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同源重组是丝状子囊菌棉阿舒囊霉中DNA整合的主要机制及重排的原因。

Homologous recombination as the main mechanism for DNA integration and cause of rearrangements in the filamentous ascomycete Ashbya gossypii.

作者信息

Steiner S, Wendland J, Wright M C, Philippsen P

机构信息

Institut für Mikrobiologie und Molekularbiologie, Justus-Liebig-Universität, Giessen, Germany.

出版信息

Genetics. 1995 Jul;140(3):973-87. doi: 10.1093/genetics/140.3.973.

Abstract

A slow and a fast growth phenotype were observed after transformation of the phytopathogenic fungus Ashbya gossypii using a plasmid carrying homologous DNA and as selectable marker the Tn903 aminoglycoside resistance gene expressed from a strong A. gossypii promoter. Transformations with circular plasmids yielded slowly and irregularly growing geneticin-resistant mycelia in which 1% of nuclei contained plasmid sequences. Occasionally, fast growing sectors appeared which were shown to be initiated by homologous integration of the transforming DNA. Transformants obtained with plasmids linearized within the homology region immediately exhibited fast radial growth. In all 28 transformants analyzed plasmid DNA was integrated homologously. Such apparent lack of nonhomologous recombination has so far not been observed in filamentous ascomycetes. In 14 transformants two to four tandemly integrated plasmid copies were found. They underwent several types of genetic changes, mainly in the older mycelium: excision of whole plasmid copies and rearrangements within the integrated DNA (inversions and deletions). These internal rearrangements involved 360-bp inverted repeats, remnants of IS-elements flanking the resistance gene, and 156-bp direct repeats, originating from the strong A. gossypii promoter. Improved vectors lacking sequence repetitions were constructed and used for stable one-step gene replacement in A. gossypii.

摘要

用携带同源DNA的质粒转化植物病原真菌棉阿舒囊霉,并以由强棉阿舒囊霉启动子表达的Tn903氨基糖苷抗性基因作为选择标记后,观察到了一种缓慢生长和一种快速生长的表型。用环状质粒转化产生了生长缓慢且不规则的对遗传霉素有抗性的菌丝体,其中1%的细胞核含有质粒序列。偶尔会出现快速生长的扇形区域,经证明是由转化DNA的同源整合引发的。用在同源区域内线性化的质粒获得的转化体立即表现出快速的径向生长。在分析的所有28个转化体中,质粒DNA都是同源整合的。迄今为止,在丝状子囊菌中尚未观察到这种明显缺乏非同源重组的情况。在14个转化体中发现了两到四个串联整合的质粒拷贝。它们经历了几种类型的遗传变化,主要发生在较老的菌丝体中:整个质粒拷贝的切除以及整合DNA内的重排(倒位和缺失)。这些内部重排涉及360 bp的反向重复序列、抗性基因侧翼IS元件的残余部分以及156 bp的正向重复序列,后者源自强棉阿舒囊霉启动子。构建了缺乏序列重复的改良载体,并用于棉阿舒囊霉的稳定一步基因替换。

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本文引用的文献

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