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首页> 外文期刊>Nucleic Acids Research >Transposases are responsible for the target specificity of IS1397 and ISKpn1 for two different types of palindromic units (PUs)
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Transposases are responsible for the target specificity of IS1397 and ISKpn1 for two different types of palindromic units (PUs)

机译:转座酶负责IS1397和ISKpn1对两种不同类型回文单位(PU)的靶标特异性

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摘要

Insertion sequences (IS)1397 and ISKpn1, found in Escherichia coli and Klebsiella pneumoniae, respectively, are IS3 family members that insert specifically into short palindromic repeated sequences (palindromic units or PUs). In this paper, we first show that although PUs are naturally absent from extrachromosomal elements, both ISs are able to transpose from the chromosome or from a plasmid into PUs artificially introduced into target plasmids. We also show that ISKpn1 target specificity is restricted to K.pneumoniae Z~1 PU type, whereas IS1397 target specificity is less stringent since the IS targets the three E.coli Y, Z~1 and Z~2 PU types indifferently. Experiments of transposition of both ISs driven by both transposases demonstrate that the inverted repeats flanking the ISs are not responsible for this target specificity, which is entirely due to the transposase itself. Implications on ISs evolution are presented.
机译:分别在大肠杆菌和肺炎克雷伯菌中发现的插入序列(IS)1397和ISKpn1是IS3家族成员,它们专门插入短回文重复序列(回文单位或PU)中。在本文中,我们首先表明,虽然染色体外元件自然不存在PU,但两个IS都能够从染色体或质粒转座到人工引入目标质粒的PU中。我们还表明,ISKpn1靶标特异性仅限于肺炎克雷伯菌Z〜1 PU型,而IS1397靶标特异性则不那么严格,因为IS分别靶向三种大肠杆菌Y,Z〜1和Z〜2 PU型。由两个转座酶驱动的两个IS的转座实验表明,IS侧翼的反向重复序列与该靶标特异性无关,这完全归因于转座酶本身。提出了对ISs演变的启示。

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