甘藍基因轉移之研究(一)基因鎗轉移法
Other Title
Studies on Gene Transfer Into Cabbage (Brassica oleracea L. var. capitata) (Ⅰ) Airgun Transfer
Journal
中國園藝
Journal Volume
38
Journal Issue
4
Pages
214-227
Date Issued
1992-12
Date
1992
Author(s)
許家言
曾夢蛟
尤進欽
張武男
Jia-Yan Hsu
Menq-Jiau Tseng
Jin-Chin Yiu
Woo-Nang Chang
Abstract
本研究以甘藍爲材料，利用基因鎗轉移的方法，將GUS報導基因轉移到甘藍，並以轉殖後之GUS基因表現的活性爲依據，探討轉移之適當條件。試驗結果顯示，基因鎗轉移GUS基因到甘藍原生質體，以氣室真空度在200 mmHg，2.25×10^5原生質體(150µl)爲最適宜。轉移至甘藍組織以胚及莖頂分生組織爲材料較佳，設定氣室真空度爲600 mmHg、鎗口至檔板關距離爲4公分，取5至10µl(1µg/µl)的環狀DNA，扣板機一次，鎗擊五個胚，可得至最佳的轉移效果。基因鎗轉移不同質體的效率，以基因小者較佳。利用基因鎗轉移基因到甘藍成熟胚，是一種簡便、快速分析基因暫時表現的方法。但轉殖的胚會隨組織發育逐漸消失GUS活性，顯示GUS基因並非穩定嵌入甘藍的染色體。
The objective of this study is to establish an optimal condition of airgun transformation system for cabbage (Brassica oleracea L. var. capitata) by GUS reporter gene, Results indicated that setting the chamber pressure at 200 mmHg, and applied 150 µ1 of cabbage protoplasts (2.25 × 10^5) was the best condition for airgun transformation. The highest level(l00%) of transient GUS gene expression were observed both in the mature embryo and shoot meristem when the transformations ware conducted at the following conditions, i. e., the distance between stopping plate and material is set at 4 cm, chamber vacuum is at 600 mmHg and using circular plasmids. The expression of GUS activity was decreased drastically since 6 days after transformation indicated that the expression of GUS gene was not due to the stable integration but only a transient gene expression.
Subjects
甘藍
基因鎗
基因轉移
cabbage
airgun
gene transfer
Publisher
臺灣園藝學會
Type
journal article
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