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The nicking homing endonuclease I-BasI is encoded by a group I intron in the DNA polymerase gene of the Bacillus thuringiensis phage Bastille

机译:刻痕归巢内切核酸酶I-BasI由苏云金芽孢杆菌噬菌体巴士底狱DNA聚合酶基因中的I组内含子编码

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摘要

Here we describe the discovery of a group I intron in the DNA polymerase gene of Bacillus thuringiensis phage Bastille. Although the intron insertion site is identical to that of the Bacillus subtilis phages SPO1 and SP82 introns, the Bastille intron differs from them substantially in primary and secondary structure. Like the SPO1 and SP82 introns, the Bastille intron encodes a nicking DNA endonuclease of the H-N-H family, I-BasI, with a cleavage site identical to that of the SPO1-encoded enzyme I-HmuI. Unlike I-HmuI, which nicks both intron-minus and intron-plus DNA, I-BasI cleaves only intron-minus alleles, which is a characteristic of typical homing endonucleases. Interestingly, the C-terminal portions of these H-N-H phage endonucleases contain a conserved sequence motif, the intron-encoded endonuclease repeat motif (IENR1) that also has been found in endonucleases of the GIY-YIG family, and which likely comprises a small DNA-binding module with a globular ββααβ fold, suggestive of module shuffling between different homing endonuclease families.
机译:在这里,我们描述了苏云金芽孢杆菌噬菌体巴士底狱的DNA聚合酶基因中的第I组内含子的发现。尽管内含子的插入位点与枯草芽孢杆菌噬菌体SPO1和SP82内含子相同,但巴士底狱的内含子在一级和二级结构上却大不相同。像SPO1和SP82内含子一样,巴士底狱内含子编码H-N-H家族I-BasI的切口DNA核酸内切酶,其切割位点与SPO1编码的酶I-HmuI相同。 I-HmuI会切割内含子-负向和内含子-正向DNA,而I-BasI只能切割内含子-负向等位基因,这是典型归巢内切核酸酶的特征。有趣的是,这些HNH噬菌体核酸内切酶的C端部分包含一个保守的序列基序,即内含子编码的核酸内切酶重复基序(IENR1),也已在GIY-YIG家族的核酸内切酶中发现,并且可能包含一个小的DNA-球状ββααβ折叠的结合模块,提示不同归巢核酸内切酶家族之间的模块改组。

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