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I-PfoP3I: A Novel Nicking HNH Homing Endonuclease Encoded in the Group I Intron of the DNA Polymerase Gene in Phormidium foveolarum Phage Pf-WMP3

机译:I-pfop3I:一种新型泥炭截短HNH归巢内切核酸酶编码在席藻foveolarum噬菌体pF-Wmp3的DNa聚合酶基因的第I组内含子

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摘要

Homing endonucleases encoded in a group I self-splicing intron in a protein-coding gene in cyanophage genomes have not been reported, apart from some free-standing homing edonucleases. In this study, a nicking DNA endonuclease, I-PfoP3I, encoded in a group IA2 intron in the DNA polymerase gene of a T7-like cyanophage Pf-WMP3, which infects the freshwater cyanobacterium Phormidium foveolarum is described. The Pf-WMP3 intron splices efficiently in vivo and self-splices in vitro simultaneously during transcription. I-PfoP3I belongs to the HNH family with an unconventional C-terminal HNH motif. I-PfoP3I nicks the intron-minus Pf-WMP3 DNA polymerase gene more efficiently than the Pf-WMP4 DNA polymerase gene that lacks any intervening sequence in vitro, indicating the variable capacity of I-PfoP3I. I-PfoP3I cleaves 4 nt upstream of the intron insertion site on the coding strand of EXON 1 on both intron-minus Pf-WMP3 and Pf-WMP4 DNA polymerase genes. Using an in vitro cleavage assay and scanning deletion mutants of the intronless target site, the minimal recognition site was determined to be a 14 bp region downstream of the cut site. I-PfoP3I requires Mg2+, Ca2+ or Mn2+ for nicking activity. Phylogenetic analysis suggests that the intron and homing endonuclease gene elements might be inserted in Pf-WMP3 genome individually after differentiation from Pf-WMP4. To our knowledge, this is the first report of the presence of a group I self-splicing intron encoding a functional homing endonuclease in a protein-coding gene in a cyanophage genome.
机译:除了一些独立的归巢核酸外,还没有报道在氰基虫基因组中的蛋白质编码基因中的第一类自我剪接内含子中编码的归巢核酸内切酶。在这项研究中,描述了一个有切口的DNA核酸内切酶I-PfoP3I,它在T7样噬菌体Pf-WMP3的DNA聚合酶基因的IA2内含子中编码,该基因会感染淡水蓝藻小球藻。在转录过程中,Pf-WMP3内含子可在体内有效剪接,在体外可自我剪接。 I-PfoP3I属于HNH家族,具有非常规的C端HNH基序。 I-PfoP3I比缺少任何体外插入序列的Pf-WMP4 DNA聚合酶基因更有效地对内含子减去Pf-WMP3 DNA聚合酶基因进行切刻,表明I-PfoP3I的能力可变。 I-PfoP3I在内含子减去Pf-WMP3和Pf-WMP4 DNA聚合酶基因上均在EXON 1编码链的内含子插入位点上游切割4 nt。使用体外切割测定和无内含子目标位点的扫描缺失突变体,确定最小识别位点为切割位点下游的14 bp区域。 I-PfoP3I需要Mg 2 + ,Ca 2 + 或Mn 2 + 才能进行切刻。系统发育分析表明,内含子和归巢核酸内切酶基因元件可能在与Pf-WMP4分化后分别插入Pf-WMP3基因组中。据我们所知,这是首次报告在噬菌体基因组的蛋白质编码基因中存在编码功能性归巢核酸内切酶的I类自剪接内含子。

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