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改变四链体环 B 的鸟嘌呤碱基会影响菌毛抗原变异。

Altering the Guanine Quadruplex Loop Bases Affects Pilin Antigenic Variation.

机构信息

Department of Microbiology-Immunology, Northwestern University Feinberg School of Medicine, Chicago, Illinois 60611, United States.

出版信息

Biochemistry. 2020 Mar 17;59(10):1104-1112. doi: 10.1021/acs.biochem.9b01038. Epub 2020 Feb 27.

Abstract

possesses a programmed recombination system that allows the bacteria to alter the major subunit of the type IV pilus, pilin or PilE. An alternate DNA structure known as a guanine quadruplex (G4) is required for pilin antigenic variation (pilin Av). The G-C base pairs within the G4 motif are required for pilin Av, but simple mutation of the loop bases does not affect pilin Av. We show that more substantial changes to the loops, in both size and nucleotide composition, with the core guanines unchanged, decrease or abrogate pilin Av. We investigated why these loop changes might influence the efficiency of pilin Av. RecA is a recombinase required for pilin Av that can bind the G4 in vitro. RecA binds different G4 structures with altered loops with varied affinities. However, changes in RecA binding affinities to the loop mutants do not absolutely correlate with the pilin Av phenotypes. Interestingly, the yeast RecA ortholog, Rad51, also binds the G4 structure with a higher affinity than it binds single-stranded DNA, suggesting that RecA G4 binding is conserved in eukaryotic orthologs. The thermal stability the G4 structure and its loop mutants showed that the parental G4 structure had the highest melting temperature, and the melting temperature of the loop mutants correlated with pilin Av phenotype. These results suggest that the folding kinetics and stability of G4 structures are important for the efficiency of pilin Av.

摘要

它拥有一个程序化的重组系统,使细菌能够改变 IV 型菌毛的主要亚基,菌毛或 PilE。菌毛抗原变异(pilin Av)需要一种称为鸟嘌呤四联体(G4)的替代 DNA 结构。G4 模体中的 G-C 碱基对是 pilin Av 所必需的,但环碱基的简单突变不会影响 pilin Av。我们表明,环的大小和核苷酸组成发生更大的变化,而核心鸟嘌呤不变,会降低或消除 pilin Av。我们研究了为什么这些环的变化可能会影响 pilin Av 的效率。RecA 是 pilin Av 所必需的重组酶,它可以在体外结合 G4。RecA 可以结合具有不同亲和力的具有改变环的不同 G4 结构。然而,RecA 结合亲和力的变化与环突变体并不完全相关 pilin Av 表型。有趣的是,酵母 RecA 同源物 Rad51 也以比与单链 DNA 结合更高的亲和力结合 G4 结构,这表明 RecA G4 结合在真核同源物中是保守的。G4 结构及其环突变体的热稳定性表明,亲本 G4 结构具有最高的熔点,并且环突变体的熔点与 pilin Av 表型相关。这些结果表明 G4 结构的折叠动力学和稳定性对于 pilin Av 的效率很重要。

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