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利用CRISPR/Cas9系统定向编辑水稻SD1基因
引用本文:胡雪娇,杨佳,程灿,周继华,牛付安,王新其,张美良,曹黎明,储黄伟.利用CRISPR/Cas9系统定向编辑水稻SD1基因[J].中国水稻科学,2018,32(3):219-225.
作者姓名:胡雪娇  杨佳  程灿  周继华  牛付安  王新其  张美良  曹黎明  储黄伟
作者单位:1.上海市农业科学院作物育种栽培研究所, 上海 201403;2.江西农业大学农学院, 南昌 330045;3.上海海洋大学食品学院, 上海 201306
基金项目:上海市科技兴农重点攻关计划资助项目(沪农科攻字2014第7-1-2号);上海市浦江人才计划资助项目(16PJ1408900);上海市种业发展计划资助项目(沪农科种字2016第1-3号)。
摘    要:【目的】半矮秆水稻品种的选育和应用是水稻育种的最重大成果之一。半矮秆品种大多是半矮秆基因SD1(semi-dwarf1)功能缺失突变体,为了获得sd1突变体,本研究对SD1基因进行了定向编辑。【方法】利用CRISPR/Cas9系统,以SD1基因为靶基因,构建基因编辑载体CRISPR-SD1,用农杆菌介导的方法转化水稻恢复系申繁17和申繁24。【结果】在2个转化受体的T0代均获得了纯合的sd1突变体,并且在T1代株系中分离出了不含转基因序列的植株。2个品种的sd1突变体与各自的野生型相比,株高分别下降了25%左右。【结论】利用CRISPR/Cas9系统可以有效地对目的基因进行编辑,在水稻分子育种领域具有巨大的应用价值。

关 键 词:CRISPR/Cas9  基因编辑  水稻  半矮秆基因  
收稿时间:2017-09-04
修稿时间:2017-12-27

Targeted Editing of Rice SD1 Gene Using CRISPR/Cas9 System
HU Xuejiao,YANG Jia,CHENG Can,ZHOU Jihua,NIU Fuan,WANG Xinqi,ZHANG Meiliang,CAO Liming,CHU Huangwei.Targeted Editing of Rice SD1 Gene Using CRISPR/Cas9 System[J].Chinese Journal of Rice Science,2018,32(3):219-225.
Authors:HU Xuejiao  YANG Jia  CHENG Can  ZHOU Jihua  NIU Fuan  WANG Xinqi  ZHANG Meiliang  CAO Liming  CHU Huangwei
Institution:1.Institute of Crop Breeding and Cultivation, Shanghai Academy of Agricultural Sciences, Shanghai 201403, China;2.School of Agricultural Sciences, Jiangxi Agricultural University, Nanchang 330045,China;3.College of Food Sciences & Technology, Shanghai Ocean University, Shanghai 201306, China;
Abstract:【Objective】In the last century, the usage of semi-dwarf rice varieties brought about significant improvements and great achievements in rice breeding. Most of the semi-dwarf rice varieties have loss-of-function mutations in the Semi-Dwarf1 (SD1) gene. In order to obtain sd1 mutant, targeted editing of SD1 gene was performed. 【Method】SD1 gene editing vector CRISPR-SD1 was constructed by using CRISPR/Cas9 system, and transformed into two rice restore lines Shenfan 17 and Shenfan 24 by the Agrobacterium-mediated method.【Result】 Homozygous sd1 mutants were obtained in T0 generation in both varieties, and vector-free sd1 mutant lines were segregated from the T1 population. The plant heights of the two sd1 mutants were decreased by 25% as compared with those of their wild types. 【Conclusion】CRISPR/Cas9 is a powerful tool for rice target gene editing, and has enormous potential in rice molecular breeding.
Keywords:CRISPR/Cas9  gene editing  rice  Semi-Dwarf1  
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