Improved gateway binary vectors: High-performance vectors for creation of fusion constructs in Transgenic analysis of plants

被引:705
作者
Nakagawa, Tsuyoshi [1 ]
Suzuki, Takarnasa
Murata, Satoko
Nakamura, Shinya
Hino, Takeshi
Maeo, Kenichiro
Tabata, Ryo
Kawai, Tsutae
Tanaka, Katsunori
Niwa, Yasuo
Watanabe, Yuichiro
Nakamura, Kenzo
Kimura, Tetsuya
Ishiguro, Sumie
机构
[1] Shimane Univ, Ctr Integrated Res Sci, Dept Mol & Funct Genom, Matsue, Shimane 6908504, Japan
[2] Nagoya Univ, Grad Sch Bioagr Sci, Dept Biol Funct & Mech, Nagoya, Aichi 4648601, Japan
[3] Shimane Univ, Fac Life & Environm Sci, Dept Appl Biosci & Biotechnol, Matsue, Shimane 6908504, Japan
[4] Univ Shizuoka, Grad Sch Nutr & Environm Sci, Lab Plant Cell Technol, Shizuoka 4228526, Japan
[5] Univ Tokyo, Grad Sch Arts & Sci, Dept Life Sci, Tokyo 1538902, Japan
[6] Mie Univ, Fac Bioresources, Dept Sustainable Resource Sci, Tsu, Mie 5148507, Japan
关键词
binary vector; gateway cloning; reporter; tag;
D O I
10.1271/bbb.70216
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
We made a series of improved Gateway binary vectors (pGWBs) for plant transformation. Fifteen different reporters and tags, sGFP, GUS, LUC, EYFP, ECFP, G3GFP, mRFP, 6xHis, FLAG, 3xHA, 4xMyc, 10xMyc, GST, T7, and TAP, were employed. Some vectors carry the 2x35S-Omega promoter for higher-level expression. The kanamycin- and hygromycin-resistant markers are independently available for each of the 43 types of vectors, thus an additional transformation of once- transformed plants can be carried out easily. Their small size and high-copy number in Escherichia coli make possible easier handling at plasmid preparation and sequencing. Improved pGWBs should be a powerful tool for transgenic research in plants.
引用
收藏
页码:2095 / 2100
页数:6
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