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IS1384是从恶臭假单胞菌H菌株新发现的一种插入序列,其反向重复序列是IS1383整合的特异性靶点。

The inverted repeats of IS1384, a newly described insertion sequence from Pseudomonas putida strain H, represent the specific target for integration of IS1383.

作者信息

Müller C, Lauf U, Hermann H

机构信息

Institut für Genetik und Biochemie, Ernst-Moritz-Arndt-Universität Greifswald, Germany.

出版信息

Mol Genet Genomics. 2001 Aug;265(6):1004-10. doi: 10.1007/s004380100495.

Abstract

Analysis of a region on plasmid pPGH1 from Pseudomonas putida strain H that is flanked by two copies of IS1383 has revealed an additional element with the typical features of a bacterial insertion sequence. This new IS element, designated IS1384, contains a single ORF of 972 bp, and is flanked by 9-bp inverted repeats. Based on sequence homology and structural characteristics of the putative transposase it encodes, IS1384 belongs to the IS5 subgroup of the IS5 family. Two copies of IS1384 are present on plasmid pPGH1, whereas none could be detected on the chromosome of P. putida strain H. Sequence analysis revealed the presence of two truncated copies of IS1384 on the second plasmid in this strain, pPGH2. The inverted repeats of all IS1384 copies (including the truncated ones) are interrupted by the integration of an IS1383 element. All integrations were found to be site- and orientation-specific. PCR studies and sequence data indicate that IS1383 can form a circular intermediate on excision. In the circular form, the previously described 13-bp inverted repeats of IS1383 are separated by 10 bp that are identical to the 5-bp motif that flanks each side of the element when it is integrated in its target. We provide evidence that these additional nucleotides, although not of inverted symmetry, represent an essential part of the inverted repeats. Furthermore, the data indicate that IS1383 integrated into the inverted repeats of IS1384 by a site-specific recombination rather than a site-specific insertion event.

摘要

对恶臭假单胞菌H菌株的质粒pPGH1上一个由两个IS1383拷贝侧翼包围的区域进行分析,发现了一个具有典型细菌插入序列特征的额外元件。这个新的IS元件被命名为IS1384,它包含一个972 bp的单一开放阅读框,并由9 bp的反向重复序列侧翼包围。基于其编码的假定转座酶的序列同源性和结构特征,IS1384属于IS5家族的IS5亚组。质粒pPGH1上存在两个IS1384拷贝,而在恶臭假单胞菌H菌株的染色体上未检测到。序列分析显示该菌株的第二个质粒pPGH2上存在两个截短的IS1384拷贝。所有IS1384拷贝(包括截短的拷贝)的反向重复序列都被一个IS1383元件的整合打断。所有整合都是位点和方向特异性的。PCR研究和序列数据表明,IS1383在切除时可以形成一个环状中间体。在环状形式中,先前描述的IS1383的13 bp反向重复序列被10 bp隔开,这10 bp与该元件整合到其靶标时两侧的5 bp基序相同。我们提供的证据表明,这些额外的核苷酸虽然不是反向对称的,但却是反向重复序列的重要组成部分。此外,数据表明IS1383是通过位点特异性重组而不是位点特异性插入事件整合到IS1384的反向重复序列中的。

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