首页> 美国卫生研究院文献>Nucleic Acids Research >Isolation of telomeric DNA from the filamentous fungus Podospora anserina and construction of a self-replicating linear plasmid showing high transformation frequency.
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Isolation of telomeric DNA from the filamentous fungus Podospora anserina and construction of a self-replicating linear plasmid showing high transformation frequency.

机译:从丝状真菌Popospora anserina端粒DNA的分离和自复制线性质粒的构建显示出高转化频率。

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摘要

It has been previously shown that linear plasmids bearing Tetrahymena telomeric sequences are able to replicate autonomously in the filamentous fungus Podospora anserina (1). However, autonomous replication occurs in only 50-70% of the transformants, suggesting a defect in the recognition of the Tetrahymena telomeric template by the putative P. anserina telomerase so that only a fraction of entering DNA is stabilized into linear extrachromosomal molecules. We have cloned DNA sequences added to the Tetrahymena (T2G4)n ends of the linear plasmid. Nucleotide sequencing showed that these sequences are exclusively composed of T2AG3 repeat units. Hybridization experiments of Bal31 treated DNA showed that T2AG3 repeats are confined within 200 bp in chromosomal P. anserina telomeres. A new plasmid has been constructed so that after linearization, the terminal sequences contain T2AG3 repeats. This linear molecule transforms P. anserina with a high frequency (up to 1.75 x 10(4) transformants/micrograms), autonomous replication occurs in 100% of the transformants and the plasmid copy number is about 2-3 per nucleus. These results underscore the importance of the telomeric repeat nucleotide sequence for efficient recognition as functional telomeric DNA in vivo and provide the first step toward the development of an artificial chromosome cloning system for filamentous fungi.
机译:先前已证明带有四膜虫端粒序列的线性质粒能够在丝状真菌Podospora anserina(1)中自主复制。但是,仅50-70%的转化体会发生自主复制,这提示假定的P. anserina端粒酶对四膜虫端粒模板的识别存在缺陷,因此只有一小部分进入的DNA被稳定化为线性染色体外分子。我们已经克隆了添加到线性质粒四膜虫(T2G4)n末端的DNA序列。核苷酸测序表明,这些序列仅由T2AG3重复单元组成。 Bal31处理的DNA的杂交实验表明,T2AG3重复序列被限制在染色体P. anserina端粒的200 bp之内。已经构建了新质粒,以便在线性化后,末端序列包含T2AG3重复序列。该线性分子以高频率(高达1.75 x 10(4)个转化子/微克)转化鹅绒假单胞菌,自主复制发生在100%的转化子中,质粒拷贝数约为每个核2-3。这些结果强调了端粒重复核苷酸序列对于在体内有效识别为功能性端粒DNA的重要性,并为开发用于丝状真菌的人工染色体克隆系统迈出了第一步。

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