP 4.4, the mean number of alleles of the four loci is 6; these loci do not link to each other(P<0.01); these loci deviate from HWE(P<0.01) in most populations and have many homozygotes(observed heterozygosity mean 0.023), which due to the cleistogamous pollination mode of S.tetraptera. ST2 and ST6 were successfully amplified in Halenia elliptica. Our study will offer a SSR dataset in the future based on SSR markers of S.tetraptera.

Key words: RAD-seq, reduced-representation sequencing, Sinoswertia tetraptera, SSR, subtribe Swertiinae

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