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Inhibition of Binding of Tomato Yellow Leaf Curl Virus Rep to its Replication Origin by Artificial Zinc-Finger Protein
被引:27
作者:
Mori, Tomoaki
[1
,2
]
Takenaka, Kosuke
[1
]
Domoto, Fumiya
[1
]
Aoyama, Yasuhiro
[1
,3
]
Sera, Takashi
[1
,2
]
机构:
[1] Kyoto Univ, Grad Sch Engn, Dept Synthet Chem & Biol Chem, Nishikyo Ku, Kyoto 6158510, Japan
[2] Okayama Univ, Grad Sch Nat Sci & Technol, Dept Appl Chem & Biotechnol, Kita Ku, Okayama 7008530, Japan
[3] Doshisha Univ, Fac Sci & Engn, Dept Mol Chem & Biochem, Kyotanabe, Kyoto 6100321, Japan
关键词:
Artificial zinc-finger protein;
Common region;
Geminivirus;
Replication-associated protein;
Tomato yellow leaf curl virus;
Virus replication;
GEMINIVIRUS REPLICATION;
DNA-REPLICATION;
SEQUENCE;
DESIGN;
D O I:
10.1007/s12033-012-9552-5
中图分类号:
Q5 [生物化学];
Q7 [分子生物学];
学科分类号:
071010 ;
081704 ;
摘要:
Previously we demonstrated that inhibition of replication-associated protein (Rep) binding to its replication origin by artificial zinc-finger proteins (AZPs) is a powerful method to prevent plant virus infection in vivo. In the present study, we applied the AZP technology to Tomato yellow leaf curl virus (TYLCV), which is a limiting factor in tomato cultivation worldwide. First, we determined 5'-ATCGGTGT ATCGGTGT-3' in the 195-bp intergenic region of the TYLCV-Israel strain, a strain reported first among TYLCV strains, as the Rep-binding site by gel shift assays. We then constructed a 6-finger AZP that bound to a 19-bp DNA including the Rep-binding site. We demonstrated that the binding affinity of the AZP was > 1,000-fold greater than that of Rep and that the AZP inhibited Rep binding completely in vitro. Because the binding capability of the AZP was same as that of the AZP previously designed for geminivirus-resistant Arabidopsis thaliana, we predict that the present AZP will prevent TYLCV infection in vivo.
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页码:198 / 203
页数:6
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