首页> 美国卫生研究院文献>Nucleic Acids Research >Cis-acting requirements in flanking DNA for the programmed elimination of mse2.9: a common mechanism for deletion of internal eliminated sequences from the developing macronucleus of Tetrahymena thermophila
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Cis-acting requirements in flanking DNA for the programmed elimination of mse2.9: a common mechanism for deletion of internal eliminated sequences from the developing macronucleus of Tetrahymena thermophila

机译:顺式要求 侧翼DNA中通过程序消除mse2.9:一种常见机制 用于从发育中删除内部消除的序列 嗜热四膜虫大核

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摘要

During macronuclear development in the ciliated protozoan Tetrahymena thermophila, extensive DNA deletions occur, eliminating thousands of internal eliminated sequences (IESs). Using an rDNA-based transformation assay we have analyzed the role during DNA deletion of DNA flanking mse2.9, an IES within the second intron of a gene encoding an as yet incompletely characterized protein. We establish that a cis-acting sequence for mse2.9 deletion acts at a distance to specify deletion boundaries. A complex sequence element necessary for efficient and accurate mse2.9 deletion is located in the region 47–81 bp from the right side of mse2.9. The ability of a variety of IES flanking sequences to rescue a processing deficient mse2.9 construct indicates that some cis-acting signal is shared among different IESs. In addition, the short intronic sequence that flanks mse2.9 is able to direct efficient and accurate processing. Despite no obvious sequence similarity between mse2.9 and other IESs, we suggest that a common mechanism is used to delete different families of IESs in Tetrahymena.
机译:在纤毛虫原生膜四膜虫的大核发育过程中,发生了广泛的DNA缺失,消除了数千个内部消除的序列(IES)。使用基于rDNA的转化分析,我们已经分析了侧翼mse2.9的DNA的DNA缺失过程中的作用,mse2.9是编码尚未完全表征的蛋白质的基因的第二个内含子中的IES。我们确立了mse2.9缺失的顺式作用序列在指定缺失边界的距离上起作用。有效和准确删除mse2.9所必需的复杂序列元素位于mse2.9右侧47-81 bp的区域中。各种IES侧翼序列抢救加工缺陷的mse2.9构建体的能力表明,不同IES之间共享一些顺式作用信号。此外,位于mse2.9旁的简短内含子序列能够指导高效而准确的处理。尽管mse2.9与其他IES之间没有明显的序列相似性,但我们建议使用一种通用机制删除四膜虫中不同的IES家族。

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