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Tagging and Cloning of a Petunia Flower Color Gene with the Maize Transposable Element Activator.

机译:带有玉米转座因子激活子的矮牵牛花色基因的标签和克隆。

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摘要

We report here the use of the maize transposable element Activator (Ac) to isolate a dicot gene. Ac was introduced into petunia, where it transposed into Ph6, one of several genes that modify anthocyanin pigmentation in flowers by affecting the pH of the corolla. Like other Ac-mutable alleles, the new mutation is unstable and reverts to a functional form in somatic and germinal tissues. The mutant gene was cloned using Ac as a probe, demonstrating the feasibility of heterologous transposon tagging in higher plants. Confirmation that the cloned DNA fragment corresponded to the mutated gene was obtained from an analysis of revertants. In every case examined, reversion to the wild-type phenotype was correlated with restoration of a wild-type-sized DNA fragment. New transposed Acs were detected in many of the revertants. As in maize, the frequency of somatic and germinal excision of Ac from the mutable allele appears to be dependent on genetic background.
机译:我们在此报告了玉米转座子激活因子(Ac)的使用,以分离双子叶植物基因。 Ac被引入矮牵牛,然后被转化为Ph6,Ph6是通过影响花冠的pH来修饰花中花色苷色素的几种基因之一。像其他Ac可变等位基因一样,新突变是不稳定的,并在体细胞和生发组织中恢复为功能形式。使用Ac作为探针克隆了突变基因,证明了在高等植物中进行异源转座子标签的可行性。通过对回复株的分析,确认克隆的DNA片段对应于突变的基因。在所检查的每种情况下,回复至野生型表型均与恢复野生型大小的DNA片段相关。在许多回复株中检测到新的转座Acs。与玉米一样,从可变等位基因中去除Ac的体细胞和发芽的频率似乎取决于遗传背景。

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