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松弛酶 TrwC 中的转位基序特异性影响其由其接合型 IV 型分泌系统募集。

A translocation motif in relaxase TrwC specifically affects recruitment by its conjugative type IV secretion system.

机构信息

Departamento de Biología Molecular, Universidad de Cantabria, and IBBTEC, UC-SODERCAN-CSIC, Santander, Spain.

出版信息

J Bacteriol. 2013 Nov;195(22):4999-5006. doi: 10.1128/JB.00367-13. Epub 2013 Aug 30.

DOI:10.1128/JB.00367-13
PMID:23995644
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3811593/
Abstract

Type IV secretion system (T4SS) substrates are recruited through a translocation signal that is poorly defined for conjugative relaxases. The relaxase TrwC of plasmid R388 is translocated by its cognate conjugative T4SS, and it can also be translocated by the VirB/D4 T4SS of Bartonella henselae, causing DNA transfer to human cells. In this work, we constructed a series of TrwC variants and assayed them for DNA transfer to bacteria and human cells to compare recruitment requirements by both T4SSs. Comparison with other reported relaxase translocation signals allowed us to determine two putative translocation sequence (TS) motifs, TS1 and TS2. Mutations affecting TS1 drastically affected conjugation frequencies, while mutations affecting either motif had only a mild effect on DNA transfer rates through the VirB/D4 T4SS of B. henselae. These results indicate that a single substrate can be recruited by two different T4SSs through different signals. The C terminus affected DNA transfer rates through both T4SSs tested, but no specific sequence requirement was detected. The addition of a Bartonella intracellular delivery (BID) domain, the translocation signal for the Bartonella VirB/D4 T4SS, increased DNA transfer up to 4% of infected human cells, providing an excellent tool for DNA delivery to specific cell types. We show that the R388 coupling protein TrwB is also required for this high-efficiency TrwC-BID translocation. Other elements apart from the coupling protein may also be involved in substrate recognition by T4SSs.

摘要

IV 型分泌系统(T4SS)底物通过一个易位信号被招募,而该信号在共轭松弛酶中定义较差。质粒 R388 的松弛酶 TrwC 由其同源共轭 T4SS 易位,也可由巴尔通体的 VirB/D4 T4SS 易位,导致 DNA 转移到人类细胞。在这项工作中,我们构建了一系列 TrwC 变体,并对其进行了细菌和人类细胞 DNA 转移的测定,以比较两种 T4SS 的募集要求。与其他报道的松弛酶易位信号的比较使我们能够确定两个假定的易位序列(TS)基序,TS1 和 TS2。影响 TS1 的突变极大地影响了接合频率,而影响任一基序的突变对通过 B. henselae 的 VirB/D4 T4SS 的 DNA 转移率只有轻微影响。这些结果表明,单个底物可以通过两个不同的 T4SS 通过不同的信号被募集。C 末端影响通过两种测试的 T4SS 的 DNA 转移率,但未检测到特定的序列要求。添加巴尔通体细胞内递呈(BID)结构域,即巴尔通体 VirB/D4 T4SS 的易位信号,可将 DNA 转移率提高至感染人类细胞的 4%,为特定细胞类型的 DNA 转移提供了极好的工具。我们表明,R388 偶联蛋白 TrwB 也需要这种高效的 TrwC-BID 易位。除了偶联蛋白之外的其他元件也可能参与 T4SS 对底物的识别。

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