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Midcell Recruitment of the DNA Uptake and Virulence Nuclease EndA for Pneumococcal Transformation

机译:DNA摄取和毒力核酸酶EndA的中细胞招募用于肺炎球菌转化

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摘要

Genetic transformation, in which cells internalize exogenous DNA and integrate it into their chromosome, is widespread in the bacterial kingdom. It involves a specialized membrane-associated machinery for binding double-stranded (ds) DNA and uptake of single-stranded (ss) fragments. In the human pathogen Streptococcus pneumoniae, this machinery is specifically assembled at competence. The EndA nuclease, a constitutively expressed virulence factor, is recruited during competence to play the key role of converting dsDNA into ssDNA for uptake. Here we use fluorescence microscopy to show that EndA is uniformly distributed in the membrane of noncompetent cells and relocalizes at midcell during competence. This recruitment requires the dsDNA receptor ComEA. We also show that under ‘static’ binding conditions, i.e., in cells impaired for uptake, EndA and ComEA colocalize at midcell, together with fluorescent end-labelled dsDNA (Cy3-dsDNA). We conclude that midcell clustering of EndA reflects its recruitment to the DNA uptake machinery rather than its sequestration away from this machinery to protect transforming DNA from extensive degradation. In contrast, a fraction of ComEA molecules were located at cell poles post-competence, suggesting the pole as the site of degradation of the dsDNA receptor. In uptake-proficient cells, we used Cy3-dsDNA molecules enabling expression of a GFP fusion upon chromosomal integration to identify transformed cells as GFP producers 60–70 min after initial contact between DNA and competent cells. Recording of images since initial cell-DNA contact allowed us to look back to the uptake period for these transformed cells. Cy3-DNA foci were thus detected at the cell surface 10–11 min post-initial contact, all exclusively found at midcell, strongly suggesting that active uptake of transforming DNA takes place at this position in pneumococci. We discuss how midcell uptake could influence homology search, and the likelihood that midcell uptake is characteristic of cocci and/or the growth phase-dependency of competence.
机译:遗传转化是细菌界广泛存在的一种遗传转化,其中细胞将外源DNA内化并整合到其染色体中。它涉及专门的膜相关机器,用于结合双链(ds)DNA和摄取单链(ss)片段。在人类病原体肺炎链球菌中,这种机器是专门组装而成的。 EndA核酸酶是一种组成型表达的毒力因子,在竞争过程中被募集,起着将dsDNA转化为ssDNA进行摄取的关键作用。在这里,我们使用荧光显微镜显示EndA均匀分布在非感受态细胞的膜中,并在感受力过程中重新定位在中层细胞上。此募集需要dsDNA受体ComEA。我们还显示,在“静态”结合条件下,即在摄取受限的细胞中,EndA和ComEA与荧光末端标记的dsDNA(Cy3-dsDNA)一起位于中层细胞。我们得出的结论是,EndA的中细胞集群反应了其向DNA摄取机制的募集,而不是其从该机制的隔离,以保护转化的DNA免受广泛降解。相反,一部分ComEA分子在竞争后位于细胞极,表明该极是dsDNA受体降解的位点。在摄取能力强的细胞中,我们使用了Cy3-dsDNA分子,使它们能够在染色体整合后表达GFP融合蛋白,从而在DNA与感受态细胞最初接触后60–70分钟将转化细胞鉴定为GFP生产者。自从最初的细胞与DNA接触以来的图像记录使我们可以回顾这些转化细胞的吸收期。因此,在初次接触后10-11分钟就在细胞表面检测到了Cy3-DNA病灶,所有这些都仅在中层细胞中发现,强烈表明在肺炎球菌的此位置发生了主动摄取转化DNA。我们讨论中细胞摄取如何影响同源性搜索,以及中细胞摄取是球菌和/或能力的生长阶段依赖性的特征的可能性。

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