https://www.ahs.ac.cn/images/0513-353X/images/top-banner1.jpg|#|苹果
https://www.ahs.ac.cn/images/0513-353X/images/top-banner2.jpg|#|甘蓝
https://www.ahs.ac.cn/images/0513-353X/images/top-banner3.jpg|#|菊花
https://www.ahs.ac.cn/images/0513-353X/images/top-banner4.jpg|#|灵芝
https://www.ahs.ac.cn/images/0513-353X/images/top-banner5.jpg|#|桃
https://www.ahs.ac.cn/images/0513-353X/images/top-banner6.jpg|#|黄瓜
https://www.ahs.ac.cn/images/0513-353X/images/top-banner7.jpg|#|蝴蝶兰
https://www.ahs.ac.cn/images/0513-353X/images/top-banner8.jpg|#|樱桃
https://www.ahs.ac.cn/images/0513-353X/images/top-banner9.jpg|#|观赏荷花
https://www.ahs.ac.cn/images/0513-353X/images/top-banner10.jpg|#|菊花
https://www.ahs.ac.cn/images/0513-353X/images/top-banner11.jpg|#|月季
https://www.ahs.ac.cn/images/0513-353X/images/top-banner12.jpg|#|菊花

园艺学报 ›› 2014, Vol. 41 ›› Issue (7): 1361-1368.

• 蔬菜 • 上一篇    下一篇

利用小孢子培养创建大白菜—结球甘蓝易位系

胡永霞,李晓峰,轩淑欣,申书兴,王彦华*   

  1. 河北农业大学园艺学院,河北省蔬菜种质创新与利用重点实验室,河北保定 071001
  • 出版日期:2014-07-25 发布日期:2014-07-25
  • 基金资助:
    国家自然科学基金项目(31171964,31101552);‘十二五’农村领域国家科技计划项目(2012AA100102-5);农业科研杰出人才培养计划项目;河北省自然科学基金项目(C2010000677,C2014204093);高等学校博士学科点专项科研基金项目(20101302120006);河北省高等学校科学技术研究项目(Z2010149)

Obtaining of One Chinese Cabbage–Cabbage Translocation Line by Microspore Culture

HU Yong-xia,LI Xiao-feng,XUAN Shu-xin,SHEN Shu-xing,and WANG Yan-hua*   

  1. College of Horticulture,Agriculture University of Hebei,Key Laboratory for Vegetable Germplasm Enhancement and
    Utilization of Hebei,Baoding,Hebei 071001,China
  • Online:2014-07-25 Published:2014-07-25

摘要: 为创建大白菜—结球甘蓝易位系,以大白菜—结球甘蓝3 号单体异附加系(AA + C3)为试
材,进行了游离小孢子培养,利用结球甘蓝C02 连锁群相对于大白菜的特异InDel 标记对获得的小孢子植
株进行鉴定,从17 个小孢子植株中筛选出1 个具有结球甘蓝特异条带的植株。通过对InDel 标记的加密
设计,明确了该植株中外源甘蓝片段的大小为1.03 Mb。利用大白菜A 基因组10 个连锁群上均匀分布的
100 个InDel 标记对其进行分子鉴定,初步确定了该植株中甘蓝染色体片段位于大白菜5 号染色体上。花
粉母细胞减数分裂观察结果显示,该植株染色体数为20 条,为添加结球甘蓝3 号染色体片段的大白菜—
结球甘蓝易位系。

关键词: 大白菜, 结球甘蓝, 小孢子培养, 易位系, InDel标记

Abstract: In order to create Chinese cabbage–cabbage translocation lines,isolated microspores of Chinese cabbage–cabbage monosomic addition lines 3#(AA + C3)were cultured. Through identifying the obtained microspore plants by specific InDel markers located on Linkage group C02 of cabbage,one plant which has cabbage specific bands was identified from seventeen microspore plants. By designing multiple InDel markers around the targeted region,the exogenous cabbage fragment size is clarified as 1.03 Mb in this plant. Using one hundred InDel markers uniformly distributed on ten A genome linkage groups of Chinese cabbage,the chromosome fragment of cabbage was preliminary determined on the 5# chromosome of Chinese cabbage. Meiosis behavior of this translocation line showed that the chromosome number of this plant is twenty,which is identified as one translocation line introduced one segment of chromosome 3# in cabbage.

Key words: Chinese cabbage, cabbage, microspore culture, translocation line, InDel markers

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