生物技术通报 ›› 2025, Vol. 41 ›› Issue (4): 106-114.doi: 10.13560/j.cnki.biotech.bull.1985.2024-0780

• 研究报告 • 上一篇    

利用单碱基基因编辑技术创制OsALS抗除草剂水稻种质资源

陈晓军1(), 惠建1, 马洪文2, 白海波1, 钟楠1, 李稼润1, 樊云芳3   

  1. 1.宁夏农林科学院农业生物技术研究中心 宁夏农业生物技术重点实验室,银川 750002
    2.宁夏农林科学院农作物研究所,银川 750002
    3.宁夏农林科学院枸杞科学研究所,银川 750002
  • 收稿日期:2024-08-14 出版日期:2025-04-26 发布日期:2025-04-25
  • 作者简介:陈晓军,博士,副研究员,研究方向 :植物分子生物学;E-mail: smallgene@126.com;陈晓军同为本文
  • 基金资助:
    宁夏回族自治区自然科学基金重点项目(2022AAC02052);国家自然科学基金区域创新发展联合基金(U23A20179);宁夏农业科技自主创新专项科技创新引导项目(NKY-22-02);宁夏回族自治区重点研发计划(2024BBF02002)

Creating Rice Gerplasm Resources OsALS Rsistant to Herbicide through Single Base Gene Editing Technology

CHEN Xiao-jun1(), HUI Jian1, MA Hong-wen2, BAI Hai-Bo1, ZHONG Nan1, LI Jia-run1, FAN Yun-fang3   

  1. 1.Agricultural Biotechnology Center, Ningxia Academy of Agriculture and Forestry Sciences/Key Lab of Agricultural Biotechnology of Ningxia, Yinchuan 750002
    2.Institute of Crop Science, Ningxia Academy of Agriculture and Forestry Sciences, Yinchuan 750002
    3.Institute of Wolfberry Science, Ningxia Academy of Agriculture and Forestry Sciences, Yinchuan 750002
  • Received:2024-08-14 Published:2025-04-26 Online:2025-04-25

摘要:

目的 以宁夏耐盐品种宁粳56为实验材料,定点编辑乙酰乳酸合酶ALS基因,创制具有抗除草剂特性的耐盐水稻新种质资源。 方法ALS基因171和190两个位点为靶位点,利用胞嘧啶碱基编辑器BE3,构建单碱基编辑载体OsALS171-SpG-eBE3和OsALS190-SpG-eBE3,通过农杆菌介导进行受体材料的基因转化获得基因编辑植株,采用靶位点测序的方法进行基因型鉴定;建立了除草剂耐受系统并对其除草剂的耐受程度进行了快速鉴定。 结果 经T1代靶位点测序验证,获得ALSP171F 2个突变纯合株系;ALSE187K R190HALSE187KALSV188IALSR190HALSD201N 5种突变类型纯合株系各1株。相对野生型受体材料,ALSP171F 2个突变纯合株系对双草醚有较强的耐受力,而ALSE187K R190HALSE187KALSV188IALSR190HALSD201N 5种突变纯合植株虽然对双草醚有一定的耐受,但耐受程度不显著。 结论 利用SpG胞嘧啶碱基编辑器BE3获得具有抗草剂特性的基因编辑材料,且能够稳定遗传,ALSP171F位点突变对双草醚除草剂表现较强抗性,是培育抗除草剂水稻的优先位点。

关键词: 水稻, 单碱基基因编辑, 抗除草剂, 乙酰乳酸合成酶

Abstract:

Objective This study edited the acetyl lactate synthase (ALS) gene at designated locus of Ningjing 56, Ningxia salt-tolerant variety, and created rice germplasm resources with herbicide resistance characteristics. Method Using the cytosine base editor BE3, single base editing vector OsALS171-SpG-eBE3 and OsALS190-SpG-eBE3 were constructed with ALS gene 171 and 190 as target sites. Gene edited plants were obtained through Agrobacterium mediated transformation method and target sites were genotyped with Sanger sequencing. A rapid herbicide tolerance system was established and tolerance level was identified in edited herbicide materials. Result Through T1 target sites sequencing, Two ALSP171Fmutant homozygous lines and one homozygous strain of ALSE187K R190H, ALSE187K, ALSV188I, ALSR190H, and ALSD201Nmutation types were obtained. Compared to wild-type material, Two ALSP171F mutant homozygous strains have strong tolerance to bispyribac-sodium(BS), while ALSE187K R190H, ALSE187K, ALSV188I, ALSR190H, and ALSD201Nmutant homozygous plants have some tolerances to BS, but the tolerance is not significant. Conclusion The gene edited materials can maintain stable inheritance, using the cytosine base editor BE3 to obtain materials with herbicide resistance characteristics, and the ALSP171Fmutation demonstrates strong resistance to bispyribac-sodium, which is a priority site for cultivating herbicide resistant rice.

Key words: rice, single base gene editing, herbicide-resistant, acetolactate synthase