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在淋病奈瑟菌中进行的计算机基因组比较表明,丝状噬菌体通过其自身的转座酶进行整合。

Genome comparison in silico in Neisseria suggests integration of filamentous bacteriophages by their own transposase.

作者信息

Kawai Mikihiko, Uchiyama Ikuo, Kobayashi Ichizo

机构信息

Department of Medical Genome Sciences, Graduate School of Frontier Science, The University of Tokyo, Japan.

出版信息

DNA Res. 2005;12(6):389-401. doi: 10.1093/dnares/dsi021. Epub 2006 Feb 22.

DOI:10.1093/dnares/dsi021
PMID:16769696
Abstract

We have identified filamentous prophages, Nf (Neisserial filamentous phages), during an in silico genome comparison in Neisseria. Comparison of three genomes of Neisseria meningitidis and one of Neisseria gonorrhoeae revealed four subtypes of Nf. Eleven intact copies are located at different loci in the four genomes. Each intact copy of Nf is flanked by duplication of 5'-CT and, at its right end, carries a transposase homologue (pivNM/irg) of RNaseH/Retroviral integrase superfamily. The phylogeny of these putative transposases and that of phage-related proteins on Nfs are congruent. Following circularization of Nfs, a promoter-like sequence forms. The sequence at the junction of these predicted circular forms (5'-atCTtatat) was found in a related plasmid (pMU1) at a corresponding locus. Several structural variants of Nfs--partially inverted, internally deleted and truncated--were also identified. The partial inversion seems to be a product of site-specific recombination between two 5'-CTtat sequences that are in inverse orientation, one at its end and the other upstream of pivNM/irg. Formation of internally deleted variants probably proceeded through replicative transposition that also involved two 5'-CTtat sequences. We concluded that the PivNM/Irg transposase on Nfs integrated their circular forms into the chromosomal 5'-CT-containing sequences and probably mediated the above rearrangements.

摘要

我们在对奈瑟菌进行电子基因组比较的过程中,鉴定出了丝状原噬菌体Nf(奈瑟菌丝状噬菌体)。对3个脑膜炎奈瑟菌基因组和1个淋病奈瑟菌基因组的比较揭示了Nf的4个亚型。在这4个基因组的不同位点上存在11个完整拷贝。Nf的每个完整拷贝两侧都有5'-CT重复序列,并且在其右端携带一个属于RNaseH/逆转录病毒整合酶超家族的转座酶同源物(pivNM/irg)。这些推定转座酶的系统发育与Nfs上噬菌体相关蛋白的系统发育是一致的。Nfs环化后会形成一个类似启动子的序列。在相关质粒(pMU1)的相应位点发现了这些预测环状形式连接处的序列(5'-atCTtatat)。还鉴定出了Nfs的几种结构变体——部分倒置、内部缺失和截短。部分倒置似乎是两个反向的5'-CTtat序列之间位点特异性重组的产物,一个位于其末端,另一个位于pivNM/irg上游。内部缺失变体的形成可能是通过复制转座进行的,这也涉及两个5'-CTtat序列。我们得出结论,Nfs上的PivNM/Irg转座酶将其环状形式整合到染色体含5'-CT的序列中,并可能介导了上述重排。

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