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pJan25 载体系列:对 Gateway 兼容载体 pGWB533 的增强,以扩大启动子测试应用。

The pJan25 vector series: an enhancement of the Gateway-compatible vector pGWB533 for broader promoter testing applications.

机构信息

Genetics Department, Faculty of Agriculture, Zagazig University, Egypt.

出版信息

Plasmid. 2013 May;69(3):249-56. doi: 10.1016/j.plasmid.2013.01.005. Epub 2013 Jan 23.

Abstract

Agrobacterium-mediated transformation of plants has enhanced our ability to progress more rapidly in plant genetic engineering. Development of binary vectors for Agrobacterium has played a major role in advancing plant biology. Here, we report new features added to the Gateway-compatible vector pGWB533 for promoter testing with the reporter gene encoding β-glucuronidase (GUS). The original vector contains the spectinomycin/streptomycin adenylyltransferase (aadA) gene for bacterial selection and the hygromycin phosphotransferase gene (hpt) for transformed plant selection. However, some bacterial strains used to transform plants, such as Agrobacterium rhizogenes strain K599, have elevated tolerance to spectinomycin and streptomycin, thus making bacterial selection of pGWB533 inefficient. Although pGWB533 confers chemical selection for transgenic plants using hygromycin resistance, the plasmid has no visual marker that enables visual selection of transformed plants or transgenic tissue. In this regard, adding a gene to constitutively express green fluorescent protein (eGFP) makes it easier to visually select the transformed tissue and trim out the non-transformed. In this report we describe a series of vectors, pJan25S (NCBI: KC416200), pJan25T (NCBI: KC416201) and pJan25X (NCBI: KC416202), that are enhancements of pGWB533 for promoter testing. All three vectors contain the gene encoding eGFP as a visual marker for transformed tissue. However, in pJan25S and pJan25T, eGFP is controlled by the rolD promoter for root-specific expression, while in pJan25X it is controlled by the CaMV35S promoter for constitutive expression in all plant tissues. Spectinomycin and streptomycin resistance remains in pJan25S for bacterial selection; however, pJan25T and pJan25X contain the gene encoding tetracycline resistance (tet) for bacterial selection. These changes resulted in enhanced vectors with better visual and chemical selection that should have broad application in promoter studies.

摘要

农杆菌介导的植物转化提高了我们在植物遗传工程中快速发展的能力。用于农杆菌的二元载体的发展在推进植物生物学方面发挥了重要作用。在这里,我们报告了为使用编码β-葡糖苷酸酶(GUS)的报告基因进行启动子测试而添加到 Gateway 兼容载体 pGWB533 的新功能。原始载体包含用于细菌选择的壮观霉素/链霉素腺苷转移酶(aadA)基因和用于转化植物选择的潮霉素磷酸转移酶基因(hpt)。然而,一些用于转化植物的细菌菌株,如根癌农杆菌 K599 菌株,对壮观霉素和链霉素的耐受性提高,从而使 pGWB533 的细菌选择效率降低。尽管 pGWB533 利用潮霉素抗性赋予转化植物的化学选择,但该质粒没有可视标记,无法用于转化植物或转化组织的可视选择。在这方面,添加一个基因来组成型表达绿色荧光蛋白(eGFP)使得更容易直观地选择转化组织并修剪出非转化的组织。在本报告中,我们描述了一系列载体,pJan25S(NCBI:KC416200)、pJan25T(NCBI:KC416201)和 pJan25X(NCBI:KC416202),它们是用于启动子测试的 pGWB533 的增强型载体。这三个载体都包含编码 eGFP 的基因,作为转化组织的可视标记。然而,在 pJan25S 和 pJan25T 中,eGFP 受 rolD 启动子控制,用于根特异性表达,而在 pJan25X 中,它受 CaMV35S 启动子控制,用于所有植物组织的组成型表达。壮观霉素和链霉素抗性仍保留在 pJan25S 中用于细菌选择;然而,pJan25T 和 pJan25X 包含编码四环素抗性(tet)的基因,用于细菌选择。这些变化导致了具有更好的视觉和化学选择的增强型载体,它们应该在启动子研究中有广泛的应用。

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