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稻瘟病抗性基因Pi-d2、Pi-d3和Pigm不同敲除突变体的抗性评价

张柱坚 陈子强 顾建强 田大刚

张柱坚, 陈子强, 顾建强, 田大刚. 稻瘟病抗性基因Pi-d2、Pi-d3和Pigm不同敲除突变体的抗性评价[J]. 福建农业学报, 2018, 33(12): 1231-1236. doi: 10.19303/j.issn.1008-0384.2018.12.001
引用本文: 张柱坚, 陈子强, 顾建强, 田大刚. 稻瘟病抗性基因Pi-d2、Pi-d3和Pigm不同敲除突变体的抗性评价[J]. 福建农业学报, 2018, 33(12): 1231-1236. doi: 10.19303/j.issn.1008-0384.2018.12.001
ZHANG Zhu-jian, CHEN Zi-qiang, GU Jian-qiang, TIAN Da-gang. Resistance on Rice Blast of Knockout Mutants of Pi-d2, Pi-d3 and Pigm[J]. Fujian Journal of Agricultural Sciences, 2018, 33(12): 1231-1236. doi: 10.19303/j.issn.1008-0384.2018.12.001
Citation: ZHANG Zhu-jian, CHEN Zi-qiang, GU Jian-qiang, TIAN Da-gang. Resistance on Rice Blast of Knockout Mutants of Pi-d2, Pi-d3 and Pigm[J]. Fujian Journal of Agricultural Sciences, 2018, 33(12): 1231-1236. doi: 10.19303/j.issn.1008-0384.2018.12.001

稻瘟病抗性基因Pi-d2、Pi-d3和Pigm不同敲除突变体的抗性评价

doi: 10.19303/j.issn.1008-0384.2018.12.001
基金项目: 

福建省科技计划项目——省属公益类科研院所基本科研专项 2017R1019-10

福建省科技计划项目——省属公益类科研院所基本科研专项 2018R1019-9

详细信息
    作者简介:

    张柱坚(1994-), 男, 硕士研究生, 研究方向:分子植物育种(E-mail:723926289@qq.com)

    通讯作者:

    田大刚(1978-), 男, 副研究员, 研究方向:水稻分子免疫和抗病育种(E-mail:tdg@fjage.org)

  • 中图分类号: S511

Resistance on Rice Blast of Knockout Mutants of Pi-d2, Pi-d3 and Pigm

  • 摘要: 谷丰B是一个广谱高抗稻瘟病水稻保持系,含有稻瘟病抗性基因Pi-d2,Pi-d3和Pigm。为了进一步明确3个抗性基因在谷丰B中的作用,本研究利用CRISPR/Cas9多基因编辑系统构建了共敲除Pi-d2+Pi-d3+Pigm基因载体。通过遗传转化试验以及DNA测序,T0代植株获得多种突变体组合类型。对其中的Pi-d2、PigmPi-d2+Pi-d3、Pi-d2+PigmPi-d2+Pi-d3+Pigm等5种纯合突变体的T1代株系进行稻瘟病室内接种鉴定,研究结果表明,Pi-d2、Pi-d3和Pigm分别对86/501-3、KJ201/CHE86061和86/CHE86061/501-3的菌株存在显著的抗性效应,Pi-d2+Pi-d3,Pi-d2+PigmPi-d2+Pi-d3+Pigm的敲除株系的抗性不完全等同于单个基因的简单叠加,其中Pi-d2+Pi-d3+Pigm的突变体对菌株CHL768表现完全不同于其他类型突变体的感病性。上述结果为解析广谱高抗稻瘟病水稻材料谷丰B的抗性遗传机理提供重要信息,也为水稻稻瘟病抗病育种研究提供参考。
  • 图  1  PigmPi-d2和Pi-d3多基因编辑载体构建

    注:(A)PigmPi-d2和Pi-d3多基因编辑载体结构。(B)gRNA表达盒电泳检测。M为DL 2 000 Plus DNA Marker;1为u6b-Pigm-gRNA表达盒;2为u6a-Pi-d2-gRNA表达盒;3为u6b-Pi-d2-gRNA表达盒;4为u6a-Pi-d3-gRNA表达盒;5为u6b-Pi-d2-gRNA表达盒。(C)PigmPi-d2和Pi-d3多基因编辑载体菌落PCR检测。M为DL 2 000 Plus DNA Marker;1为不含模板的空白对照;2~11为单菌落PCR产物。

    Figure  1.  Construction of Pigm, Pi-d2 and Pi-d3 multi-gene editing vectors

    图  2  靶位点突变序列分析

    注:(A)PCR鉴定转基因阳性株系。M为DL 2 000 Plus DNA Marker;1为阳性对照;2为不含模板的空白对照;3为以野生型谷丰B植株DNA为模板的PCR产物;4~23为以阳性苗DNA为模板的PCR产物。(B)T0代纯合突变类型分析结果。下划线部分为PAM区;横线为碱基缺失,箭头为碱基插入。(C)T1代植株突变类型测序结果。下划线部分为PAM区。

    Figure  2.  Analysis on mutation sequences of target spots

    表  1  本研究所用的引物

    Table  1.   Primers applied

    引物名称 引物序列 用途
    Pigm-u6b-F GTTGGATACGGATAGCGATCCGG 构建Pigm敲除载体
    Pigm-u6b-R AAACCCGGATCGCTATCCGTATC
    Pi-d2-u6a-F GCCGAAGTCATCTGAATGGGTGAC 构建Pi-d2敲除载体
    Pi-d2-u6a-R AAACGTCACCCATTCAGATGACTT
    Pi-d2-u6b-F GTTGAATGCCTTCCTGCAGTCAGG 构建Pi-d2敲除载体
    Pi-d2-u6b-R AAACCCTGACTGCAGGAAGGCATT
    Pi-d3-u6a-F GCCGCCTCTTTTCTGAGATCCGGG 构建Pi-d3敲除载体
    Pi-d3-u6a-R AAACCCCGGATCTCAGAAAAGAGG
    Pi-d3-u6b-F GTTGCCGCGTTCGTCAAGCAGGTG 构建Pi-d3敲除载体
    Pi-d3-u6b-R AAACCACCTGCTTGACGAACGCGG
    Cas9-Pigm-F GAAAGACGAACTATTAAAGG Pigm敲除载体测序鉴定
    Cas9-Pigm-R TGATCCAGAGAACTGGGGCC
    Cas9-Pi-d2-F GCTCTGTCTTTGGCTTTGGT Pi-d2敲除载体测序鉴定
    Cas9-Pi-d2-R GCTCTGTCTTTGGCTTTGGT
    Cas9-Pi-d3-F GTGTTGTGGGCTCACTAATC Pi-d3敲除载体测序鉴定
    Cas9-Pi-d3-R CAGCAAATCCCTCTTCTTCT
    HPT-F AAGCTGCATCATCGAAATTG 潮霉素鉴定
    HPT-R TCGTTATGTTTATCGGCACT
    下载: 导出CSV

    表  2  突变株系与对照株系的稻瘟病抗性鉴定结果

    Table  2.   Blast-resistance of mutant and control lines as evaluated by fungal inoculation

    材料抗性等级 菌株
    KJ201 86 CHE86061 501-3 CHL768 CHL2110
    谷丰B 0 0 0 0 0 4
    GFB234-5(Pi-d2) 0 3 0 5 0 4
    GFB234-3(Pigm) 0 4 5 5 0 4
    GFB234-11(Pi-d2+ Pi-d3) 2 3 4 5 0 4
    GFB234-8(Pigm+ Pi-d3) 1 4 4 5 0 4
    GFB234-15(Pigm+Pi-d2+ Pi-d3) 4 4 4 5 3 4
    下载: 导出CSV
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  • 收稿日期:  2018-11-13
  • 修回日期:  2018-12-10
  • 刊出日期:  2018-12-28

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