新型 ISCR 元件 ISCR28 捕捉 armA。

IF 4.9 2区 医学 Q1 INFECTIOUS DISEASES
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引用次数: 0

摘要

ISCR28 是 IS91 类插入序列家族中功能齐全的活性成员。ISCR28 长 1,708 bp,包含一个长 1,293 bp 的推测开放阅读框,编码一个转座酶。从 GenBank 中提取的 60 个含有 ISCR28 的序列产生了 27 个非重复的遗传背景,所有这些都代表了在多种革兰氏阴性生物中自然发生的生物事件。将 ISCR28 插入目标 DNA 时,需要在其 terIS(复制终止子)末端存在 5'-GXXT-3' 序列。其 oriIS(复制源)前 4 bp 的缺失可能导致 ISCR28 被困在基于 ISApl1 的转座子或类似结构中。terIS 的缺失以及与上游移动元件的融合可能促进了 ISCR28 和下游抗性基因的共同转移。ArmA 及其下游完整的 ISCR28 可从重组 pKD46 质粒中切除,形成环状中间体,进一步阐明了其作为转座酶的活性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Capture of armA by a novel ISCR element, ISCR28

ISCR28 is a fully functional and active member of the IS91-like family of insertion sequences. ISCR28 is 1,708-bp long and contains a 1,293-bp long putative open reading frame that codes a transposase. Sixty ISCR28-containing sequences from GenBank generated 27 non-repeat genetic contexts, all of which represented naturally occurring biological events that had occurred in a wide range of gram-negative organisms. Insertion of ISCR28 into target DNA preferred the presence of a 5′-GXXT-3′ sequence at its terIS (replication terminator) end. Loss of the first 4 bp of its oriIS (origin of replication) likely caused ISCR28 to be trapped in ISApl1-based transposons or similar structures. Loss of terIS and fusion with a mobile element upstream likely promoted co-transfer of ISCR28 and the downstream resistance genes. ArmA and its downstream intact ISCR28 can be excised from recombinant pKD46 plasmids forming circular intermediates, further elucidating its activity as a transposase.

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来源期刊
CiteScore
21.60
自引率
0.90%
发文量
176
审稿时长
36 days
期刊介绍: The International Journal of Antimicrobial Agents is a peer-reviewed publication offering comprehensive and current reference information on the physical, pharmacological, in vitro, and clinical properties of individual antimicrobial agents, covering antiviral, antiparasitic, antibacterial, and antifungal agents. The journal not only communicates new trends and developments through authoritative review articles but also addresses the critical issue of antimicrobial resistance, both in hospital and community settings. Published content includes solicited reviews by leading experts and high-quality original research papers in the specified fields.
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