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Genome-Wide Analysis of a TaLEA-Introduced Transgenic Populus simonii × Populus nigra Dwarf Mutant

机译:TaLEA导入的转基因西杨×黑杨矮化突变体的全基因组分析

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摘要

A dwarf mutant (dwf1) was obtained among 15 transgenic lines, when TaLEA (Tamarix androssowii late embryogenesis abundant gene) was introduced into Populus simonii × Populus nigra by Agrobacterium tumefaciens-mediated transformation. Under the same growth conditions, dwf1 height was significantly reduced compared with the wild type and the other transgenic lines. Because only one transgenic line (dwf1) displayed the dwarf phenotype, we considered that T-DNA insertion sites may play a role in the mutant formation. The mechanisms underlying this effect were investigated using TAIL-PCR (thermal asymmetric interlaced PCR) and microarrays methods. According to the TAIL-PCR results, two flanking sequences located on chromosome IV and VIII respectively, were cloned. The results indicated the integration of two independent T-DNA copies. We searched for the potential genes near to the T-DNA insertions. The nearest gene was a putative poplar AP2 transcription factor (GI: 224073210). Expression analysis showed that AP2 was up-regulated in dwf1 compared with the wild type and the other transgenic lines. According to the microarrays results, a total of 537 genes involved in hydrolase, kinase and transcription factor activities, as well as protein and nucleotide binding, showed significant alterations in gene expression. These genes were expressed in more than 60 metabolic pathways, including starch, sucrose, galactose and glycerolipid metabolism and phenylpropanoids and flavonoid biosyntheses. Our transcriptome and T-DNA insertion sites analyses might provide some useful insights into the dwarf mutant formation.
机译:通过根癌农杆菌介导的转化将TaLEA(Tamarix androssowii晚胚发生丰富基因)引入到Populus simonii×Populus nigra中,在15个转基因品系中获得了矮化突变体(dwf1)。在相同的生长条件下,与野生型和其他转基因品系相比,dwf1高度显着降低。因为只有一个转基因品系(dwf1)显示出矮表型,所以我们认为T-DNA插入位点可能在突变体形成中起作用。使用TAIL-PCR(热不对称交错PCR)和微阵列方法研究了这种作用的潜在机制。根据TAIL-PCR结果,克隆了分别位于IV和VIII染色体上的两个侧翼序列。结果表明两个独立的T-DNA副本的整合。我们搜索了接近T-DNA插入的潜在基因。最近的基因是推定的杨树AP2转录因子(GI:224073210)。表达分析表明,与野生型和其他转基因品系相比,dwf1中的AP2上调。根据微阵列结果,涉及水解酶,激酶和转录因子活性以及蛋白质和核苷酸结合的总共537个基因显示出基因表达的显着改变。这些基因在60多个代谢途径中表达,包括淀粉,蔗糖,半乳糖和甘油脂代谢以及苯丙烷和类黄酮的生物合成。我们的转录组和T-DNA插入位点分析可能会提供一些有用的见解,以矮化突变体的形成。

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