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草业学报 ›› 2016, Vol. 25 ›› Issue (10): 124-131.DOI: 10.11686/cyxb2016097

• 研究论文 • 上一篇    下一篇

免预培养高效菊苣遗传转化方法

李小冬, 蔡璐, 李世歌, 莫本田, 韩永芬, 王小利*   

  1. 贵州省草业研究所, 贵州 贵阳 550006
  • 收稿日期:2016-03-09 出版日期:2016-10-20 发布日期:2016-10-20
  • 通讯作者: E-mail:wangxiaolizhenyuan@126.com
  • 作者简介:李小冬(1984-),男,湖南邵阳人,副研究员,博士。 E-mail:lixiaodongzl@163.com
  • 基金资助:
    贵州省联合基金“利用AtmiR156培育高产耐刈菊苣种子新材料”(黔科合J LKN[2013]04),贵州省农科院博士启动基金“四倍体菊苣种质创新应用研究”(黔农科院人才启动项目[2013]01)和农科院自主创新科研专项“贵州主要优良牧草种质资源发掘与创新利用研究”(黔农科院自主创新科研专项字[2014]010号)资助

An effective transformation method mediated by Agrobacterium in chicory (Cichorium intybus)

LI Xiao-Dong, CAI Lu, LI Shi-Ge, MO Ben-Tian, HAN Yong-Fen, WANG Xiao-Li*   

  1. Guizhou Institute of Prataculturae, Guiyang 550006, China
  • Received:2016-03-09 Online:2016-10-20 Published:2016-10-20

摘要: 转基因技术对基因功能研究与农作物种质资源创新具有重要作用,在牧草类作物菊苣中相应的研究还处于初级阶段。本研究改进了菊苣组织培养与遗传转化方法,采用暗光培养的菊苣子叶为外植体,经农杆菌侵染后置于光照条件下进行共培养,利用子叶细胞从暗光转移到光照条件下细胞迅速分裂的特点,实现植物遗传转化。与已报道的转化方法(光照条件下的真叶外植体先进行2~3 d预培养,再进行农杆菌转化与共培养)相比,本方法出苗率与已报道方法相当,达90%以上;比不经预培养方法的出苗率要高80%~90%,能极大节省人力物力。同时本研究发现,在愈伤诱导、植物分化以及生根培养中,依次递减细胞分裂素的强度与浓度,能显著降低愈伤和再生苗的玻璃化程度,与一直采用强细胞分裂素相比,改进方法愈伤玻璃化比率下降约9%,再生苗玻璃化比例下降约16%。

Abstract: Transgenic technology plays an important role in gene function analysis and crop germplasm innovation. However, transgenic studies are relatively recent in chicory. In this study we sought to improve tissue culture and genetic transformation methodology in chicory. Cotyledons grown in the dark were collected as explants. After transformation mediated by Agrobacteria, these explants were grown under illuminated conditions. The cotyledon cells divided rapidly when they were transferred from dark to light. The emergence rate of regenerated seedlings was greater than 90%, similar to that of previous studies however, the germination rate could be improved by 80%-90% if the explants were not pre-cultured. Our results were time, money and labor-saving. We also found that during callus induction, plant differentiation and root growth, decreased intensity and concentration of cytokinin significantly reduced the vitrification of callus and regenerated plantlets. Compared with continuously applied cytokinin our method decreased vitrification of callus and regenerated plantlets by about 9% and 16% respectively.