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植物研究 ›› 2016, Vol. 36 ›› Issue (6): 860-869.doi: 10.7525/j.issn.1673-5102.2016.06.009

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橡胶树MSAP反应体系优化及其不同开割高度单株DNA甲基化分析

吴春太1, 班硕1,2, 黎瑜1, 曾日中1   

  1. 1. 中国热带农业科学院橡胶研究所/农业部橡胶树生物学与遗传资源利用重点实验室/国家橡胶树育种中心/海南省热带作物栽培生理学重点实验室, 儋州 571737;
    2. 华中农业大学植物科学技术学院, 武汉 430070
  • 收稿日期:2016-03-25 出版日期:2016-11-15 发布日期:2016-11-16
  • 通讯作者: 曾日中,E-mail:hnzrz@aliyun.com E-mail:hnzrz@aliyun.com
  • 作者简介:吴春太(1972-),男,博士,副研究员,主要从事橡胶树产胶特性研究。
  • 基金资助:
    国家自然科学基金资助项目(31270713);橡胶研究所基本科研业务费资助项目(1630022012008)

Optimization of MSAP Analysis System for Hevea brasiliensis and Its Application in Plant of Different Heights of Opening for Tapping

WU Chun-Tai1, BAN Shuo1,2, LI Yu1, ZENG Ri-Zhong1   

  1. 1. Rubber Research Institute, Chinese Academy of Tropical Agriculture Sciences/Key Laboratory of Biology and Genetic Resources of Rubber Tree, Ministry of Agriculture, the People's Republican of China/State Center for Rubber Breeding/Hainan Provincial Key Laboratory of Physiology for Tropical Crops, Danzhou 571737;
    2. College of Plant Science and Technology, Huazhong Agricultural University, Hubei, Wuhan 430070
  • Received:2016-03-25 Online:2016-11-15 Published:2016-11-16
  • Supported by:
    National Natural Science Foundation of China(No.31270713);Fundamental Research Funds for Rubber Research Institute,CATAS(No.1630022012008)

摘要: 以‘热研7-33-97’橡胶树无性系幼嫩叶片为材料,通过利用单因素和正交试验相结合的方法,对酶切、预扩增和选择性扩增3个影响甲基化敏感扩增多态性(MSAP)分析的关键步骤的反应体系中关键影响因素进行了优化,建立橡胶树MSAP反应最佳体系,并用于高低割线橡胶树基因组DNA甲基化差异分析。结果表明:在50 μL反应体系中,750 ng基因组DNA用EcoRⅠ 20 U,HpaⅡ 20 U或MspⅠ 10 U于37℃恒温同步酶切10 h,酶切完全。最佳预扩增体系(20 μL)为:连接产物4 μL,MgCl2(25 mmol·L-1)0.15 μL,dNTPs(2.5 mmol·L-1)0.1 μL,上下游引物E-00/HM-00(10 μmol·L-1)各0.3 μL,Taq酶(5 U·μL-1)0.1 μL,10×PCR Buffer 2 μL。最佳选择性扩增反应体系(20 μL)为:稀释20倍的预扩增产物2 μL,MgCl2(25 mmol·L-1)0.1 μL,dNTPs(2.5 mmol·L-1)0.125 μL,上下游引物E+3/HM+3(10 μmol·L-1)各0.4 μL,Taq酶(5 U·μL-1)0.1 μL,10×PCR Buffer 2 μL。高低割线树DNA的甲基化比例分别为37.22%和36.43%,2种开割胶树基因组CCGG位点胞嘧啶全甲基化率明显高于半甲基化率,推测橡胶树基因组甲基化主要模式可能是CpG型。综上表明,建立的MSAP反应体系稳定可靠且重复性好,为后续橡胶树不同胁迫(割胶)程度DNA甲基化的研究奠定了基础。

关键词: 高低割线橡胶树, DNA甲基化, 甲基化敏感扩增多态性(MSAP), 体系优化

Abstract: Using the tender leaves of Hevea brasiliensis variety‘CATAS 7-33-97’as materials, several key influencing factors in leaf genomic DNA restriction enzyme digestion, pre-amplification and selective amplification system which affected the system quality of MSAP were optimized through the single factor and orthogonal design method in order to obtain the optimal MSAP reaction system of rubber tree. The optimized reaction system of MSAP was used for difference analysis of DNA methylation in two kinds of H.brasiliensis of high and low tapping cuts. The results showed that 750 ng genomic DNA in a reaction volume of 50 μL could be fully digested by EcoRⅠ 20 U, HpaⅡ 20 U or MspⅠ 10 U at 37℃ for 10 h. MSAP-PCR pre-amplification was performed in 20 μL of reaction volume with the following mix:ligation products 4 μL, MgCl2(25 mmol·L-1)0.15 μL, dNTPs(2.5 mmol·L-1)0.1 μL, Taq polymerase(5 U·μL-1) 0.1 μL, 10×PCR Buffer 2 μL, primer E-00/HM-00(10 μmol·L-1) 0.3 μL, respectively. The 20 μL selective reaction mixture contained 20 times diluted amplification products 2 μL, MgCl2(25 mmol·L-1) 0.1 μL, dNTPs(2.5 mmol·L-1) 0.125 μL, Taq polymerase(5 U·μL-1) 0.1 μL, 10×PCR Buffer 2 μL, primer E+3/HM+3(10 μmol·L-1) 0.4 μL respectively. The total methylation rates of two samples were 37.22% and 36.43%, respectively. The full methylation rates were more than the hemi-methylation rates in H.brasiliensis of different tapping cuts. Therefore, CpG methylation may represent the major form of DNA methylation in rubber tree. Our data indicated that this MSAP reaction system with high stability and reliablity and good reproducibility have provided the foundation for different degree tapping stress of rubber tree associated research with the MSAP technology.

Key words: Hevea brasiliensis of high and low tapping cuts, DNA methylation, methylation sensitive amplified polymorphism(MSAP), system optimization

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