利用CRISPR/Cas9技术定向编辑水稻OsIAA11
李兆伟,零东兰,孙聪颖,曾慧玲,刘凯基,蓝颖珊,范凯,林文雄

CRISPR/Cas9 Targeted Editing of OsIAA11 in Rice
LI ZhaoWei,LING DongLan,SUN CongYing,ZENG HuiLing,LIU KaiJi,LAN YingShan,FAN Kai,LIN WenXiong
表1 所用的引物序列
Table 1 The primer sequences used in this study
引物名称Primer name 引物序列Primer sequence (5′-3′) 用途Usage
OsIAA11-T1-fwd gccgCGCGCGGCTTGTCGGGATC 靶序列1构建
Construction of target site 1
OsIAA11-T1-rev aaacGATCCCGACAAGCCGCGCG
OsIAA11-T2-fwd gttgAGCTACCCGGAGTTGTCCA 靶序列2构建
Construction of target site 2
OsIAA11-T2-rev aaacTGGACAACTCCGGGTAGCT
Hyp-F ACGGTGTCGTCCATCACAGTTTGCC T0代阳性转基因植株鉴定
Identification of the T0 positive transgenic plant
Hyp-R TTCCGGAAGTGCTTGACATTGGGGA
OsIAA11-T1-F AGACCATCGACCTCAAGC 靶点1测序检测
Sequencing for target 1
OsIAA11-T1-R GCTAACTAATGGCTCTTC
OsIAA11-T2-F GACGATGATGTCAACTTT 靶点2测序检测
Sequencing for target 2
OsIAA11-T2-R GATAATGGTAGAATAACTCA
Hyp-T2-F CTATTTCTTTGCCCTCGGAC T2代纯合突变植株体内潮霉素基因检测
Detection of the gene encoded for hygromycin in the T2 homozygous mutations
Hyp-T2-R GACGTCTGTCGAGAAGTTTCTG