SGI1 excludes IncA and IncC plasmids

IF 1.8 4区 生物学 Q3 GENETICS & HEREDITY
Stephanie J. Ambrose, Ruth M. Hall
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引用次数: 0

Abstract

SGI1 and its many variant forms are integrative mobilizable elements that rely on IncA or IncC plasmids for transfer functions. However, the coexistence of SGI1 with the plasmid is unstable in the longer term. Here, we have investigated the effect of SGI1 type integrative elements on the initial entry of these plasmids. Using two transfer proficient IncC plasmids and the IncA plasmid RA1, exclusion indices were 40–100-fold for SGI1-I or SGI1-D which have a complete backbone. Using the SGI1-K and SGI1-LK1 variants that lack backbone segments, loss of a region of 5793 bp that includes the traHG transfer genes and the downstream open reading frame S010 was found to abolish exclusion. S010 was shown to be co-transcribed with traHG and hence also under the control of an AcaDC inducible promoter. However, complementation with a 5.2 kbp fragment that included the traHG-S010 operon did not restore exclusion activity to SGI1-LK1. Part of S013 that encodes a small polypeptide of unknown function, was also lost from SGI1-LK1. S013 and the adjacent S014 gene were also co-transcribed. However complementation with S013-S014 did not restore exclusion activity to SGI1-LK1. Hence, the precise cause of the SGI1-mediated plasmid exclusion remains elusive.
SGI1不包括IncA和IncC质粒。
SGI1及其许多变体形式是依赖IncA或IncC质粒实现传递功能的综合可移动元件。然而,从长期来看,SGI1与质粒的共存是不稳定的。在这里,我们研究了SGI1型整合元件对这些质粒初始进入的影响。使用两种转染熟练的IncC质粒和IncA质粒RA1,对具有完整主干的SGI1-I或SGI1-D的排除指数为40-100倍。使用缺乏主干片段的SGI1-K和SGI1-LK1变异,发现5793 bp区域的丢失,包括traHG转移基因和下游开放阅读框S010,消除了排除。S010被证明与traHG共转录,因此也受到AcaDC诱导启动子的控制。然而,与包含trag - s010操纵子的5.2 kbp片段互补并不能恢复SGI1-LK1的排除活性。S013编码一种功能未知的小多肽的部分基因也从SGI1-LK1中丢失。S013和相邻的S014基因也共转录。然而,与S013-S014的互补并不能恢复SGI1-LK1的排除活性。因此,sgi1介导的质粒排斥的确切原因仍然难以捉摸。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Plasmid
Plasmid 生物-遗传学
CiteScore
4.70
自引率
3.80%
发文量
21
审稿时长
53 days
期刊介绍: Plasmid publishes original research on genetic elements in all kingdoms of life with emphasis on maintenance, transmission and evolution of extrachromosomal elements. Objects of interest include plasmids, bacteriophages, mobile genetic elements, organelle DNA, and genomic and pathogenicity islands.
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