中国农业科学 ›› 2013, Vol. 46 ›› Issue (18): 3750-3757.doi: 10.3864/j.issn.0578-1752.2013.18.002

• 作物遗传育种·种质资源·分子遗传学 • 上一篇    下一篇

应用ihpRNA干扰技术创制高支链淀粉马铃薯材料

 刘玉汇12, 王丽3, 杨宏羽1, 余斌12, 李元铭4, 张俊莲12, 王蒂12   

  1. 1.甘肃农业大学农学院/甘肃省作物遗传改良与种质创新重点实验室,兰州730070
    2.甘肃省干旱生境作物学重点实验室,兰州730070
    3.甘肃农业大学生命科学技术学院,兰州730070
    4.甘肃农村发展研究院,兰州730070
  • 收稿日期:2013-03-13 出版日期:2013-09-15 发布日期:2013-06-03
  • 通讯作者: 通信作者张俊莲,Tel:0931-7632021;E-mail:zhangjl@gsau.edu.cn。通信作者王蒂,Tel:0931-7632021;E-mail:wangd@gsau.edu.cn
  • 作者简介:刘玉汇,Tel:0931-7632021;E-mail:lyhui@aliyun.com
  • 基金资助:

    国家“十二五”科技支撑计划(2012BAD06B03)、国家现代农业产业技术体系建设项目(CARS-10-P18)、甘肃省育种专项(gsyzzx-1)、甘肃农业大学盛彤笙科技创新基金(GSAU-STS-1341)

Prodution of High-Amylopectin Potato Plants by Using ihpRNAi Technology

 LIU  Yu-Hui-12, WANG  Li-3, YANG  Hong-Yu-1, YU  Bin-12, LI  Yuan-Ming-4, ZHANG  Jun-Lian-12, WANG  Di-12   

  1. 1.College of Agronomy, Gansu Agricultural University/Gansu Key Laboratory of Crop Genetic and Germplasm Enhancement, Lanzhou 730070
    2.Gansu Key Laboratory of Aridland Crop Science, Lanzhou 730070
    3.College of Life Sciences and Technology, Gansu Agricultural University, Lanzhou 730070
    4.Gansu Rural Development Research Institute, Lanzhou 730070
  • Received:2013-03-13 Online:2013-09-15 Published:2013-06-03

摘要: 【目的】创造块茎高支链淀粉或纯支链淀粉含量的转基因马铃薯材料。【方法】以构建的由Patatin启动子驱动的pBI121g-PgABI为干扰表达载体,采用农杆菌介导法转化马铃薯优良品种甘农薯2号。用PCR、Southern blotting、半定量RT-PCR和实时荧光定量PCR技术检测转基因植株,并对转基因植株的微型薯进行淀粉含量的测定。【结果】通过农杆菌介导法获得10个转基因株系。PCR和Southern杂交结果证明,目的基因已被整合到基因组中,通过半定量RT-PCR分析表明,转基因株系中GBSSI的表达均受到明显抑制,且在6个转基因株系中检测不到mRNA的表达。进一步通过real-time PCR分析表明,转基因株系中GBSSI的mRNA沉默效率为66.27%—93.53%;转基因株系微型薯的淀粉含量也发生明显变化,其支链淀粉含量高达90.16%—98.84%,比对照高出10.31%—20.92%。转基因株系GBSSI的mRNA沉默效率与支链淀粉含量呈显著正相关(r=0.937,P<0.01)。【结论】采用ihpRNAi技术可有效抑制马铃薯块茎中内源GBSSI表达,获得高支链或纯支链淀粉含量的马铃薯材料。

关键词: 马铃薯 , 高支链淀粉 , ihpRNA干扰技术 , 颗粒结合型淀粉合成酶

Abstract: 【Objective】 The objective of this study is to develop transgenic potato (Solanum tuberosum L.) plants with high-amylopectin starch in its tubers.【Method】RNA interference expression vector pBI121g-PgABI driven by Patatin was transformed into elite potato cultivar ‘Gannongshu 2’ by Agrobacterium-mediated transformation. The transgenic plants were identified by PCR, Southern-blotting, semi-quantitative RT-PCR and real-time quantitative PCR and the starch content of transgenic potatoes was determined.【Result】Ten transgenic potato lines were confirmed by PCR and Southern blot analysis that the target gene integrated into the plant genomes. Result of semi-quantitative RT-PCR indicated that the accumulation of mRNAs derived from GBSSI was inhibited significantly in all transgenic lines, which were not detectable in 6 tansgenic lines. Result of real-time quantitative PCR showed that the inhibition ratio was 66.27%-93.53%. There were significant changes of starch content in ten transgenic microtubers,of which the amylopectin content was up to 90.16%-98.84%, 10.31%-20.92% higher than the non-transgenic microtuber. A significant correlation was found between inhibition ratio of mRNA and amylopectin content of transgenic potato plants (r=0.937, P<0.01). 【Conclusion】ihpRNAi technology can be used effectively in the production of high-amylopectin potato or pure-amylopectin potato by silencing endogenesis gene GBSSI.

Key words: potato (Solanum tuberosum L.) , high-amylopectin starch , ihpRNAi , granule-bound starch synthase