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Insertion mutagenesis and study of transposable elements using a new unstable virescent seedling allele for isolation of haploid petunia lines

机译:插入诱变和转座因子的研究使用新的不稳定的绿化幼苗​​等位基因分离单倍体矮牵牛线

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摘要

The new unstable virescent seedling (vis*) allele of a petunia mutant, that has green leaves but white cotyledons with green revertant spots, was used to identify spontaneously occurring haploid petunia lines with active transposable elements. Endogenous transposons were trapped into the single petunia nitrate reductase structural gene (nia) using chlorate selection on haploid protoplasts. In two mutant lines, the dTph1-like transposable element dTph1-3 was inserted at almost the same position but in opposite orientations in the first exon of the nia gene. In a third mutant, a different transposable element was integrated into the fourth exon. This element, called dTph4 is 787 bp long and has 13 bp terminal inverted repeats of which 12 bp are identical to those of dTph1. Insertion of dTph1-3 and dTph4 results in an 8 bp duplication of the target site, as already described for dTph1. In contrast to dTph1-like elements, dTph4 is present at low copy number in the petunia genome. This can facilitate its use for gene tagging in petunia. The dTph1-3 and dTph4 elements excise frequently, as transposon footprints were found in most of the insertion mutants. The data demonstrate that haploid petunia is an excellent system for gene tagging and for the study of transposable elements.
机译:矮牵牛突变体的新的不稳定的绿苗(vis *)等位基因,具有绿色的叶子,但白色的子叶带有绿色的可逆斑点,用于鉴定具有活性转座因子的自发出现的单倍体矮牵牛系。使用单倍体原生质体上的氯酸盐选择,将内源转座子捕获到单一的矮牵牛硝酸还原酶结构基因(nia)中。在两个突变株中,将dTph1样转座元件dTph1-3插入nia基因的第一个外显子中几乎相同的位置,但方向相反。在第三突变体中,将不同的转座元件整合到第四外显子中。这个称为dTph4的元件长787 bp,具有13 bp的末端反向重复序列,其中12 b​​p与dTph1相同。如dTph1所述,插入dTph1-3和dTph4会导致目标位点重复8 bp。与dTph1样元件相反,矮牵牛基因组中dTph4以低拷贝数存在。这可以促进其在矮牵牛中进行基因标记。 dTph1-3和dTph4元素频繁切除,因为在大多数插入突变体中都发现了转座子足迹。数据表明,单倍体矮牵牛是用于基因标记和研究转座因子的出色系统。

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