The molecular breeding of the silkworm which make silk protein of different insect and the production of new fiber.
| Project/Area Number |
13460025
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| Research Category |
Grant-in-Aid for Scientific Research (B)
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| Allocation Type | Single-year Grants |
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| Section | 一般 |
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| Research Field |
蚕糸・昆虫利用学
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| Research Institution | Shinshu University |
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Principal Investigator |
NAKAGAKI Masao Shinshu University, Faculty of Textile Science and Technology, Professor, 繊維学部, 教授 (70135169)
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| Co-Investigator(Kenkyū-buntansha) |
KAJIURA Zenta Shinshu University, Faculty of Textile Science and Technology, Associate Professor, 繊維学部, 助教授 (10224403)
SHIOMI Kunihiro Shinshu University, Faculty of Textile Science and Technology, Assistant Professor, 繊維学部, 助手 (70324241)
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| Project Period (FY) |
2001 – 2004
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| Project Status |
Completed (Fiscal Year 2004)
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| Budget Amount *help |
¥15,300,000 (Direct Cost: ¥15,300,000)
Fiscal Year 2004: ¥2,700,000 (Direct Cost: ¥2,700,000)
Fiscal Year 2003: ¥2,700,000 (Direct Cost: ¥2,700,000)
Fiscal Year 2002: ¥2,700,000 (Direct Cost: ¥2,700,000)
Fiscal Year 2001: ¥7,200,000 (Direct Cost: ¥7,200,000)
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| Keywords | Molecular breeding / Silkworm / Spider / Transposone / Silk fibroin / トランスポゾン / 遺伝子ターゲッティング / バキュロウイルス |
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| Research Abstract |
The purpose of this study is to breed silkworms which spin silk of different insect species by genetic engineering and to construct system of more efficient breeding. For first two years, we have tried to creat the silkworm which spin spider silk using a baculovirus which does not kill silkworms as a transfer vector. However, we can make no transgenic silkworm by this method though we have experimented using many silkworms. Then, using system of piggyBac which was a DNA type transposon, we have done the germline transfer experiment of a gene of the spider silk, flagelliform silk, to chromosome DNA of silkworm. The flagelliform silk has a high stretchiness, and expands to the length of 3 times. Because a spider is eating meat, the mass breeding is difficult. A spider spins several kinds of silk. It is difficult for the spider to spin only the flagelliform silk. Then we thought that it is significant to make a silkworm which produces flagelliform silk. We have transferred the incomplete piggyBac, in which flagelliform silk gene was incorporated, into genome DNA of a silkworm, and we confirmed that the expressed flagelliform silk protein was included in a cocoon. The flagelliform silk gene which transferred into genome DNA of a silkworm can be maintained stably. However, the content of flagelliform silk protein in a cocoon made by the recombinant silkworm was only one or two% of total cocoon protein mass. a coming theme is to raise the ratio of the spider thread which the silkworm makes.
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Report
(5 results)
Research Products
(7 results)
