首页> 外文期刊>Plant Cell, Tissue and Organ Culture: An International Journal on in Vitro Culture of Higher Plants >Determination of genomic location and structure of the transgenes in marker-free rice-based cholera vaccine by using whole genome resequencing approach
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Determination of genomic location and structure of the transgenes in marker-free rice-based cholera vaccine by using whole genome resequencing approach

机译:使用全基因组重测序方法确定无标记水稻基霍乱疫苗中转基因的基因组位置和结构

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We previously developed a molecularly uniform rice-based oral cholera vaccine (MucoRice-CTB) by using an overexpression system for modified cholera toxin B-subunit, CTB (N4Q) with RNAi to suppress production of the major rice endogenous storage proteins. To establish MucoRice-CTB for human use, here we developed hygromycin phosphotransferase selection marker-free MucoRice-CTB by using two different Agrobacterium tumefaciens, each carrying a distinct T-DNA for co-transformation. In the marker-free candidates from co-transformants by segregation in the seed progeny, we selected a line with high CTB expression, line 51A, which we advanced to the T6 generation by self-pollination to obtain a homozygous line without down-regulation of CTB expression. Southern blot analyses showed that three copies of the CTB gene, but not the backbone of the T-DNA binary vector, were inserted into the rice genome of MucoRice-CTB line 51A. By whole genome resequencing, we showed that the transgenes in this line were inserted into intergenic regions in chromosome 3 and chromosome 12. We determined that two full-length copies, each containing the CTB and RNAi expression cassettes, were inserted in a tandem reverted orientation into chromosome 3. An additional copy of the CTB over-expression cassette with a truncated RNAi cassette was inserted into chromosome 12. These findings provide useful information for the establishment of a seed bank of marker-free MucoRice-CTB for human use.
机译:我们以前通过使用带有RNA干扰的改良霍乱毒素B亚基CTB(N4Q)的过表达系统来开发分子均匀的基于水稻的口服霍乱疫苗(MucoRice-CTB),以抑制主要水稻内源性存储蛋白的产生。为了建立供人类使用的MucoRice-CTB,我们在这里开发了无潮霉素磷酸转移酶选择标记的MucoRice-CTB,方法是使用两种不同的根癌农杆菌,每一种携带不同的T-DNA进行共转化。在通过种子后代分离而来自共转化体的无标记候选物中,我们选择了具有高CTB表达的品系51A,我们通过自花传粉将其推进至T6世代以获得纯合品系,而无需下调CTB表达。 Southern印迹分析表明,将三份CTB基因而非T-DNA二元载体的骨架插入到MucoRice-CTB品系51A的水稻基因组中。通过全基因组重测序,我们显示了该品系中的转基因已插入3号染色体和12号染色体的基因间区域。我们确定了两个全长拷贝,每个拷贝均包含CTB和RNAi表达盒,并以串联回复的方向插入进入染色体3。将另一份带有截短的RNAi盒的CTB过表达盒插入到染色体12中。这些发现为建立供人类使用的无标记MucoRice-CTB种子库提供了有用的信息。

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