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  1. 50 大学院生物資源学研究科・生物資源学部
  2. 50A 学術雑誌論文
  3. 学術雑誌論文

Development of series of gateway binary vectors, pGWBs, for realizing efficient construction of fusion genes for plant transformation

http://hdl.handle.net/10076/10256
http://hdl.handle.net/10076/10256
1520f362-64bb-4876-8cf0-ca042471831b
名前 / ファイル ライセンス アクション
50A8603.pdf 本文 (3.1 MB)
Item type 学術雑誌論文 / Journal Article(1)
公開日 2009-07-13
タイトル
タイトル Development of series of gateway binary vectors, pGWBs, for realizing efficient construction of fusion genes for plant transformation
言語 en
言語
言語 eng
資源タイプ
資源タイプ識別子 http://purl.org/coar/resource_type/c_6501
資源タイプ journal article
著者 Nakagawa, Tsuyoshi

× Nakagawa, Tsuyoshi

en Nakagawa, Tsuyoshi

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Kurose, Takayuki

× Kurose, Takayuki

en Kurose, Takayuki

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Hino, Takeshi

× Hino, Takeshi

en Hino, Takeshi

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Tanaka, Katsunori

× Tanaka, Katsunori

en Tanaka, Katsunori

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Kawamukai, Makoto

× Kawamukai, Makoto

en Kawamukai, Makoto

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Niwa, Yasuo

× Niwa, Yasuo

en Niwa, Yasuo

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Toyooka, Kiminori

× Toyooka, Kiminori

en Toyooka, Kiminori

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Matsuoka, Ken

× Matsuoka, Ken

en Matsuoka, Ken

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Jinbo, Tetsuro

× Jinbo, Tetsuro

en Jinbo, Tetsuro

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Kimura, Tetsuya

× Kimura, Tetsuya

en Kimura, Tetsuya

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抄録
内容記述タイプ Abstract
内容記述 We developed a new series of binary vectors useful for Gateway cloning to facilitate transgenic experiments in plant biotechnology. The new system, Gateway Binary Vectors (pGWBs) realized efficient cloning, constitutive expression using the cauliflower mosaic virus (CaMV) 35S promoter and the construction of fusion genes by simple clonase reaction with an entry clone. The reporters employable in this system are GUS, sGFP, LUC, EYFP, and ECFP. The tags available are 6xHis, FLAG, 3xHA, 4xMyc, 10xMyc, GST, T7-epitope, and tandem affinity purification (TAP). In total, 13 kinds of reporter or tag were arranged and were almost applicable to both N- and C-fusions. The pGWBs could be used for many purposes, such as promoter::reporter analysis, observation of subcellular localization by the expression of proteins fused to a reporter or tag, and analysis of protein-protein interaction by copurification and immunodetection experiments. The pGWBs were constructed with modified pBI101 containing a CaMV35S promoter-driven hygromycin phosphotransferase (HPT) gene as the second selection marker. We also constructed pGWBs with the marker HPT driven by the nopaline synthase promoter. By using the pGWB system, the expression of tagged proteins, and the localization of GFP-fused proteins were easily analyzed. Moreover, tissue-specific and inducible gene expression using a promoter was also monitored with pGWBs. It is expected that, the pGWB system will serve as a powerful tool for plasmid construction in plant research.
書誌情報 Journal of bioscience and bioengineering

巻 104, 号 1, p. 34-41, 発行日 2007-07-25
ISSN
収録物識別子タイプ PISSN
収録物識別子 1389-1723
書誌レコードID
収録物識別子タイプ NCID
収録物識別子 AA11307678
フォーマット
内容記述タイプ Other
内容記述 application/pdf
著者版フラグ
出版タイプ AM
出版タイプResource http://purl.org/coar/version/c_ab4af688f83e57aa
日本十進分類法
主題Scheme NDC
主題 471
出版者
出版者 Society for Bioscience and Bioengineering, Japan
資源タイプ(三重大)
値 Journal Article / 学術雑誌論文
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