Agrobacterium-mediated transformation of monocot and dicot plants using the NCR promoter derived from soybean chlorotic mottle virus

被引:30
作者
Fukuoka, H
Ogawa, T
Mitsuhara, I
Iwai, T
Isuzugawa, K
Nishizawa, Y
Gotoh, Y
Nishizawa, Y
Tagiri, A
Ugaki, M
Ohshima, M
Yano, H
Murai, N
Niwa, Y
Hibi, T
Ohashi, Y
机构
[1] Natl Inst Agrobiol Resources, Tsukuba, Ibaraki 3058602, Japan
[2] Chugoku Natl Agr Expt Stn, Hiroshima 7218514, Japan
[3] Japan Sci & Technol Corp, CREST, Chiyoda Ku, Tokyo 1010062, Japan
[4] Yamagata Prefectural Hort Expt Stn, Yamagata 9910043, Japan
[5] Hokuriku Natl Agr Exptl Stn, Niigata 9430193, Japan
[6] Louisiana State Univ, Dept Plant Pathol & Crop Physiol, Baton Rouge, LA 70803 USA
[7] LSU Med Ctr, Baton Rouge, LA 70803 USA
[8] Univ Shizuoka, Grad Sch Nutr & Environm Sci, Shizuoka 4228526, Japan
[9] Univ Tokyo, Dept Agr & Environm Biol, Bunkyo Ku, Tokyo 1138657, Japan
关键词
soybean chlorotic mottle virus; Agrobacterium-mediated transformation; NCR promoter; transgenic rice; transgenic tobacco;
D O I
10.1007/s002990000191
中图分类号
Q94 [植物学];
学科分类号
071001 ;
摘要
The NCR promoter (PNCR) from soybean chlorotic mottle virus (SoyCMV) was used to express the selectable marker, neomycin phosphotransferase (nptII) gene, in Agrobacterium-mediated transformation of both monocot (rice) and dicot (tobacco) plants. A multi-cloning site for insertion of a gene of interest into the binary vector pTN is located proximal to the right border region of T-DNA. When chimeric genes under the control of other strong promoters were located in a head-to-head orientation to the PNCR-nptII gene, kanamycin-resistant tobacco shoots were generated more efficiently than when using the original pTN vectors. This suggests that the enhancer-like sequences in the promoters adjacent to PNCR may promote expression of the PNCR-nptII gene.
引用
收藏
页码:815 / 820
页数:6
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