...
首页> 外文期刊>Plasmid: An International Journal Devoted to Extrachromosomal Gene Systems >The pJan25 vector series: An enhancement of the Gateway-compatible vector pGWB533 for broader promoter testing applications
【24h】

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

机译:pJan25载体系列:网关兼容载体pGWB533的增强,可用于更广泛的启动子测试应用

获取原文
获取原文并翻译 | 示例
           

摘要

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.
机译:农杆菌介导的植物转化增强了我们在植物基因工程中进展更快的能力。农杆菌二元载体的开发在促进植物生物学中发挥了重要作用。在这里,我们报告了添加到网关兼容载体pGWB533中的新功能,用于使用编码β-葡萄糖醛酸苷酶(GUS)的报告基因进行启动子测试。原始载体包含用于细菌选择的壮观霉素/链霉素腺苷酸转移酶(.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,例如发根农杆菌菌株K599,对壮观霉素和链霉素的耐受性升高,从而使pGWB533的细菌选择效率低下。尽管pGWB533赋予了使用潮霉素抗性的转基因植物化学选择,但该质粒没有视觉标记,可以目视选择转化植物或转基因组织。在这方面,添加一个基因组成性表达绿色荧光蛋白(eGFP),可以更容易地从视觉上选择转化的组织并修剪掉未转化的组织。在本报告中,我们介绍了一系列载体pJan25S(NCBI:KC416200), pJan25T(NCBI:KC416201)和pJan25X(NCBI:KC416202),是用于启动子测试的pGWB533的增强。所有这三个载体都包含编码eGFP的基因,作为转化组织的视觉标记。但是,在pJan25S和pJan25T中,eGFP受rolD启动子控制以进行根特异性表达,而在pJan25X中,其受CaMV35S启动子控制以在所有植物组织中进行组成型表达。 pJan25S中仍然存在对壮观霉素和链霉素的耐药性,以进行细菌选择。但是,pJan25T和pJan25X包含编码细菌选择的四环素抗性(。tet)的基因。这些变化导致增强的载体具有更好的视觉和化学选择,应在启动子研究中广泛应用。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号