Over-expression of putative transcriptional coactivator KELP interferes with Tomato mosaic virus cell-to-cell movement

被引:30
作者
Sasaki, Nobumitsu [1 ]
Ogata, Takuya [1 ]
Deguchi, Masakazu [1 ]
Nagai, Shoko [1 ]
Tamai, Atsushi [2 ]
Meshi, Tetsuo [3 ]
Kawakami, Shigeki [4 ]
Watanabe, Yuichiro [5 ]
Matsushita, Yasuhiko [1 ]
Nyunoya, Hiroshi [1 ]
机构
[1] Tokyo Univ Agr & Technol, Ctr Gene Res, Fuchu, Tokyo 1838509, Japan
[2] Ishikawa Prefectural Univ, Res Inst Bioresources & Biotechnol, Nonoichi, Ishikawa 9218836, Japan
[3] Natl Inst Agrobiol Sci, Div Plant Sci, Tsukuba, Ibaraki 3058602, Japan
[4] Osaka Univ, Grad Sch Engn, Frontier Res Ctr, Suita, Osaka 5650871, Japan
[5] Univ Tokyo, Grad Sch Arts & Sci, Dept Life Sci, Meguro Ku, Tokyo 1538902, Japan
基金
日本学术振兴会;
关键词
PROTEIN-KINASE; 30K PROTEIN; IN-VITRO; TOBACCO; LOCALIZATION; TOBAMOVIRUS; PHOSPHORYLATION; INFECTION; PLANTS; PLASMODESMATA;
D O I
10.1111/j.1364-3703.2008.00517.x
中图分类号
Q94 [植物学];
学科分类号
071001 ;
摘要
Tomato mosaic virus (ToMV) encodes a movement protein (MP) that is necessary for virus cell-to-cell movement. We have demonstrated previously that KELP, a putative transcriptional coactivator of Arabidopsis thaliana, and its orthologue from Brassica campestris can bind to ToMV MP in vitro. In this study, we examined the effects of the transient over-expression of KELP on ToMV infection and the intracellular localization of MP in Nicotiana benthamiana, an experimental host of the virus. In co-bombardment experiments, the over-expression of KELP inhibited virus cell-to-cell movement. The N-terminal half of KELP (KELPdC), which had been shown to bind to MP, was sufficient for inhibition. Furthermore, the over-expression of KELP and KELPdC, both of which were co-localized with ToMV MP, led to a reduction in the plasmodesmal association of MP. In the absence of MP expression, KELP was localized in the nucleus and the cytoplasm by the localization signal in its N-terminal half. It was also shown that ToMV amplified normally in protoplasts prepared from leaf tissue that expressed KELP transiently. These results indicate that over-expressed KELP interacts with MP in vivo and exerts an inhibitory effect on MP function for virus cell-to-cell movement, but not on virus amplification in individual cells.
引用
收藏
页码:161 / 173
页数:13
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