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通过真空渗透将DNA直接导入完整植物组织中来实现外源基因的瞬时表达。

Transient expression of a foreign gene by direct incorporation of DNA into intact plant tissue through vacuum infiltration.

作者信息

Zhou Bo, Zhao Xia, Kawabata Saneyuki, Li Yuhua

机构信息

College of Life Science, Northeast Forestry University, 150040, Harbin, China.

出版信息

Biotechnol Lett. 2009 Nov;31(11):1811-5. doi: 10.1007/s10529-009-0080-8. Epub 2009 Jul 18.

Abstract

We previously established a method to induce transient expression of foreign genes in intact plant tissue to detect the subcellular localization of proteins. Here, we have inserted a putative bZIP protein HY5 gene (SeqID: EU386772), isolated from the seedlings of turnips Brassica rapa L. subsp. rapa 'Tsuda,' and a receptor-like kinase gene AtRLK (SeqID: AY531551.1), isolated from Arabidopsis, into the plasmid pA7-GFP. We accomplished the direct incorporation of DNA into onion epidermal tissue by vacuum infiltration. By detecting GFP, which was fused with AtRLK or putative BrHY5, we determined that BrHY5 is located in the nucleus and AtRLK is located in the plasma membrane. This approach can be thus used to study the transient expression of foreign genes in intact tissue.

摘要

我们之前建立了一种在完整植物组织中诱导外源基因瞬时表达以检测蛋白质亚细胞定位的方法。在此,我们将从芜菁油菜(Brassica rapa L. subsp. rapa 'Tsuda')幼苗中分离得到的一个假定的bZIP蛋白HY5基因(序列ID:EU386772)以及从拟南芥中分离得到的一个类受体激酶基因AtRLK(序列ID:AY531551.1)插入到质粒pA7-GFP中。我们通过真空渗透法实现了将DNA直接导入洋葱表皮组织。通过检测与AtRLK或假定的BrHY5融合的GFP,我们确定BrHY5定位于细胞核,AtRLK定位于质膜。因此,这种方法可用于研究完整组织中外源基因的瞬时表达。

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