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Engineering a family of synthetic splicing ribozymes.

机译:设计一个合成拼接核酶家族。

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Controlling RNA splicing opens up possibilities for the synthetic biologist. The Tetrahymena ribozyme is a model group I self-splicing ribozyme that has been shown to be useful in synthetic circuits. To create additional splicing ribozymes that can function in synthetic circuits, we generated synthetic ribozyme variants by rationally mutating the Tetrahymena ribozyme. We present an alignment visualization for the ribozyme termed as structure information diagram that is similar to a sequence logo but with alignment data mapped on to secondary structure information. Using the alignment data and known biochemical information about the Tetrahymena ribozyme, we designed synthetic ribozymes with different primary sequences without altering the secondary structure. One synthetic ribozyme with 110 nt mutated retained 12% splicing efficiency in vivo. The results indicate that our biochemical understanding of the ribozyme is accurate enough to engineer a family of active splicing ribozymes with similar secondary structure but different primary sequences.
机译:控制RNA剪接为合成生物学家开辟了可能性。四膜虫核酶是一种I型自粘核酶,已被证明可用于合成回路。为了创建可以在合成电路中起作用的其他拼接核酶,我们通过合理地突变四膜虫核酶来生成合成核酶变体。我们提出了核糖核酸的比对可视化,称为结构信息图,类似于序列徽标,但比对数据映射到二级结构信息上。使用关于四膜虫核酶的比对数据和已知的生化信息,我们设计了具有不同一级序列而不改变二级结构的合成核酶。一种具有110 nt突变的合成核酶在体内保留了12%的剪接效率。结果表明,我们对核酶的生化理解足够准确,可以设计出具有类似二级结构但不同一级序列的活性剪接核酶家族。

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