华北农学报 ›› 2017, Vol. 32 ›› Issue (6): 67-72. doi: 10.7668/hbnxb.2017.06.010

所属专题: 白菜 生物技术

• 论文 • 上一篇    下一篇

大白菜基因组DNA快速提取方法的研究

王涛1, 王超楠2, 张红2, 温娟娟1, 张斌2   

  1. 1. 天津师范大学 生命科学学院, 天津 300387;
    2. 天津科润蔬菜研究所, 蔬菜种质创新国家重点实验室, 天津市蔬菜遗传育种企业重点实验室, 天津 300381
  • 收稿日期:2017-07-18 出版日期:2017-12-28
  • 通讯作者: 张斌(1965-),男,辽宁本溪人,研究员,博士,主要从事十字花科蔬菜育种研究。
  • 作者简介:王涛(1992-),男,山西长治人,在读硕士,主要从事大白菜分子育种研究。
  • 基金资助:
    国家重点研发计划项目(2017YFD0101801);天津市自然科学基金项目(16JCYBJC29300);国家重点研发计划项目(2016YFD0101701);天津市现代农业产业技术体系创新团队建设专项计划(ITTVRS2017003);国家大宗蔬菜产业技术体系(CARS-25-G-02);天津市科技计划项目(16PTSYJC00260)

Study on Rapid Extraction of Genomic DNA from Chinese Cabbage

WANG Tao1, WANG Chaonan2, ZHANG Hong2, WEN Juanjuan1, ZHANG Bin2   

  1. 1. College of Life Sciences, Tianjin Normal University, Tianjin 300387, China;
    2. Tianjin Kernel Vegetable Research Institute, State Key Laboratory of Vegetable Germplasm Innovation, Key Laboratory of Tianjin Vegetable Genetic and Breeding Enterprises, Tianjin 300381, China
  • Received:2017-07-18 Published:2017-12-28

摘要: 快速高效的DNA提取是作物大规模分子育种的关键一步。旨为构建一种快速提取大白菜基因组DNA的方法,以大白菜叶片为试验材料,比较了CTAB法、二步CTAB法以及4种碱裂解法提取DNA的质量,分析了不同方法提取的DNA为模板的PCR扩增效果,还对不同方法提取的基因组DNA的保存时间和保存条件进行了比较,选择最优的方法在抗根肿病基因分子标记辅助选择中进行了应用。结果表明,CTAB法和3种碱裂解法提取的基因组DNA作为模板的PCR扩增产物,都可以通过8%的非变性聚丙烯酰胺凝胶电泳检测到清晰的条带。其中碱裂解法Ⅲ,不仅提取质量好,而且提取过程简单、快速,能够满足大白菜高通量DNA提取的需要,提取的DNA在4℃和-20℃的条件下保存,将保存至30 d的基因组DNA作为模板进行PCR扩增,产物仍然可以通过聚丙烯酰胺凝胶电泳检测到清晰的条带,说明这种方法保存时间较长,经验证,该方法在抗根肿病基因分子标记辅助选择中的应用效果也较好。碱裂解法Ⅲ显著提高了大白菜分子标记辅助筛选的效率,可广泛应用于大白菜分子标记辅助选择育种。

关键词: 大白菜, 基因组DNA, 快速提取

Abstract: Rapid and efficient DNA extraction is the key step in large-scale molecular breeding of crop. To construct a method for rapid extraction of genomic DNA from Chinese cabbage, the Chinese cabbage leaves were used as experimental materials, the quality of DNA extracted by the CTAB method, two-step CTAB method and four alkaline lysis methods was compared, the PCR amplification effects of DNA extracted by different methods were analyzed, and the preservation time and preservation conditions of genomic DNA extracted by different methods were compared, the optimal method was selected for the application of molecular marker-assisted selection against clubroot disease.The results showed that genomic DNA extracted by the CTAB and three kinds of alkaline lysis methods could be used as a template for PCR, and the PCR amplification products could be detected by 8% non-denaturing polyacrylamide gel electrophoresis to clear bands. Among them, the alkaline lysis method Ⅲ, not only the extraction quality was good and the extraction process was simple and fast, but also it could meet the needs of high-throughput DNA extraction of Chinese cabbage, the extracted DNA was stored at 4℃ and -20℃, and the genomic DNA stored for 30 days was used as a template for PCR amplification, the products was still detected by polyacrylamide gel electrophoresis to clear bands, it illustrates that this method has a long preservation time and it has been proved that this method has a good effect on the application of molecular marker-assisted selection against clubroot disease. Alkaline lysis method Ⅲ has significantly improved the efficiency of Chinese cabbage molecular marker-assisted selection, and can be widely used in Chinese cabbage molecular marker-assisted selection breeding.

Key words: Chinese cabbage, Genomic DNA, Rapid extraction

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引用本文

王涛, 王超楠, 张红, 温娟娟, 张斌. 大白菜基因组DNA快速提取方法的研究[J]. 华北农学报, 2017, 32(6): 67-72. doi: 10.7668/hbnxb.2017.06.010.

WANG Tao, WANG Chaonan, ZHANG Hong, WEN Juanjuan, ZHANG Bin. Study on Rapid Extraction of Genomic DNA from Chinese Cabbage[J]. ACTA AGRICULTURAE BOREALI-SINICA, 2017, 32(6): 67-72. doi: 10.7668/hbnxb.2017.06.010.

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