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논문 기본 정보

자료유형
학술저널
저자정보
Roh, Kyung Hee (Department of Agricultural Biotechnology, National Academy of Agricultural Science, Rural Development Administration [RDA]) Choi, Soo Bok (Department of Agricultural Biotechnology, National Academy of Agricultural Science, Rural Development Administration [RDA]) Kang, Han-Chul (Department of Agricultural Biotechnology, National Academy of Agricultural Science, Rural Development Administration [RDA]) Kim, Jong-Bum (Department of Agricultural Biotechnology, National Academy of Agricultural Science, Rural Development Administration [RDA]) Kim, Hyun Uk (Department of Agricultural Biotechnology, National Academy of Agricultural Science, Rural Development Administration [RDA]) Lee, Kyeong-Ryeol (Department of Agricultural Biotechnology, National Academy of Agricultural Science, Rural Development Administration [RDA]) Kim, Sun Hee (Department of Agricultural Biotechnology, National Academy of Agricultural Science, Rural Development Administration [RDA])
저널정보
한국응용생명화학회 Applied Biological Chemistry Applied Biological Chemistry 제57권 제6호
발행연도
2014.1
수록면
759 - 768 (10page)

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The PISTILLATA is a floral organ identity gene required for the flower development. To gain a better understanding of the BnPI-1 promoter function, the promoter 5' deletion analysis was conducted, both in transgenic Brassica napus and transgenic Arabidopsis. In the ${\beta}$-glucuronidase (GUS) expression assay of transgenic B. napus, most of the 5' deletion constructs of the BnPI-1 promoter expressed the GUS gene strongly in all organs of the flower except the style, and deletion up to -326 bp region (removed up to the G-box located near the TATA-box) reduced dramatically the GUS expression, and deletion up to -150 bp region (removed up to the TATA-box) abolished the GUS expression. In the GUS fluorometric assay, GUS activity in the flower was about 4-fold higher than that in seed or silique, and GUS activity in the leaf was not detected. The GUS expression patterns in transgenic Arabidopsis were similar to those in transgenic B. napus. These results suggest that the BnPI-1 promoter can lead the foreign gene expression mainly in the floral-tissue, which is shown to be regulated by the G-box element responsive to basic leucine-zipper transcription factors.

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