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I-PfoP3I:一种新型的切口 HNH 归巢内切酶,编码于 Phormidium foveolarum 噬菌体 Pf-WMP3 的 DNA 聚合酶基因的内含子 I 中。

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.

机构信息

State Key Laboratory of Protein and Plant Gene Research, College of Life Sciences, Peking University, Beijing, China.

出版信息

PLoS One. 2012;7(8):e43738. doi: 10.1371/journal.pone.0043738. Epub 2012 Aug 27.

Abstract

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 Mg(2+), Ca(2+) or Mn(2+) 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.

摘要

除了一些游离的归巢内切核酸酶外,在噬藻体基因组中编码在蛋白质编码基因中的 I 类自我剪接内含子的归巢内切核酸酶尚未被报道。在这项研究中,描述了一种在 T7 样噬藻体 Pf-WMP3 的 DNA 聚合酶基因中 I 型 A2 内含子编码的切口 DNA 内切核酸酶 I-PfoP3I,该噬藻体感染淡水蓝藻 Phormidium foveolarum。Pf-WMP3 内含子在体内有效地剪接,并且在转录过程中同时自我剪接。I-PfoP3I 属于 HNH 家族,具有非常规的 C 末端 HNH 基序。I-PfoP3I 在体外比缺乏任何内含子的 Pf-WMP4 DNA 聚合酶基因更有效地切割内含子缺失的 Pf-WMP3 DNA 聚合酶基因,表明 I-PfoP3I 的可变能力。I-PfoP3I 在体外切割内含子缺失的 Pf-WMP3 和 Pf-WMP4 DNA 聚合酶基因的编码链上,在内含子插入位点的上游切割 4nt。使用体外切割测定法和无内含子靶位点的扫描缺失突变体,确定最小识别位点是切割位点下游的 14bp 区域。I-PfoP3I 需要 Mg(2+)、Ca(2+)或 Mn(2+)才能进行切口活性。系统发育分析表明,内含子和归巢内切核酸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,这是第一个报道在噬藻体基因组中蛋白质编码基因中的 I 类自我剪接内含子编码功能性归巢内切核酸酶的报告。

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